White fat cell differentiation

No Pathway Network information available for White fat cell differentiation

Pathways in the White fat cell differentiation SuperPath

#	Name	Source	Genes
1	White fat cell differentiation	WikiPathways	CEBPA CEBPB CEBPD CREB1 CTNNA1 DDIT3 EBF1 EGR2 FOXO1 GATA2 GATA3 INS IRF3 IRF4 KLF15 KLF2 KLF4 KLF5 MECOM NR1H3 NR2F2 NR3C1 PPARG RARA RORA SREBF1 STAT5A STAT5B TCF7L1 TLE3 WNT10B ZNF423 (see all 32) (see less)
2	Transcriptional cascade regulating adipogenesis	WikiPathways	CEBPA CEBPB CEBPD CEBPG DDIT3 EGR2 KLF15 KLF2 KLF5 PPARG SREBF1 (see all 11) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	KLF5	KLF Transcription Factor 5	Protein Coding	2
2	SREBF1	Sterol Regulatory Element Binding Transcription Factor 1	Protein Coding	2
3	PPARG	Peroxisome Proliferator Activated Receptor Gamma	Protein Coding	2
4	KLF15	KLF Transcription Factor 15	Protein Coding	2
5	EGR2	Early Growth Response 2	Protein Coding	2
6	DDIT3	DNA Damage Inducible Transcript 3	Protein Coding	2
7	CEBPD	CCAAT Enhancer Binding Protein Delta	Protein Coding	2
8	CEBPB	CCAAT Enhancer Binding Protein Beta	Protein Coding	2
9	CEBPA	CCAAT Enhancer Binding Protein Alpha	Protein Coding	2
10	KLF2	KLF Transcription Factor 2	Protein Coding	2
11	KLF4	KLF Transcription Factor 4	Protein Coding	1
12	TCF7L1	Transcription Factor 7 Like 1	Protein Coding	1
13	WNT10B	Wnt Family Member 10B	Protein Coding	1
14	TLE3	TLE Family Member 3, Transcriptional Corepressor	Protein Coding	1
15	NR2F2	Nuclear Receptor Subfamily 2 Group F Member 2	Protein Coding	1
16	STAT5B	Signal Transducer And Activator Of Transcription 5B	Protein Coding	1
17	STAT5A	Signal Transducer And Activator Of Transcription 5A	Protein Coding	1
18	RORA	RAR Related Orphan Receptor A	Protein Coding	1
19	RARA	Retinoic Acid Receptor Alpha	Protein Coding	1
20	IRF4	Interferon Regulatory Factor 4	Protein Coding	1
21	IRF3	Interferon Regulatory Factor 3	Protein Coding	1
22	INS	Insulin	Protein Coding	1
23	NR3C1	Nuclear Receptor Subfamily 3 Group C Member 1	Protein Coding	1
24	GATA3	GATA Binding Protein 3	Protein Coding	1
25	GATA2	GATA Binding Protein 2~Name Same As:- HGNC:18350	Protein Coding	1
26	ZNF423	Zinc Finger Protein 423	Protein Coding	1
27	FOXO1	Forkhead Box O1	Protein Coding	1
28	MECOM	MDS1 And EVI1 Complex Locus	Protein Coding	1
29	EBF1	EBF Transcription Factor 1	Protein Coding	1
30	CTNNA1	Catenin Alpha 1	Protein Coding	1
31	CREB1	CAMP Responsive Element Binding Protein 1	Protein Coding	1
32	NR1H3	Nuclear Receptor Subfamily 1 Group H Member 3	Protein Coding	1
33	CEBPG	CCAAT Enhancer Binding Protein Gamma	Protein Coding	1

Disorders associated with White fat cell differentiation SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Acute promyelocytic leukemia	Enrichment	RARA, STAT5B	3.38
2	Charcot-marie-tooth disease, demyelinating, type 1d	Enrichment	EGR2	3.09
3	Mucoepithelial dysplasia, hereditary	Enrichment	SREBF1	3.09
4	Ifap syndrome 2	Enrichment	SREBF1	3.09
5	Pparg-associated congenital generalized lipodystrophy	Enrichment	PPARG	3.09
6	Charcot-marie-tooth disease type 1d	Enrichment	EGR2	3.09
7	Acute myeloid leukemia with mutated cebpa	Enrichment	CEBPA	3.09
8	Carotid intimal medial thickness 1	Enrichment	PPARG	2.79
9	Neuropathy, congenital hypomyelinating, 1, autosomal recessive	Enrichment	EGR2	2.79
10	Cardiomyopathy, dilated, 1ff	Enrichment	KLF5	2.79
11	Familial partial lipodystrophy	Enrichment	PPARG	2.79
12	Macular dystrophy, patterned, 2	Enrichment	CTNNA1	2.63
13	Skin/hair/eye pigmentation, variation in, 8	Enrichment	IRF4	2.63
14	Split-hand/foot malformation 6	Enrichment	WNT10B	2.63
15	Glucocorticoid resistance, generalized	Enrichment	NR3C1	2.63
16	Tooth agenesis, selective, 8	Enrichment	WNT10B	2.63
17	Encephalopathy, acute, infection-induced 7	Enrichment	IRF3	2.63
18	Growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant	Enrichment	STAT5B	2.63
19	Immunodeficiency 131	Enrichment	IRF4	2.63
20	46,xx sex reversal 5	Enrichment	NR2F2	2.63
21	Lymphedema, primary, with myelodysplasia	Enrichment	GATA2	2.63
22	Radioulnar synostosis with amegakaryocytic thrombocytopenia 2	Enrichment	MECOM	2.63
23	Immunodeficiency 21	Enrichment	GATA2	2.63
24	Nephronophthisis 14	Enrichment	ZNF423	2.63
25	Deafness-lymphedema-leukemia syndrome	Enrichment	GATA2	2.63
26	Whipple disease	Enrichment	IRF4	2.63
27	Ifap syndrome 1, with or without bresheck syndrome	Enrichment	SREBF1	2.61
28	Myxoid liposarcoma	Enrichment	DDIT3	2.61
29	Charcot-marie-tooth disease type 1	Enrichment	EGR2	2.61
30	Lipodystrophy, familial partial, type 3	Enrichment	PPARG	2.49
31	Leptin deficiency or dysfunction	Enrichment	PPARG	2.49
32	Congenital generalized lipodystrophy	Enrichment	PPARG	2.49
33	Inherited cancer-predisposing syndrome	Enrichment	CEBPA, CTNNA1, MECOM	2.44
34	Leukemia, acute myeloid	Enrichment	CEBPA, GATA2	2.40
35	Hypertrophic neuropathy of dejerine-sottas	Enrichment	EGR2	2.39
36	Inherited acute myeloid leukemia	Enrichment	CEBPA	2.39
37	Acute myeloid leukemia with t(8;21)(q22;q22) translocation	Enrichment	CEBPA	2.39
38	Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome	Enrichment	GATA3	2.33
39	Galactosemia ii	Enrichment	NR3C1	2.33
40	Growth hormone insensitivity syndrome with immune dysregulation 1, autosomal recessive	Enrichment	STAT5B	2.33
41	Histiocytoma, angiomatoid fibrous	Enrichment	CREB1	2.33
42	Maturity-onset diabetes of the young, type 10	Enrichment	INS	2.33
43	Hyperproinsulinemia	Enrichment	INS	2.33
44	Diabetes mellitus, permanent neonatal, 4	Enrichment	INS	2.33
45	B-lymphoblastic leukemia/lymphoma with hyperdiploidy	Enrichment	GATA3	2.33
46	Hypoparathyroidism-deafness-renal disease syndrome	Enrichment	GATA3	2.33
47	Intellectual developmental disorder with or without epilepsy or cerebellar ataxia	Enrichment	RORA	2.33
48	Radioulnar synostosis	Enrichment	MECOM	2.33
49	Autosomal dominant nonsyndromic deafness	Enrichment	GATA3	2.33
50	Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)	Enrichment	MECOM	2.33
51	Laron syndrome with immunodeficiency	Enrichment	STAT5B	2.33
52	Radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome	Enrichment	MECOM	2.33
53	Type 1 diabetes mellitus 2	Enrichment	INS	2.15
54	End stage renal disease	Enrichment	GATA3	2.15
55	Butterfly-shaped pigment dystrophy	Enrichment	CTNNA1	2.15
56	Melanoma of soft tissue	Enrichment	CREB1	2.15
57	Diffuse gastric and lobular breast cancer syndrome	Enrichment	CTNNA1	2.03
58	Polyposis syndrome, hereditary mixed, 1	Enrichment	CTNNA1	2.03
59	Neonatal diabetes mellitus	Enrichment	INS	2.03
60	Rhabdomyosarcoma 2	Enrichment	FOXO1	1.93
61	Congenital heart defects, multiple types, 4	Enrichment	NR2F2	1.93
62	Gliosarcoma	Enrichment	PPARG	1.89
63	Giant cell glioblastoma	Enrichment	PPARG	1.86
64	Dyskeratosis congenita, autosomal dominant 1	Enrichment	MECOM	1.85
65	Type 1 diabetes mellitus	Enrichment	INS	1.85
66	46,xy disorder of sex development	Enrichment	NR2F2	1.85
67	Charcot-marie-tooth disease type 4	Enrichment	EGR2	1.84
68	Arima syndrome	Enrichment	ZNF423	1.79
69	Dyskeratosis congenita, autosomal dominant 2	Enrichment	MECOM	1.79
70	Colorectal cancer	Enrichment	CTNNA1, PPARG	1.75
71	Permanent neonatal diabetes mellitus	Enrichment	INS	1.73
72	Isolated split hand-split foot malformation	Enrichment	WNT10B	1.73
73	Infantile nephronophthisis	Enrichment	ZNF423	1.73
74	Primary hyperaldosteronism	Enrichment	NR3C1	1.68
75	Hirschsprung disease 1	Enrichment	SREBF1	1.63
76	Differentiated thyroid carcinoma	Enrichment	PPARG	1.63
77	Myelodysplastic syndrome	Enrichment	GATA2	1.59
78	Diabetes mellitus	Enrichment	INS	1.59
79	Multiple sclerosis	Enrichment	NR1H3	1.49
80	Heart disease	Enrichment	NR2F2	1.49
81	Type 2 diabetes mellitus	Enrichment	PPARG	1.47
82	Body mass index quantitative trait locus 11	Enrichment	PPARG	1.40
83	Diffuse large b-cell lymphoma	Enrichment	FOXO1	1.36
84	Maturity-onset diabetes of the young	Enrichment	INS	1.34
85	Craniosynostosis	Enrichment	CTNNA1	1.34
86	Tooth agenesis	Enrichment	WNT10B	1.30
87	Multisystem inflammatory syndrome in children	Enrichment	IRF3	1.30
88	Cakut	Enrichment	GATA3	1.11
89	Thrombocytopenia	Enrichment	MECOM	0.97
90	Hereditary breast ovarian cancer syndrome	Enrichment	CTNNA1	0.91
91	Primary ovarian insufficiency	Enrichment	MECOM	0.88
92	Complex neurodevelopmental disorder	Enrichment	RORA	0.59
93	Hereditary retinal dystrophy	Enrichment	CTNNA1	0.30
94	Fundus dystrophy	Enrichment	CTNNA1	0.30

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

White fat cell differentiation

Pathway Network for White fat cell differentiation

Member Pathways for White fat cell differentiation

Pathways in the White fat cell differentiation SuperPath

Associated Genes for White fat cell differentiation

Associated Disorders for White fat cell differentiation

Disorders associated with White fat cell differentiation SuperPath

STRING Interaction Network for White fat cell differentiation

Sources for White fat cell differentiation