ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Pathway network for the ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

Sources:

WikiPathways
R&D Systems

Pathways in the ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

#	Name	Source	Genes
1	ncRNAs involved in Wnt signaling in hepatocellular carcinoma	WikiPathways	APC AXIN1 CCND1 CCND2 CCND3 CER1 CHD8 CSNK1A1 CSNK1A1L CSNK1E CSNK2A1 CSNK2A2 CSNK2A3 CSNK2B CTBP1 CTBP2 CTNNB1 CTNNBIP1 CXXC4 DKK1 DKK2 DKK4 DVL1 DVL2 DVL3 ELAVL1 EZH2 FOSL1 FRAT1 FRAT2 FZD1 FZD10 FZD2 FZD3 FZD5 FZD6 FZD7 FZD8 FZD9 GSK3B JUN KLF4 KREMEN1 LEF1 LRP5 LRP6 MIR18A MIR320A MIR452 MTDH MYC NKD1 NKD2 NLK NOTUM PLAU PORCN ROR1 ROR2 RYK SENP2 SERPINF1 SFRP1 SFRP2 SFRP4 SFRP5 SOST SOX17 SOX7 TCF7 TCF7L1 TCF7L2 WIF1 WNT1 WNT10A WNT10B WNT11 WNT16 WNT2 WNT2B WNT3 WNT3A WNT4 WNT5A WNT5B WNT6 WNT7A WNT7B (see all 88) (see less)
2	Wnt Signaling Pathways	R&D Systems	APC AXIN1 AXIN2 BCL9 BCL9L BTRC CAMK2A CAMK2B CAMK2D CAMK2G CSNK1A1 CSNK1D CSNK1E CSNK1G1 CTNNB1 DAAM1 DVL1 DVL2 DVL3 FZD1 FZD10 FZD2 FZD3 FZD4 FZD5 FZD6 FZD7 FZD8 FZD9 GPC1 GPC2 GPC3 GPC5 GPC6 GSK3A GSK3B LEF1 LGR4 LGR5 LGR6 LRP5 LRP6 MAP3K7 MAPK10 MAPK8 MAPK9 NFATC1 NFATC2 NFATC3 NFATC4 NLK PLCB1 PLCB2 PLCB3 PLCB4 PPP3CA PPP3R1 PRKCA PRKCB PRKCD PRKCE PRKCG PRKCI PRKCQ PRKCZ PRKD1 PYGO1 PYGO2 RAC1 RAC2 RAC3 RHOA RHOB RHOC ROCK1 ROCK2 ROR1 ROR2 RSPO1 RSPO2 RSPO3 RSPO4 RYK SDC1 SDC2 SDC3 SDC4 SRC TCF7 TCF7L1 TCF7L2 TLE1 TLE2 TLE3 TLE4 TLE5 TLE6 WNT1 WNT10A WNT10B WNT11 WNT2 WNT2B WNT3A WNT4 WNT5A WNT5B WNT6 WNT7A WNT7B WNT8A WNT8B WNT9A WNT9B (see all 114) (see less)
3	Wnt signaling	WikiPathways	APC AXIN1 CAMK2A CAMK2B CAMK2D CAMK2G CCND1 CCND2 CCND3 CER1 CHD8 CSNK1A1 CSNK1A1L CSNK1E CSNK2A1 CSNK2A2 CSNK2A3 CSNK2B CTBP1 CTBP2 CTNNB1 CTNNBIP1 CXXC4 DAAM1 DAAM2 DKK1 DKK2 DKK4 DVL1 DVL2 DVL3 FOSL1 FRAT1 FRAT2 FZD1 FZD10 FZD2 FZD3 FZD5 FZD6 FZD7 FZD8 FZD9 GPC4 GSK3B INVS JUN KREMEN1 LEF1 LOC105372522 LRP5 LRP6 MAP3K7 MAPK8 MAPK9 MYC NFATC1 NFATC2 NFATC3 NFATC4 NKD1 NKD2 NLK NOTUM PLAU PLCB2 PLCB3 PLCB4 PORCN PPP3CA PPP3CB PPP3CC PPP3R1 PPP3R2 PRICKLE1 PRICKLE2 PRKCA PRKCB PRKCG RAC1 RHOA ROCK2 ROR1 ROR2 RYK SENP2 SERPINF1 SFRP1 SFRP2 SFRP4 SFRP5 SOST SOX17 TCF7 TCF7L1 TCF7L2 VANGL1 VANGL2 WIF1 WNT1 WNT10A WNT10B WNT11 WNT16 WNT2 WNT2B WNT3 WNT3A WNT4 WNT5A WNT5B WNT6 WNT7A WNT7B (see all 114) (see less)
4	Wnt signaling pathway and pluripotency	WikiPathways	APC AXIN1 AXIN2 CCND1 CCND2 CCND3 CD44 CREBBP CSNK1E CTBP1 CTBP2 CTNNB1 CTNND1 DVL1 DVL2 DVL3 EP300 ESRRB FBXW2 FOSL1 FOXD3 FRAT1 FZD1 FZD10 FZD2 FZD3 FZD4 FZD5 FZD6 FZD7 FZD8 FZD9 GSK3B JUN LDLR LEF1 LRP5 LRP6 LRRK2 MAP2K4 MAP3K7 MAPK10 MAPK9 MMP7 MYC NANOG NFYA NKD1 NKD2 NLK PAFAH1B1 PLAU POU5F1 PPARD PPM1J PPP2CA PPP2CB PPP2R1A PPP2R1B PPP2R2A PPP2R2B PPP2R2C PPP2R3A PPP2R3B PPP2R5C PPP2R5E PRKCA PRKCB PRKCD PRKCE PRKCG PRKCH PRKCI PRKCQ PRKCZ PRKD1 PTPA RACGAP1 RHOA SOX2 TCF7 TCF7L1 TCF7L2 TP53 WNT1 WNT10A WNT10B WNT11 WNT16 WNT2 WNT2B WNT3 WNT3A WNT4 WNT5A WNT5B WNT6 WNT7A WNT7B WNT9B ZBTB33 (see all 101) (see less)
5	lncRNA in canonical Wnt signaling and colorectal cancer	WikiPathways	APC APC2 ATF3 AXIN1 AXIN2 CCND1 CCND2 CCND3 CDK6 CDK8 CER1 CHD8 CSNK1A1 CSNK1A1L CSNK1E CSNK2A1 CSNK2A2 CSNK2A3 CSNK2B CTBP1 CTBP2 CTNNB1 CTNNBIP1 CXXC4 DKK1 DKK2 DKK4 DVL1 DVL2 DVL3 EZH2 FOSL1 FRAT1 FRAT2 FZD1 FZD10 FZD2 FZD3 FZD5 FZD6 FZD7 FZD8 FZD9 GSK3B H19 HNRNPK HNRNPU JUN KREMEN1 LEF1 LRP5 LRP6 MACROH2A2 MAP3K7 MIR16-1 MIR16-2 MIR34AHG MYC NKD1 NKD2 NLK NOTUM PLAU PORCN ROR1 ROR2 RUVBL1 RYK SENP2 SERPINF1 SFRP1 SFRP2 SFRP4 SFRP5 SOST SOX17 TCF3 TCF7 TCF7L1 TCF7L2 TFAP2A WIF1 WNT1 WNT10A WNT10B WNT11 WNT16 WNT2 WNT2B WNT3 WNT3A WNT4 WNT5A WNT5B WNT6 WNT7A WNT7B (see all 97) (see less)

Gene overlap in member pathways for ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

#	Symbol	Description	Category	# Related Pathways
1	WNT3A	Wnt Family Member 3A	Protein Coding	5
2	TCF7L1	Transcription Factor 7 Like 1	Protein Coding	5
3	FZD8	Frizzled Class Receptor 8	Protein Coding	5
4	FZD6	Frizzled Class Receptor 6	Protein Coding	5
5	AXIN1	Axin 1	Protein Coding	5
6	WNT5B	Wnt Family Member 5B	Protein Coding	5
7	WNT10A	Wnt Family Member 10A	Protein Coding	5
8	WNT2B	Wnt Family Member 2B	Protein Coding	5
9	WNT11	Wnt Family Member 11	Protein Coding	5
10	WNT10B	Wnt Family Member 10B	Protein Coding	5
11	WNT7A	Wnt Family Member 7A	Protein Coding	5
12	WNT5A	Wnt Family Member 5A	Protein Coding	5
13	WNT2	Wnt Family Member 2	Protein Coding	5
14	WNT1	Wnt Family Member 1	Protein Coding	5
15	TCF7L2	Transcription Factor 7 Like 2	Protein Coding	5
16	TCF7	Transcription Factor 7	Protein Coding	5
17	WNT4	Wnt Family Member 4	Protein Coding	5
18	LEF1	Lymphoid Enhancer Binding Factor 1	Protein Coding	5
19	LRP5	LDL Receptor Related Protein 5	Protein Coding	5
20	LRP6	LDL Receptor Related Protein 6	Protein Coding	5
21	APC	APC Regulator Of Wnt Signaling Pathway	Protein Coding	5
22	GSK3B	Glycogen Synthase Kinase 3 Beta	Protein Coding	5
23	FZD2	Frizzled Class Receptor 2	Protein Coding	5
24	DVL3	Dishevelled Segment Polarity Protein 3	Protein Coding	5
25	DVL1	Dishevelled Segment Polarity Protein 1	Protein Coding	5
26	CTNNB1	Catenin Beta 1	Protein Coding	5
27	DVL2	Dishevelled Segment Polarity Protein 2	Protein Coding	5
28	CSNK1E	Casein Kinase 1 Epsilon	Protein Coding	5
29	FZD10	Frizzled Class Receptor 10	Protein Coding	5
30	FZD9	Frizzled Class Receptor 9	Protein Coding	5
31	FZD7	Frizzled Class Receptor 7	Protein Coding	5
32	FZD1	Frizzled Class Receptor 1	Protein Coding	5
33	FZD3	Frizzled Class Receptor 3	Protein Coding	5
34	FZD5	Frizzled Class Receptor 5	Protein Coding	5
35	WNT7B	Wnt Family Member 7B	Protein Coding	5
36	WNT6	Wnt Family Member 6	Protein Coding	5
37	NLK	Nemo Like Kinase	Protein Coding	5
38	CCND3	Cyclin D3	Protein Coding	4
39	CCND2	Cyclin D2	Protein Coding	4
40	WNT3	Wnt Family Member 3	Protein Coding	4
41	RYK	Receptor Like Tyrosine Kinase	Protein Coding	4
42	CCND1	Cyclin D1	Protein Coding	4
43	PLAU	Plasminogen Activator, Urokinase	Protein Coding	4
44	ROR2	Receptor Tyrosine Kinase Like Orphan Receptor 2	Protein Coding	4
45	ROR1	Receptor Tyrosine Kinase Like Orphan Receptor 1	Protein Coding	4
46	MYC	MYC Proto-Oncogene, BHLH Transcription Factor	Protein Coding	4
47	JUN	Jun Proto-Oncogene, AP-1 Transcription Factor Subunit	Protein Coding	4
48	CTBP2	C-Terminal Binding Protein 2	Protein Coding	4
49	CTBP1	C-Terminal Binding Protein 1	Protein Coding	4
50	CSNK1A1	Casein Kinase 1 Alpha 1	Protein Coding	4
51	NKD2	NKD Inhibitor Of Wnt Signaling Pathway 2	Protein Coding	4
52	NKD1	NKD Inhibitor Of Wnt Signaling Pathway 1	Protein Coding	4
53	FOSL1	FOS Like 1, AP-1 Transcription Factor Subunit	Protein Coding	4
54	WNT16	Wnt Family Member 16	Protein Coding	4
55	FRAT1	FRAT Regulator Of Wnt Signaling Pathway 1	Protein Coding	4
56	MAP3K7	Mitogen-Activated Protein Kinase Kinase Kinase 7	Protein Coding	4
57	KREMEN1	Kringle Containing Transmembrane Protein 1	Protein Coding	3
58	PORCN	Porcupine O-Acyltransferase	Protein Coding	3
59	SOX17	SRY-Box Transcription Factor 17	Protein Coding	3
60	SFRP5	Secreted Frizzled Related Protein 5	Protein Coding	3
61	SFRP4	Secreted Frizzled Related Protein 4	Protein Coding	3
62	SFRP2	Secreted Frizzled Related Protein 2	Protein Coding	3
63	SFRP1	Secreted Frizzled Related Protein 1	Protein Coding	3
64	SENP2	SUMO Specific Peptidase 2	Protein Coding	3
65	CHD8	Chromodomain Helicase DNA Binding Protein 8	Protein Coding	3
66	SERPINF1	Serpin Family F Member 1	Protein Coding	3
67	SOST	Sclerostin	Protein Coding	3
68	DKK1	Dickkopf Wnt Signaling Pathway Inhibitor 1	Protein Coding	3
69	NOTUM	Notum, Palmitoleoyl-Protein Carboxylesterase	Protein Coding	3
70	CSNK2B	Casein Kinase 2 Beta	Protein Coding	3
71	CSNK2A2	Casein Kinase 2 Alpha 2	Protein Coding	3
72	CSNK2A1	Casein Kinase 2 Alpha 1	Protein Coding	3
73	WIF1	Wnt Inhibitory Factor 1	Protein Coding	3
74	CER1	Cerberus 1, DAN Family BMP Antagonist	Protein Coding	3
75	CSNK1A1L	Casein Kinase 1 Alpha 1 Like	Protein Coding	3
76	CXXC4	CXXC Finger Protein 4	Protein Coding	3
77	CTNNBIP1	Catenin Beta Interacting Protein 1	Protein Coding	3
78	CSNK2A3	Casein Kinase 2 Alpha 3	Protein Coding	3
79	DKK2	Dickkopf Wnt Signaling Pathway Inhibitor 2	Protein Coding	3
80	DKK4	Dickkopf Wnt Signaling Pathway Inhibitor 4	Protein Coding	3
81	FRAT2	FRAT Regulator Of Wnt Signaling Pathway 2	Protein Coding	3
82	AXIN2	Axin 2	Protein Coding	3
83	PRKCA	Protein Kinase C Alpha	Protein Coding	3
84	PRKCB	Protein Kinase C Beta	Protein Coding	3
85	PRKCG	Protein Kinase C Gamma	Protein Coding	3
86	MAPK9	Mitogen-Activated Protein Kinase 9	Protein Coding	3
87	RHOA	Ras Homolog Family Member A	Protein Coding	3
88	EZH2	Enhancer Of Zeste 2 Polycomb Repressive Complex 2 Subunit	Protein Coding	2
89	FZD4	Frizzled Class Receptor 4	Protein Coding	2
90	WNT9B	Wnt Family Member 9B	Protein Coding	2
91	PLCB2	Phospholipase C Beta 2	Protein Coding	2
92	PLCB3	Phospholipase C Beta 3	Protein Coding	2
93	PLCB4	Phospholipase C Beta 4	Protein Coding	2
94	PRKCE	Protein Kinase C Epsilon	Protein Coding	2
95	PRKCD	Protein Kinase C Delta	Protein Coding	2
96	PRKCI	Protein Kinase C Iota	Protein Coding	2
97	PRKD1	Protein Kinase D1	Protein Coding	2
98	PRKCQ	Protein Kinase C Theta	Protein Coding	2
99	PRKCZ	Protein Kinase C Zeta	Protein Coding	2
100	CAMK2B	Calcium/Calmodulin Dependent Protein Kinase II Beta	Protein Coding	2
101	CAMK2A	Calcium/Calmodulin Dependent Protein Kinase II Alpha	Protein Coding	2
102	CAMK2G	Calcium/Calmodulin Dependent Protein Kinase II Gamma	Protein Coding	2
103	CAMK2D	Calcium/Calmodulin Dependent Protein Kinase II Delta	Protein Coding	2
104	PPP3CA	Protein Phosphatase 3 Catalytic Subunit Alpha	Protein Coding	2
105	PPP3R1	Protein Phosphatase 3 Regulatory Subunit B, Alpha	Protein Coding	2
106	NFATC1	Nuclear Factor Of Activated T Cells 1	Protein Coding	2
107	NFATC2	Nuclear Factor Of Activated T Cells 2	Protein Coding	2
108	NFATC3	Nuclear Factor Of Activated T Cells 3	Protein Coding	2
109	NFATC4	Nuclear Factor Of Activated T Cells 4	Protein Coding	2
110	MAPK8	Mitogen-Activated Protein Kinase 8	Protein Coding	2
111	MAPK10	Mitogen-Activated Protein Kinase 10	Protein Coding	2
112	ROCK2	Rho Associated Coiled-Coil Containing Protein Kinase 2	Protein Coding	2
113	RAC1	Rac Family Small GTPase 1	Protein Coding	2
114	DAAM1	Dishevelled Associated Activator Of Morphogenesis 1	Protein Coding	2
115	KLF4	KLF Transcription Factor 4	Protein Coding	1
116	MTDH	Metadherin	Protein Coding	1
117	MIR452	MicroRNA 452	RNA Gene	1
118	MIR320A	MicroRNA 320a	RNA Gene	1
119	MIR18A	MicroRNA 18a	RNA Gene	1
120	ELAVL1	ELAV Like RNA Binding Protein 1	Protein Coding	1
121	SOX7	SRY-Box Transcription Factor 7	Protein Coding	1
122	WNT8A	Wnt Family Member 8A	Protein Coding	1
123	WNT8B	Wnt Family Member 8B	Protein Coding	1
124	WNT9A	Wnt Family Member 9A	Protein Coding	1
125	RSPO1	R-Spondin 1	Protein Coding	1
126	RSPO2	R-Spondin 2	Protein Coding	1
127	RSPO3	R-Spondin 3	Protein Coding	1
128	RSPO4	R-Spondin 4	Protein Coding	1
129	GSK3A	Glycogen Synthase Kinase 3 Alpha	Protein Coding	1
130	CSNK1G1	Casein Kinase 1 Gamma 1	Protein Coding	1
131	CSNK1D	Casein Kinase 1 Delta	Protein Coding	1
132	TLE1	TLE Family Member 1, Transcriptional Corepressor	Protein Coding	1
133	TLE2	TLE Family Member 2, Transcriptional Corepressor	Protein Coding	1
134	TLE3	TLE Family Member 3, Transcriptional Corepressor	Protein Coding	1
135	TLE4	TLE Family Member 4, Transcriptional Corepressor	Protein Coding	1
136	TLE5	TLE Family Member 5, Transcriptional Modulator	Protein Coding	1
137	TLE6	TLE Family Member 6, Subcortical Maternal Complex Member	Protein Coding	1
138	BTRC	Beta-Transducin Repeat Containing E3 Ubiquitin Protein Ligase	Protein Coding	1
139	SDC1	Syndecan 1	Protein Coding	1
140	SDC2	Syndecan 2	Protein Coding	1
141	SDC3	Syndecan 3	Protein Coding	1
142	SDC4	Syndecan 4	Protein Coding	1
143	GPC1	Glypican 1	Protein Coding	1
144	GPC2	Glypican 2	Protein Coding	1
145	GPC3	Glypican 3	Protein Coding	1
146	GPC5	Glypican 5	Protein Coding	1
147	GPC6	Glypican 6	Protein Coding	1
148	LGR4	Leucine Rich Repeat Containing G Protein-Coupled Receptor 4	Protein Coding	1
149	LGR5	Leucine Rich Repeat Containing G Protein-Coupled Receptor 5	Protein Coding	1
150	LGR6	Leucine Rich Repeat Containing G Protein-Coupled Receptor 6	Protein Coding	1
151	PYGO1	Pygopus Family PHD Finger 1	Protein Coding	1
152	PYGO2	Pygopus Family PHD Finger 2	Protein Coding	1
153	BCL9	BCL9 Transcription Coactivator	Protein Coding	1
154	BCL9L	BCL9 Like	Protein Coding	1
155	PLCB1	Phospholipase C Beta 1	Protein Coding	1
156	ROCK1	Rho Associated Coiled-Coil Containing Protein Kinase 1	Protein Coding	1
157	RAC2	Rac Family Small GTPase 2	Protein Coding	1
158	RAC3	Rac Family Small GTPase 3	Protein Coding	1
159	RHOB	Ras Homolog Family Member B	Protein Coding	1
160	RHOC	Ras Homolog Family Member C	Protein Coding	1
161	SRC	SRC Proto-Oncogene, Non-Receptor Tyrosine Kinase	Protein Coding	1
162	VANGL1	VANGL Planar Cell Polarity Protein 1	Protein Coding	1
163	VANGL2	VANGL Planar Cell Polarity Protein 2	Protein Coding	1
164	PPP3CC	Protein Phosphatase 3 Catalytic Subunit Gamma	Protein Coding	1
165	PPP3CB	Protein Phosphatase 3 Catalytic Subunit Beta	Protein Coding	1
166	INVS	Inversin	Protein Coding	1
167	DAAM2	Dishevelled Associated Activator Of Morphogenesis 2	Protein Coding	1
168	GPC4	Glypican 4	Protein Coding	1
169	PRICKLE2	Prickle Planar Cell Polarity Protein 2	Protein Coding	1
170	PRICKLE1	Prickle Planar Cell Polarity Protein 1	Protein Coding	1
171	LOC105372522	Uncharacterized LOC105372522	RNA Gene	1
172	PPP3R2	Protein Phosphatase 3 Regulatory Subunit B, Beta	Protein Coding	1
173	CTNND1	Catenin Delta 1	Protein Coding	1
174	CD44	CD44 Molecule (IN Blood Group)	Protein Coding	1
175	NANOG	Nanog Homeobox	Protein Coding	1
176	TP53	Tumor Protein P53	Protein Coding	1
177	SOX2	SRY-Box Transcription Factor 2	Protein Coding	1
178	PRKCH	Protein Kinase C Eta	Protein Coding	1
179	PPP2R5E	Protein Phosphatase 2 Regulatory Subunit B''Epsilon	Protein Coding	1
180	PPP2R5C	Protein Phosphatase 2 Regulatory Subunit B''Gamma	Protein Coding	1
181	PTPA	Protein Phosphatase 2 Phosphatase Activator	Protein Coding	1
182	PPP2R3A	Protein Phosphatase 2 Regulatory Subunit B''''Alpha	Protein Coding	1
183	PPP2R2C	Protein Phosphatase 2 Regulatory Subunit Bgamma	Protein Coding	1
184	PPP2R2B	Protein Phosphatase 2 Regulatory Subunit Bbeta	Protein Coding	1
185	PPP2R2A	Protein Phosphatase 2 Regulatory Subunit Balpha	Protein Coding	1
186	PPP2R1B	Protein Phosphatase 2 Scaffold Subunit Abeta	Protein Coding	1
187	PPP2R1A	Protein Phosphatase 2 Scaffold Subunit Aalpha	Protein Coding	1
188	PPP2CA	Protein Phosphatase 2 Catalytic Subunit Alpha	Protein Coding	1
189	PPARD	Peroxisome Proliferator Activated Receptor Delta	Protein Coding	1
190	POU5F1	POU Class 5 Homeobox 1	Protein Coding	1
191	PAFAH1B1	Platelet Activating Factor Acetylhydrolase 1b Regulatory Subunit 1	Protein Coding	1
192	NFYA	Nuclear Transcription Factor Y Subunit Alpha	Protein Coding	1
193	MMP7	Matrix Metallopeptidase 7	Protein Coding	1
194	LDLR	Low Density Lipoprotein Receptor	Protein Coding	1
195	RACGAP1	Rac GTPase Activating Protein 1	Protein Coding	1
196	FOXD3	Forkhead Box D3	Protein Coding	1
197	ESRRB	Estrogen Related Receptor Beta	Protein Coding	1
198	EP300	EP300 Lysine Acetyltransferase	Protein Coding	1
199	CREBBP	CREB Binding Lysine Acetyltransferase	Protein Coding	1
200	LRRK2	Leucine Rich Repeat Kinase 2	Protein Coding	1
201	MAP2K4	Mitogen-Activated Protein Kinase Kinase 4	Protein Coding	1
202	PPP2CB	Protein Phosphatase 2 Catalytic Subunit Beta	Protein Coding	1
203	PPM1J	Protein Phosphatase, Mg2+/Mn2+ Dependent 1J	Protein Coding	1
204	PPP2R3B	Protein Phosphatase 2 Regulatory Subunit B''''Beta~Name Same As:- HGNC:9310	Protein Coding	1
205	FBXW2	F-Box And WD Repeat Domain Containing 2	Protein Coding	1
206	ZBTB33	Zinc Finger And BTB Domain Containing 33	Protein Coding	1
207	TFAP2A	Transcription Factor AP-2 Alpha	Protein Coding	1
208	TCF3	Transcription Factor 3	Protein Coding	1
209	ATF3	Activating Transcription Factor 3	Protein Coding	1
210	MIR16-1	MicroRNA 16-1	RNA Gene	1
211	HNRNPU	Heterogeneous Nuclear Ribonucleoprotein U	Protein Coding	1
212	HNRNPK	Heterogeneous Nuclear Ribonucleoprotein K	Protein Coding	1
213	H19	H19 Imprinted Maternally Expressed Transcript	RNA Gene	1
214	APC2	APC Regulator Of Wnt Signaling Pathway 2	Protein Coding	1
215	CDK6	Cyclin Dependent Kinase 6	Protein Coding	1
216	RUVBL1	RuvB Like AAA ATPase 1	Protein Coding	1
217	MIR34AHG	MIR34A Host Gene	RNA Gene	1
218	CDK8	Cyclin Dependent Kinase 8	Protein Coding	1
219	MACROH2A2	MacroH2A.2 Histone	Protein Coding	1
220	MIR16-2	MicroRNA 16-2	RNA Gene	1

Disorders associated with ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Robinow syndrome, autosomal recessive 1	Enrichment	DVL1, DVL3, FZD2, ROR2, WNT5A	10.79
2	Autosomal recessive robinow syndrome	Enrichment	DVL1, DVL3, FZD2, ROR2, WNT5A	10.17
3	Robinow syndrome, autosomal dominant 1	Enrichment	DVL1, DVL3, FZD2, WNT5A	8.78
4	Autosomal dominant robinow syndrome	Enrichment	DVL1, DVL3, FZD2, WNT5A	8.78
5	Osteoporosis, juvenile	Enrichment	DKK1, WNT1, WNT3A	6.58
6	Robinow syndrome, autosomal dominant 2	Enrichment	DVL1, DVL3, FZD2	5.58
7	Colorectal cancer	Enrichment	APC, AXIN2, CCND1, CTNNB1, EP300, FZD3, TP53	5.43
8	Exudative vitreoretinopathy 1	Enrichment	CTNNB1, FZD4, LRP5	5.40
9	Polycystic liver disease	Enrichment	CTNNB1, LRP5, LRP6, RUVBL1	5.26
10	Autosomal dominant polycystic liver disease	Enrichment	CTNNB1, LRP5, LRP6, RUVBL1	5.26
11	Tooth agenesis	Enrichment	AXIN2, LRP6, WNT10A, WNT10B	4.79
12	Hepatocellular carcinoma	Enrichment	APC, AXIN1, CTNNB1, TP53	4.72
13	Exudative vitreoretinopathy	Enrichment	CTNNB1, FZD4, LRP5	4.66
14	Adult hepatocellular carcinoma	Enrichment	AXIN1, CTNNB1, TP53	4.49
15	Van buchem disease	Enrichment	LRP5, SOST	4.38
16	Robinow syndrome, autosomal dominant 3	Enrichment	DVL3, FZD2	4.38
17	Autosomal dominant non-syndromic intellectual disability	Enrichment	CAMK2A, CAMK2B, CSNK2B, PPP3CA, PRICKLE2	4.22
18	Desmoid disease, hereditary	Enrichment	APC, CTNNB1	3.91
19	Desmoid tumor	Enrichment	APC, CTNNB1	3.91
20	Osteoporosis	Enrichment	LRP5, SRC, WNT1	3.71
21	Craniopharyngioma	Enrichment	APC, CTNNB1	3.61
22	Retinopathy of prematurity	Enrichment	FZD4, LRP5	3.49
23	Brittle bone disorder	Enrichment	LRP5, SERPINF1, WNT1	3.37
24	Hepatoblastoma	Enrichment	APC, CTNNB1, TP53	3.32
25	Rubinstein-taybi syndrome 1	Enrichment	CREBBP, EP300	3.09
26	Chromosome 16p13.3 deletion syndrome, proximal	Enrichment	CREBBP, EP300	3.09
27	Adrenocortical carcinoma	Enrichment	CTNNB1, TP53	3.09
28	Gallbladder cancer	Enrichment	CTNNB1, TP53	2.95
29	Isolated split hand-split foot malformation	Enrichment	BTRC, WNT10B	2.72
30	Cat eye syndrome	Enrichment	FZD5, TFAP2A	2.66
31	Leukemia, chronic lymphocytic	Enrichment	CCND1, TP53	2.62
32	Osteogenesis imperfecta, type iv	Enrichment	SERPINF1, WNT1	2.51
33	Medulloblastoma	Enrichment	APC, CTNNB1	2.44
34	Osteogenesis imperfecta, type iii	Enrichment	SERPINF1, WNT1	2.38
35	Neural tube defects	Enrichment	VANGL1, VANGL2	2.29
36	Rare genetic intellectual disability	Enrichment	CREBBP, EP300	2.27
37	Brachydactyly, type b1	Enrichment	ROR2	2.19
38	Chiari malformation type i	Enrichment	DKK1	2.19
39	Endosteal hyperostosis, autosomal dominant	Enrichment	LRP5	2.19
40	Craniodiaphyseal dysplasia, autosomal dominant	Enrichment	SOST	2.19
41	Nail disorder, nonsyndromic congenital, 1	Enrichment	FZD6	2.19
42	Mullerian aplasia and hyperandrogenism	Enrichment	WNT4	2.19
43	Bone mineral density quantitative trait locus 1	Enrichment	LRP5	2.19
44	Exudative vitreoretinopathy 4	Enrichment	LRP5	2.19
45	Sclerosteosis 1	Enrichment	SOST	2.19
46	Focal dermal hypoplasia	Enrichment	PORCN	2.19
47	46,xx sex reversal with dysgenesis of kidneys, adrenals, and lungs	Enrichment	WNT4	2.19
48	Omodysplasia 2	Enrichment	FZD2	2.19
49	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3	Enrichment	CCND2	2.19
50	Split-hand/foot malformation 6	Enrichment	WNT10B	2.19
51	Tooth agenesis, selective, 7	Enrichment	LRP6	2.19
52	Caudal duplication anomaly	Enrichment	AXIN1	2.19
53	Tooth agenesis, selective, 8	Enrichment	WNT10B	2.19
54	Vesicoureteral reflux 3	Enrichment	SOX17	2.19
55	Ectodermal dysplasia 13, hair/tooth type	Enrichment	KREMEN1	2.19
56	Ectodermal dysplasia 17 with or without limb malformations	Enrichment	LEF1	2.19
57	Exudative vitreoretinopathy 8	Enrichment	LRP6	2.19
58	Pyle disease	Enrichment	SFRP4	2.19
59	Deafness, autosomal recessive 108	Enrichment	ROR1	2.19
60	Diarrhea 9	Enrichment	WNT2B	2.19
61	Osteoporosis-pseudoglioma syndrome	Enrichment	LRP5	2.19
62	Coronary artery disease, autosomal dominant 2	Enrichment	LRP6	2.19
63	Bone mineral density quantitative trait locus 16	Enrichment	WNT1	2.19
64	Polycystic liver disease 4 with or without kidney cysts	Enrichment	LRP5	2.19
65	Santos syndrome	Enrichment	WNT7A	2.19
66	Microphthalmia/coloboma 11	Enrichment	FZD5	2.19
67	Okur-chung neurodevelopmental syndrome	Enrichment	CSNK2A1	2.19
68	Craniometadiaphyseal osteosclerosis with hip dysplasia	Enrichment	AXIN1	2.19
69	Adenoid ameloblastoma	Enrichment	CTNNB1	2.19
70	Craniodigital syndrome and intellectual disability syndrome	Enrichment	CSNK2B	2.19
71	Lrp5-related primary osteoporosis	Enrichment	LRP5	2.19
72	Pulmonary hypertension, primary, 7	Enrichment	SOX17	2.19
73	Familial adenomatous polyposis	Enrichment	APC	2.19
74	Gardner syndrome	Enrichment	APC	2.19
75	Osteosclerosis-developmental delay-craniosynostosis syndrome	Enrichment	LRP5	2.19
76	5q22 microdeletion syndrome	Enrichment	APC	2.19
77	Attenuated familial adenomatous polyposis	Enrichment	APC	2.19
78	Microcystic stromal tumor	Enrichment	CTNNB1	2.19
79	Ovarian cancer	Enrichment	APC, AXIN2, CTNNB1, TP53	2.17
80	Cardiospondylocarpofacial syndrome	Enrichment	MAP3K7	2.15
81	Oligodontia-colorectal cancer syndrome	Enrichment	AXIN2	2.15
82	Microcephaly 12, primary, autosomal recessive	Enrichment	CDK6	2.15
83	Frontometaphyseal dysplasia 2	Enrichment	MAP3K7	2.15
84	Agammaglobulinemia 8b, autosomal recessive	Enrichment	TCF3	2.15
85	Cortical dysplasia, complex, with other brain malformations 10	Enrichment	APC2	2.15
86	Developmental and epileptic encephalopathy 54	Enrichment	HNRNPU	2.15
87	Intellectual developmental disorder, autosomal recessive 74	Enrichment	APC2	2.15
88	Agammaglobulinemia 8a, autosomal dominant	Enrichment	TCF3	2.15
89	Sotos syndrome 3	Enrichment	APC2	2.15
90	Beckwith-wiedemann syndrome due to 11p15 microdeletion	Enrichment	H19	2.15
91	1q44 microdeletion syndrome	Enrichment	HNRNPU	2.15
92	Macs syndrome	Enrichment	PORCN, WNT7B	2.14
93	Spinocerebellar ataxia 12	Enrichment	PPP2R2B	2.13
94	Autoimmune lymphoproliferative syndrome, type iii	Enrichment	PRKCD	2.13
95	Parkinson disease 25, autosomal recessive early-onset, with impaired intellectual development	Enrichment	PTPA	2.13
96	Bone marrow failure syndrome 5	Enrichment	TP53	2.13
97	Houge-janssens syndrome 4	Enrichment	PPP2R5C	2.13
98	Papilloma of choroid plexus	Enrichment	TP53	2.13
99	Basal cell carcinoma 7	Enrichment	TP53	2.13
100	Anaplastic thyroid carcinoma	Enrichment	TP53	2.13
101	Houge-janssens syndrome 2	Enrichment	PPP2R1A	2.13
102	Spinocerebellar ataxia 14	Enrichment	PRKCG	2.13
103	Deafness, autosomal recessive 35	Enrichment	ESRRB	2.13
104	Ductal carcinoma in situ	Enrichment	TP53	2.13
105	Congenital heart defects and ectodermal dysplasia	Enrichment	PRKD1	2.13
106	Ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies	Enrichment	RHOA	2.13
107	Menke-hennekam syndrome 1	Enrichment	CREBBP	2.13
108	Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies	Enrichment	RHOA	2.13
109	Thyroid gland undifferentiated carcinoma	Enrichment	TP53	2.13
110	Small-cell carcinoma of the ovary of hypercalcemic type	Enrichment	TP53	2.13
111	Rubinstein-taybi syndrome due to 16p13.3 microdeletion	Enrichment	CREBBP	2.13
112	Diffuse pediatric-type high-grade glioma, h3-wildtype and idh-wildtype	Enrichment	TP53	2.13
113	Congenital dyserythropoietic anemia type iiib	Enrichment	RACGAP1	2.13
114	Choroid plexus cancer	Enrichment	TP53	2.13
115	Menke-hennekam syndrome	Enrichment	CREBBP	2.13
116	Pleomorphic xanthoastrocytoma	Enrichment	TP53	2.13
117	Anemia, congenital dyserythropoietic, type iiib, autosomal recessive	Enrichment	RACGAP1	2.13
118	Lissencephaly due to lis1 mutation	Enrichment	PAFAH1B1	2.13
119	Ppp2r1a-related neurodevelopmental disorder	Enrichment	PPP2R1A	2.13
120	Malignant epithelial tumor of salivary glands	Enrichment	PRKD1	2.13
121	Myeloma, multiple	Enrichment	CCND1, CREBBP, TP53	2.08
122	Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis	Enrichment	RAC2	2.08
123	Advanced sleep phase syndrome, familial, 2	Enrichment	CSNK1D	2.08
124	Bone mineral density quantitative trait locus 17	Enrichment	LGR4	2.08
125	Spondylometaphyseal dysplasia with corneal dystrophy	Enrichment	PLCB3	2.08
126	Intellectual developmental disorder, autosomal recessive 63	Enrichment	CAMK2A	2.08
127	Developmental and epileptic encephalopathy 91	Enrichment	PPP3CA	2.08
128	Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies	Enrichment	RAC3	2.08
129	Intellectual developmental disorder, autosomal dominant 54	Enrichment	CAMK2B	2.08
130	Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development	Enrichment	PPP3CA	2.08
131	Humerofemoral hypoplasia with radiotibial ray deficiency	Enrichment	RSPO2	2.08
132	Auriculocondylar syndrome 2a	Enrichment	PLCB4	2.08
133	Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia	Enrichment	RAC2	2.08
134	Palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,xx sex reversal	Enrichment	RSPO1	2.08
135	Oocyte/zygote/embryo maturation arrest 15	Enrichment	TLE6	2.08
136	Thrombocytopenia 6	Enrichment	SRC	2.08
137	Tetraamelia syndrome 2	Enrichment	RSPO2	2.08
138	Intellectual developmental disorder, autosomal dominant 53	Enrichment	CAMK2A	2.08
139	Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia	Enrichment	RAC2	2.08
140	Auriculocondylar syndrome 2b	Enrichment	PLCB4	2.08
141	Intellectual developmental disorder, autosomal dominant 59	Enrichment	CAMK2G	2.08
142	Palmoplantar keratoderma-xx sex reversal-predisposition to squamous cell carcinoma syndrome	Enrichment	RSPO1	2.08
143	Infantile lad-like disease due to rac2 deficiency	Enrichment	RAC2	2.08
144	Reticular dysgenesis-like severe combined immunodeficiency	Enrichment	RAC2	2.08
145	Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom	Enrichment	RAC1	2.08
146	Rac2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome	Enrichment	RAC2	2.08
147	Keipert syndrome	Enrichment	GPC4	2.08
148	Diffuse large b-cell lymphoma	Enrichment	CREBBP, TP53	2.06
149	Microphthalmia	Enrichment	TFAP2A, WNT7B	1.97
150	Ectrodactyly and ectodermal dysplasia without cleft lip/palate	Enrichment	LEF1	1.89
151	Burkitt lymphoma	Enrichment	MYC	1.89
152	Tooth agenesis, selective, 4	Enrichment	WNT10A	1.89
153	Craniodiaphyseal dysplasia	Enrichment	SOST	1.89
154	Schopf-schulz-passarge syndrome	Enrichment	WNT10A	1.89
155	Ulna and fibula, absence of, with severe limb deficiency	Enrichment	WNT7A	1.89
156	Bladder exstrophy and epispadias complex	Enrichment	WNT3	1.89
157	Osteopathia striata with cranial sclerosis	Enrichment	CTNNB1	1.89
158	Quebec platelet disorder	Enrichment	PLAU	1.89
159	Odontoonychodermal dysplasia	Enrichment	WNT10A	1.89
160	Tetraamelia syndrome 1	Enrichment	WNT3	1.89
161	Osteogenesis imperfecta, type xv	Enrichment	WNT1	1.89
162	Fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly	Enrichment	WNT7A	1.89
163	Hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome	Enrichment	CTBP1	1.89
164	Poirier-bienvenu neurodevelopmental syndrome	Enrichment	CSNK2B	1.89
165	Sclerosteosis	Enrichment	SOST	1.89
166	Childhood hepatocellular carcinoma	Enrichment	CTNNB1	1.89
167	Split hand-foot malformation	Enrichment	LEF1	1.89
168	Periampullary adenoma	Enrichment	APC	1.89
169	Gastric adenocarcinoma and proximal polyposis of the stomach	Enrichment	APC	1.89
170	14q11.2 microduplication syndrome	Enrichment	CHD8	1.89
171	Juvenile nasopharyngeal angiofibroma	Enrichment	CTNNB1	1.89
172	Teratoma	Enrichment	CTNNB1	1.89
173	Osteosclerosis	Enrichment	LRP5	1.89
174	Bladder exstrophy-epispadias-cloacal exstrophy complex	Enrichment	WNT3	1.89
175	Ebstein anomaly	Enrichment	CDK8	1.85
176	Immunodeficiency, common variable, 15	Enrichment	RUVBL1	1.85
177	Esotropia	Enrichment	TFAP2A	1.85
178	Intellectual developmental disorder with hypotonia and behavioral abnormalities	Enrichment	CDK8	1.85
179	B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)	Enrichment	TCF3	1.85
180	B-lymphoblastic leukemia/lymphoma with t(17;19)	Enrichment	TCF3	1.85
181	Lens subluxation	Enrichment	TFAP2A	1.85
182	Silver-russell syndrome due to an imprinting defect of 11p15	Enrichment	H19	1.85
183	Silver-russell syndrome due to 11p15 microduplication	Enrichment	H19	1.85
184	Blepharocheilodontic syndrome 1	Enrichment	CTNND1	1.83
185	Anemia, congenital dyserythropoietic, type iiia	Enrichment	RACGAP1	1.83
186	Adrenocortical carcinoma, hereditary	Enrichment	TP53	1.83
187	Thumb deformity	Enrichment	CREBBP	1.83
188	Cervical cancer	Enrichment	TP53	1.83
189	Parkinson disease 8, autosomal dominant	Enrichment	LRRK2	1.83
190	Lissencephaly 1	Enrichment	PAFAH1B1	1.83
191	Lymphoma, hodgkin, classic	Enrichment	TP53	1.83
192	Blepharocheilodontic syndrome 2	Enrichment	CTNND1	1.83
193	Menke-hennekam syndrome 2	Enrichment	EP300	1.83
194	Hyperlipoproteinemia, type iii	Enrichment	LDLR	1.83
195	Acute myeloid leukemia with kat6a-crebbp fusion	Enrichment	CREBBP	1.83
196	Congenital fibrosarcoma	Enrichment	TP53	1.83
197	Li-fraumeni syndrome 1	Enrichment	TP53	1.83
198	Sarcoma	Enrichment	TP53	1.83
199	Cervix carcinoma	Enrichment	TP53	1.83
200	Hodgkin's lymphoma	Enrichment	TP53	1.83
201	Houge-janssens syndrome 3	Enrichment	PPP2CA	1.83
202	Pleomorphic rhabdomyosarcoma	Enrichment	TP53	1.83
203	Omodysplasia 1	Enrichment	GPC6	1.78
204	Intellectual developmental disorder, autosomal dominant 48	Enrichment	RAC1	1.78
205	Delayed puberty, self-limited	Enrichment	LGR4	1.78
206	Ocular melanoma	Enrichment	PLCB4	1.78
207	Joint contractures, osteochondromas, and b-cell lymphoma	Enrichment	NFATC2	1.78
208	Isolated anencephaly	Enrichment	VANGL2	1.78
209	Isolated exencephaly	Enrichment	VANGL2	1.78
210	Breast cancer	Enrichment	APC, JUN, TP53	1.74
211	Prognathism, mandibular	Enrichment	CSNK2B	1.71
212	Mullerian duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies	Enrichment	WNT4	1.71
213	Microphthalmia, syndromic 9	Enrichment	WNT7B	1.71
214	Weaver syndrome	Enrichment	EZH2	1.71
215	Tooth agenesis, selective, 2	Enrichment	WNT10A	1.71
216	Osteopetrosis, autosomal dominant 1	Enrichment	LRP5	1.71
217	Neurodevelopmental disorder with spastic diplegia and visual defects	Enrichment	CTNNB1	1.71
218	Cenani-lenz syndactyly syndrome	Enrichment	APC	1.71
219	Osteogenesis imperfecta, type vi	Enrichment	SERPINF1	1.71
220	Anus, imperforate	Enrichment	CTNNB1	1.71
221	Exudative vitreoretinopathy 7	Enrichment	CTNNB1	1.71
222	High-grade b-cell lymphoma double-hit/triple-hit	Enrichment	MYC	1.71
223	Nail disease	Enrichment	FZD6	1.71
224	Familial vesicoureteral reflux	Enrichment	SOX17	1.71
225	Tetraamelia syndrome	Enrichment	WNT3	1.71
226	Colon adenocarcinoma	Enrichment	APC	1.71
227	Apc-associated polyposis conditions	Enrichment	APC	1.71
228	Bladder cancer	Enrichment	CTNNB1, TP53	1.71
229	Neurodevelopmental disorder with progressive spasticity and brain abnormalities	Enrichment	RUVBL1	1.67
230	Frontometaphyseal dysplasia	Enrichment	MAP3K7	1.67
231	Beckwith-wiedemann syndrome due to imprinting defect of 11p15	Enrichment	H19	1.67
232	Hypercholesterolemia, familial, 2	Enrichment	LDLR	1.65
233	Klippel-feil syndrome 1, autosomal dominant	Enrichment	LRRK2	1.65
234	Intellectual developmental disorder with microcephaly and pontine and cerebellar hypoplasia	Enrichment	LDLR	1.65
235	Band heterotopia	Enrichment	PAFAH1B1	1.65
236	Autoimmune disease 1	Enrichment	FOXD3	1.65
237	Osteogenic sarcoma	Enrichment	TP53	1.65
238	Hypercholesterolemia, familial, 4	Enrichment	LDLR	1.65
239	Nasopharyngeal carcinoma	Enrichment	TP53	1.65
240	Miller-dieker lissencephaly syndrome	Enrichment	PAFAH1B1	1.65
241	Chromosome 17p13.3, centromeric, duplication syndrome	Enrichment	PAFAH1B1	1.65
242	Tethered spinal cord syndrome	Enrichment	CREBBP	1.65
243	Syndromic x-linked intellectual disability najm type	Enrichment	LDLR	1.65
244	Atypical teratoid rhabdoid tumor	Enrichment	TP53	1.65
245	Anaplastic astrocytoma	Enrichment	TP53	1.65
246	Squamous cell carcinoma	Enrichment	TP53	1.65
247	Adenocarcinoma	Enrichment	TP53	1.65
248	Intraocular pressure quantitative trait locus	Enrichment	CREBBP	1.65
249	Bone osteosarcoma	Enrichment	TP53	1.65
250	Autism	Enrichment	CAMK2G, CHD8, TCF7L2	1.64
251	Nail disorder, nonsyndromic congenital, 4	Enrichment	RSPO4	1.60
252	Simpson-golabi-behmel syndrome, type 1	Enrichment	GPC3	1.60
253	Advanced sleep phase syndrome	Enrichment	CSNK1D	1.60
254	Nephronophthisis 2	Enrichment	INVS	1.60
255	Epilepsy, progressive myoclonic, 1b	Enrichment	PRICKLE1	1.60
256	Nephrotic syndrome, type 24	Enrichment	DAAM2	1.60
257	Acyl-coa dehydrogenase, very long-chain, deficiency of	Enrichment	DVL2	1.59
258	Ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive	Enrichment	WNT10A	1.59
259	Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1	Enrichment	CCND2	1.59
260	Pilomatrixoma	Enrichment	CTNNB1	1.59
261	Alazami syndrome	Enrichment	CTNNB1	1.59
262	Mantle cell lymphoma	Enrichment	CCND1	1.59
263	Enophthalmos	Enrichment	CSNK2B	1.59
264	Syndactyly	Enrichment	CSNK2B	1.59
265	Intellectual developmental disorder with autism and macrocephaly	Enrichment	CHD8	1.59
266	Orofacial cleft	Enrichment	LRP6	1.59
267	Ectodermal dysplasia	Enrichment	WNT10A	1.59
268	Eyelid coloboma	Enrichment	FZD5	1.59
269	Vitreoretinopathy	Enrichment	LRP5	1.59
270	Orofacial clefting syndrome	Enrichment	LRP6	1.59
271	Lens coloboma	Enrichment	FZD5	1.59
272	Branchiooculofacial syndrome	Enrichment	TFAP2A	1.55
273	Au-kline syndrome	Enrichment	HNRNPK	1.55
274	Small cell cancer of the lung	Enrichment	TP53	1.53
275	Microphthalmia, syndromic 3	Enrichment	SOX2	1.53
276	Thyroid cancer, nonmedullary, 1	Enrichment	TP53	1.53
277	Lung sarcomatoid carcinoma	Enrichment	TP53	1.53
278	Hereditary ataxia	Enrichment	PRKCG	1.53
279	Embryonal rhabdomyosarcoma	Enrichment	TP53	1.53
280	Distal arthrogryposis	Enrichment	FZD3, ROR2	1.52
281	Alzheimer disease 2	Enrichment	PLAU	1.49
282	Von hippel-lindau syndrome	Enrichment	CCND1	1.49
283	Familial adenomatous polyposis 1	Enrichment	APC	1.49
284	Congenital ptosis	Enrichment	CHD8	1.49
285	Autosomal recessive hypohidrotic ectodermal dysplasia syndrome	Enrichment	WNT10A	1.49
286	Coloboma of choroid and retina	Enrichment	FZD5	1.49
287	Auriculocondylar syndrome 1	Enrichment	PLCB4	1.48
288	Developmental and epileptic encephalopathy 12	Enrichment	PLCB1	1.48
289	Sacral defect with anterior meningocele	Enrichment	VANGL1	1.48
290	Autism spectrum disorder	Enrichment	CHD8, CSNK2A1, CSNK2B	1.47
291	Sotos syndrome	Enrichment	APC2	1.45
292	Amblyopia	Enrichment	TFAP2A	1.45
293	Hyperlipidemia, familial combined, 3	Enrichment	LDLR	1.44
294	Norrie disease	Enrichment	FZD4	1.44
295	Rhabdomyosarcoma 2	Enrichment	TP53	1.44
296	Chromosome 15q11.2 deletion syndrome	Enrichment	PAFAH1B1	1.44
297	Rubinstein-taybi syndrome 2	Enrichment	EP300	1.44
298	Lymphoma	Enrichment	TP53	1.44
299	Persistent hyperplastic primary vitreous	Enrichment	FZD4	1.44
300	Acute megakaryocytic leukemia	Enrichment	TP53	1.44
301	Coloboma of optic nerve	Enrichment	FZD5	1.42
302	Weyers acrofacial dysostosis	Enrichment	CTNNB1	1.42
303	Wolf-hirschhorn syndrome	Enrichment	CTBP1	1.42
304	Split-hand/foot malformation 1	Enrichment	LEF1	1.42
305	Diarrhea	Enrichment	WNT2B	1.42
306	Multicystic kidney dysplasia	Enrichment	FZD3	1.42
307	Multicystic dysplastic kidney	Enrichment	FZD3	1.42
308	Gastric cancer	Enrichment	APC, TP53	1.39
309	Female infertility due to oocyte meiotic arrest	Enrichment	TLE6	1.38
310	Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis	Enrichment	PRICKLE2	1.38
311	Branchiootorenal syndrome 1	Enrichment	TFAP2A	1.38
312	Hemihyperplasia, isolated	Enrichment	H19	1.38
313	Hereditary breast carcinoma	Enrichment	APC, TP53	1.37
314	Li-fraumeni syndrome	Enrichment	TP53	1.36
315	Machado-joseph disease	Enrichment	LRRK2	1.36
316	Cowden syndrome 1	Enrichment	LDLR	1.36
317	Renal dysplasia, cystic	Enrichment	WNT9B	1.36
318	Renal hypoplasia	Enrichment	WNT9B	1.36
319	Lipid metabolism disorder	Enrichment	LDLR	1.36
320	Breast adenocarcinoma	Enrichment	TP53	1.36
321	Hypertrichosis	Enrichment	CREBBP	1.36
322	Cleft lip with or without cleft palate	Enrichment	CTNND1	1.36
323	Overgrowth syndrome	Enrichment	CHD8	1.35
324	Benign epilepsy with centrotemporal spikes	Enrichment	PRICKLE1, PRICKLE2	1.33
325	Branchiootorenal syndrome	Enrichment	TFAP2A	1.31
326	Melanoma, uveal	Enrichment	PLCB4	1.31
327	Centralopathic epilepsy	Enrichment	PRICKLE1, PRICKLE2	1.30
328	Esophageal cancer	Enrichment	TP53	1.29
329	Squamous cell carcinoma, head and neck	Enrichment	TP53	1.29
330	Coats disease	Enrichment	FZD4	1.29
331	Essential thrombocythemia	Enrichment	TP53	1.29
332	B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)	Enrichment	TP53	1.29
333	West syndrome	Enrichment	CSNK1E, PLCB1	1.28
334	Colonic benign neoplasm	Enrichment	APC	1.24
335	Myelofibrosis	Enrichment	SRC	1.24
336	Glioma susceptibility 1	Enrichment	TP53	1.24
337	Renal hypodysplasia/aplasia 1	Enrichment	WNT9B	1.24
338	Lymphoma, non-hodgkin, familial	Enrichment	TP53	1.24
339	Lennox-gastaut syndrome	Enrichment	MAPK10	1.24
340	Homozygous familial hypercholesterolemia	Enrichment	LDLR	1.24
341	Complex neurodevelopmental disorder	Enrichment	CDK8, CSNK2A1, TCF7L2	1.23
342	Tooth agenesis, selective, 1	Enrichment	AXIN2	1.20
343	Tracheoesophageal fistula with or without esophageal atresia	Enrichment	APC2	1.20
344	Charge syndrome	Enrichment	EP300	1.19
345	Inflammatory bowel disease 1	Enrichment	PRKCQ	1.19
346	Coronary heart disease 5	Enrichment	LDLR	1.19
347	Primary hyperaldosteronism	Enrichment	TP53	1.19
348	Autosomal dominant cerebellar ataxia	Enrichment	LRRK2	1.19
349	Renal agenesis, bilateral	Enrichment	WNT9B	1.19
350	Infantile nephronophthisis	Enrichment	INVS	1.19
351	Inherited cancer-predisposing syndrome	Enrichment	APC, AXIN2, EZH2	1.16
352	Heritable pulmonary arterial hypertension	Enrichment	SOX17	1.16
353	Isolated tracheo-esophageal fistula	Enrichment	APC2	1.16
354	Autosomal non-syndromic agammaglobulinemia	Enrichment	TCF3	1.16
355	Stroke, ischemic	Enrichment	PRKCH	1.14
356	Familial colorectal cancer	Enrichment	TP53	1.14
357	Developmental and epileptic encephalopathy 14	Enrichment	PLCB1	1.14
358	Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies	Enrichment	RAC1	1.14
359	Myelodysplastic syndrome	Enrichment	TP53	1.10
360	Nanophthalmos	Enrichment	SOX2	1.10
361	Microphthalmia/coloboma 12	Enrichment	FZD5	1.09
362	Pulmonary hypertension, primary, 1	Enrichment	SOX17	1.09
363	Epicanthus	Enrichment	TFAP2A	1.08
364	Septooptic dysplasia	Enrichment	SOX2	1.07
365	Early-onset parkinson's disease	Enrichment	LRRK2	1.07
366	Lip and oral cavity carcinoma	Enrichment	TP53	1.07
367	Diaphragmatic hernia, congenital	Enrichment	CDK8	1.05
368	Hypercholesterolemia, familial, 1	Enrichment	LDLR	1.03
369	Chromosome 1p36 deletion syndrome	Enrichment	PRKCZ	1.03
370	Chronic kidney disease	Enrichment	WNT9B	1.03
371	Coloboma of macula	Enrichment	FZD5	1.03
372	Hydrocephalus	Enrichment	FZD3	1.03
373	Lung cancer susceptibility 3	Enrichment	TP53	1.00
374	Heart disease	Enrichment	CREBBP	1.00
375	Wilms tumor 1	Enrichment	H19	0.99
376	Senior-loken syndrome 1	Enrichment	INVS	0.98
377	Alzheimer disease, familial, 1	Enrichment	PLAU	0.98
378	Polydactyly, postaxial, type a1	Enrichment	EP300	0.97
379	Corpus callosum, agenesis of	Enrichment	CREBBP	0.97
380	Familial hypercholesterolemia	Enrichment	LDLR	0.97
381	Isolated corpus callosum agenesis	Enrichment	CREBBP	0.97
382	Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome	Enrichment	CREBBP	0.97
383	Hydrocephalus, congenital, 1	Enrichment	CDK8	0.96
384	Myoclonic epilepsy of unverricht and lundborg	Enrichment	PRICKLE1	0.95
385	Rhabdomyosarcoma	Enrichment	TP53	0.95
386	Gliosarcoma	Enrichment	TP53	0.95
387	Giant cell glioblastoma	Enrichment	TP53	0.92
388	Heart, malformation of	Enrichment	CDK8	0.92
389	Esophageal atresia/tracheoesophageal fistula	Enrichment	APC2	0.89
390	Parkinson's disease	Enrichment	LRRK2	0.88
391	Precursor t-cell acute lymphoblastic leukemia	Enrichment	MYC	0.86
392	Lissencephaly	Enrichment	PAFAH1B1	0.84
393	Developmental and epileptic encephalopathy 1	Enrichment	CSNK1E	0.82
394	Craniosynostosis	Enrichment	GPC4	0.81
395	Hydrops fetalis, nonimmune	Enrichment	FZD6	0.81
396	Diamond-blackfan anemia 1	Enrichment	TP53	0.80
397	Cardiomyopathy, dilated, 1a	Enrichment	NFATC2	0.79
398	Parkinson disease, late-onset	Enrichment	LRRK2	0.78
399	Scoliosis	Enrichment	CREBBP	0.78
400	Pancreatic cancer	Enrichment	TP53	0.77
401	Non-immune hydrops fetalis	Enrichment	FZD6	0.74
402	Congenital nervous system abnormality	Enrichment	CREBBP, CTNNB1	0.73
403	Nervous system disease	Enrichment	CREBBP, CTNNB1	0.73
404	Hirschsprung disease 1	Enrichment	AXIN2	0.73
405	Prostate cancer	Enrichment	TP53	0.71
406	Primary autosomal recessive microcephaly	Enrichment	CDK6	0.69
407	Lung cancer	Enrichment	PPP2R1B	0.67
408	Fetal akinesia deformation sequence 1	Enrichment	ROR2	0.67
409	Microcephaly	Enrichment	CTNNB1, EP300	0.63
410	Diamond-blackfan anemia	Enrichment	TP53	0.63
411	Type 2 diabetes mellitus	Enrichment	TCF7L2	0.62
412	Nephronophthisis	Enrichment	INVS	0.61
413	Genetic steroid-resistant nephrotic syndrome	Enrichment	DAAM2	0.60
414	Dystonia	Enrichment	CAMK2B	0.59
415	Leukemia, acute myeloid	Enrichment	TP53	0.59
416	Hypertelorism	Enrichment	TFAP2A	0.51
417	Thrombocytopenia	Enrichment	SRC	0.48
418	Hereditary breast ovarian cancer syndrome	Enrichment	TP53	0.47
419	Body mass index quantitative trait locus 11	Enrichment	SDC3	0.46
420	Deafness, autosomal recessive	Enrichment	ESRRB	0.42
421	Undetermined early-onset epileptic encephalopathy	Enrichment	PPP3CA	0.42
422	Autosomal recessive nonsyndromic deafness	Enrichment	ESRRB	0.42
423	Rare autosomal recessive non-syndromic sensorineural deafness type dfnb	Enrichment	ROR1	0.36
424	Rare genetic deafness	Enrichment	ESRRB	0.35
425	Hereditary retinal dystrophy	Enrichment	FZD4, LRP5	0.19
426	Fundus dystrophy	Enrichment	FZD4, LRP5	0.19

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁸ Cell Signaling Technology

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Pathway Network for ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Pathway network for the ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

Member Pathways for ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Pathways in the ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

Gene overlap in member pathways for ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

Associated Genes for ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Associated Disorders for ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Disorders associated with ncRNAs involved in Wnt signaling in hepatocellular carcinoma SuperPath

STRING Interaction Network for ncRNAs involved in Wnt signaling in hepatocellular carcinoma

Sources for ncRNAs involved in Wnt signaling in hepatocellular carcinoma