Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

No Pathway Network information available for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Pathways in the Regulation of CDH1 posttranslational processing and trafficking to plasma membrane SuperPath

#	Name	Source	Genes
1	Regulation of CDH1 posttranslational processing and trafficking to plasma membrane	Reactome	ANK3 ARHGAP32 CANX CSNK2A1 CSNK2A2 CSNK2A3 CSNK2B CTNNB1 DAD1 DDOST FURIN GANAB JUP MOGS OST4 OSTC PCSK6 PCSK7 PIP5K1C POMT1 POMT2 PRKCSH RPN1 RPN2 SEC11A SEC11C SPCS1 SPCS2 SPCS3 STT3A TMEM258 (see all 31) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	OST4	Oligosaccharyltransferase Complex Subunit 4, Non-Catalytic	Protein Coding	1
2	POMT1	Protein O-Mannosyltransferase 1	Protein Coding	1
3	CSNK2A1	Casein Kinase 2 Alpha 1	Protein Coding	1
4	CSNK2A2	Casein Kinase 2 Alpha 2	Protein Coding	1
5	CSNK2B	Casein Kinase 2 Beta	Protein Coding	1
6	CTNNB1	Catenin Beta 1	Protein Coding	1
7	DAD1	Defender Against Cell Death 1	Protein Coding	1
8	DDOST	Dolichyl-Diphosphooligosaccharide--Protein Glycosyltransferase Non-Catalytic Subunit	Protein Coding	1
9	GANAB	Glucosidase II Alpha Subunit	Protein Coding	1
10	PIP5K1C	Phosphatidylinositol-4-Phosphate 5-Kinase Type 1 Gamma	Protein Coding	1
11	SEC11A	SEC11 Homolog A, Signal Peptidase Complex Subunit	Protein Coding	1
12	CSNK2A3	Casein Kinase 2 Alpha 3	Protein Coding	1
13	ANK3	Ankyrin 3	Protein Coding	1
14	SPCS1	Signal Peptidase Complex Subunit 1	Protein Coding	1
15	POMT2	Protein O-Mannosyltransferase 2	Protein Coding	1
16	STT3A	STT3 Oligosaccharyltransferase Complex Catalytic Subunit A	Protein Coding	1
17	JUP	Junction Plakoglobin	Protein Coding	1
18	FURIN	Furin, Paired Basic Amino Acid Cleaving Enzyme	Protein Coding	1
19	PCSK6	Proprotein Convertase Subtilisin/Kexin Type 6	Protein Coding	1
20	PRKCSH	PRKCSH Beta Subunit Of Glucosidase II	Protein Coding	1
21	OSTC	Oligosaccharyltransferase Complex Non-Catalytic Subunit	Protein Coding	1
22	SPCS3	Signal Peptidase Complex Subunit 3	Protein Coding	1
23	RPN1	Ribophorin I	Protein Coding	1
24	RPN2	Ribophorin II	Protein Coding	1
25	TMEM258	Transmembrane Protein 258	Protein Coding	1
26	MOGS	Mannosyl-Oligosaccharide Glucosidase	Protein Coding	1
27	CANX	Calnexin	Protein Coding	1
28	SEC11C	SEC11 Homolog C, Signal Peptidase Complex Subunit	Protein Coding	1
29	PCSK7	Proprotein Convertase Subtilisin/Kexin Type 7	Protein Coding	1
30	ARHGAP32	Rho GTPase Activating Protein 32	Protein Coding	1
31	SPCS2	Signal Peptidase Complex Subunit 2	Protein Coding	1

Disorders associated with Regulation of CDH1 posttranslational processing and trafficking to plasma membrane SuperPath

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Polycystic liver disease	Enrichment	CTNNB1, GANAB, PRKCSH	5.14
2	Autosomal dominant polycystic liver disease	Enrichment	CTNNB1, GANAB, PRKCSH	5.14
3	Muscular dystrophy-dystroglycanopathy , type a, 1	Enrichment	POMT1, POMT2	4.30
4	Congenital muscular dystrophy with intellectual disability	Enrichment	POMT1, POMT2	4.30
5	Congenital muscular dystrophy with cerebellar involvement	Enrichment	POMT1, POMT2	4.12
6	Muscle eye brain disease	Enrichment	POMT1, POMT2	3.65
7	Medulloblastoma	Enrichment	ANK3, CTNNB1	3.34
8	Walker-warburg syndrome	Enrichment	POMT1, POMT2	3.34
9	Autosomal recessive limb-girdle muscular dystrophy	Enrichment	POMT1, POMT2	3.07
10	Congenital nervous system abnormality	Enrichment	ANK3, CTNNB1, POMT1	2.75
11	Nervous system disease	Enrichment	ANK3, CTNNB1, POMT1	2.75
12	Arrhythmogenic right ventricular dysplasia, familial, 12	Enrichment	JUP	2.64
13	Intellectual developmental disorder, autosomal recessive 37	Enrichment	ANK3	2.64
14	Congenital disorder of glycosylation, type iw, autosomal recessive	Enrichment	STT3A	2.64
15	Muscular dystrophy-dystroglycanopathy , type b, 1	Enrichment	POMT1	2.64
16	Naxos disease	Enrichment	JUP	2.64
17	Muscular dystrophy-dystroglycanopathy , type c, 1	Enrichment	POMT1	2.64
18	Congenital disorder of glycosylation, type ir	Enrichment	DDOST	2.64
19	Okur-chung neurodevelopmental syndrome	Enrichment	CSNK2A1	2.64
20	Adenoid ameloblastoma	Enrichment	CTNNB1	2.64
21	Congenital disorder of glycosylation iw	Enrichment	STT3A	2.64
22	Craniodigital syndrome and intellectual disability syndrome	Enrichment	CSNK2B	2.64
23	Microcystic stromal tumor	Enrichment	CTNNB1	2.64
24	Osteopathia striata with cranial sclerosis	Enrichment	CTNNB1	2.34
25	Lethal congenital contracture syndrome 3	Enrichment	PIP5K1C	2.34
26	Congenital disorder of glycosylation, type iib	Enrichment	MOGS	2.34
27	Muscular dystrophy-dystroglycanopathy , type c, 12	Enrichment	POMT1	2.34
28	Muscular dystrophy-dystroglycanopathy , type c, 2	Enrichment	POMT2	2.34
29	Muscular dystrophy-dystroglycanopathy , type a, 2	Enrichment	POMT2	2.34
30	Poirier-bienvenu neurodevelopmental syndrome	Enrichment	CSNK2B	2.34
31	Childhood hepatocellular carcinoma	Enrichment	CTNNB1	2.34
32	Muscular dystrophy-dystroglycanopathy , type b, 2	Enrichment	POMT2	2.34
33	Congenital disorder of glycosylation, type iw, autosomal dominant	Enrichment	STT3A	2.34
34	Polycystic kidney disease 3	Enrichment	GANAB	2.34
35	Juvenile nasopharyngeal angiofibroma	Enrichment	CTNNB1	2.34
36	Teratoma	Enrichment	CTNNB1	2.34
37	Acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2)	Enrichment	RPN1	2.34
38	Desmoid disease, hereditary	Enrichment	CTNNB1	2.16
39	Prognathism, mandibular	Enrichment	CSNK2B	2.16
40	Epidermolysis bullosa, lethal acantholytic	Enrichment	JUP	2.16
41	Neurodevelopmental disorder with spastic diplegia and visual defects	Enrichment	CTNNB1	2.16
42	Anus, imperforate	Enrichment	CTNNB1	2.16
43	Exudative vitreoretinopathy 7	Enrichment	CTNNB1	2.16
44	Desmoid tumor	Enrichment	CTNNB1	2.16
45	Congenital muscular dystrophy-dystroglycanopathy type a	Enrichment	POMT2	2.16
46	Pilomatrixoma	Enrichment	CTNNB1	2.04
47	Alazami syndrome	Enrichment	CTNNB1	2.04
48	Enophthalmos	Enrichment	CSNK2B	2.04
49	Syndactyly	Enrichment	CSNK2B	2.04
50	Craniopharyngioma	Enrichment	CTNNB1	2.04
51	Congenital muscular dystrophy without intellectual disability	Enrichment	POMT1	2.04
52	Polycystic liver disease 1 with or without kidney cysts	Enrichment	PRKCSH	1.94
53	Exudative vitreoretinopathy 1	Enrichment	CTNNB1	1.94
54	Polycystic kidney disease 3 with or without polycystic liver disease	Enrichment	GANAB	1.94
55	Polycystic liver disease 1	Enrichment	PRKCSH	1.94
56	Weyers acrofacial dysostosis	Enrichment	CTNNB1	1.87
57	Adrenocortical carcinoma	Enrichment	CTNNB1	1.87
58	Gallbladder cancer	Enrichment	CTNNB1	1.80
59	Exudative vitreoretinopathy	Enrichment	CTNNB1	1.74
60	Adult hepatocellular carcinoma	Enrichment	CTNNB1	1.69
61	Autism spectrum disorder	Enrichment	CSNK2A1, CSNK2B	1.59
62	Inherited isolated arrhythmogenic ventricular dysplasia, biventricular variant	Enrichment	JUP	1.57
63	Inherited isolated arrhythmogenic cardiomyopathy, dominant-left variant	Enrichment	JUP	1.57
64	Inherited isolated arrhythmogenic cardiomyopathy, dominant-right variant	Enrichment	JUP	1.50
65	Autosomal dominant polycystic kidney disease	Enrichment	GANAB	1.47
66	Wolff-parkinson-white syndrome	Enrichment	JUP	1.44
67	Hydrocephalus, congenital, 1	Enrichment	POMT1	1.44
68	Arrhythmogenic right ventricular cardiomyopathy	Enrichment	JUP	1.44
69	Hepatoblastoma	Enrichment	CTNNB1	1.33
70	Hepatocellular carcinoma	Enrichment	CTNNB1	1.31
71	Muscular dystrophy	Enrichment	POMT2	1.27
72	Bladder cancer	Enrichment	CTNNB1	1.19
73	Autosomal dominant non-syndromic intellectual disability	Enrichment	CSNK2B	0.97
74	Dilated cardiomyopathy	Enrichment	JUP	0.78
75	Colorectal cancer	Enrichment	CTNNB1	0.74
76	Ovarian cancer	Enrichment	CTNNB1	0.68
77	Microcephaly	Enrichment	CTNNB1	0.61
78	Complex neurodevelopmental disorder	Enrichment	CSNK2A1	0.61

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

Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Pathway Network for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Member Pathways for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Pathways in the Regulation of CDH1 posttranslational processing and trafficking to plasma membrane SuperPath

Associated Genes for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Associated Disorders for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Disorders associated with Regulation of CDH1 posttranslational processing and trafficking to plasma membrane SuperPath

STRING Interaction Network for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane

Sources for Regulation of CDH1 posttranslational processing and trafficking to plasma membrane