WNT mediated activation of DVL

No Pathway Network information available for WNT mediated activation of DVL

#	Name	Source	Genes
1	WNT mediated activation of DVL	Reactome	CSNK1E CSNK2A1 CSNK2A2 CSNK2B DVL1 DVL2 DVL3 PIP5K1B (see all 8) (see less)
2	Negative regulation of TCF-dependent signaling by DVL-interacting proteins	Reactome	CCDC88C DVL1 DVL2 DVL3

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

#	Symbol	Description	Category	# Related Pathways
1	DVL1	Dishevelled Segment Polarity Protein 1	Protein Coding	2
2	DVL2	Dishevelled Segment Polarity Protein 2	Protein Coding	2
3	DVL3	Dishevelled Segment Polarity Protein 3	Protein Coding	2
4	CSNK1E	Casein Kinase 1 Epsilon	Protein Coding	1
5	CSNK2A1	Casein Kinase 2 Alpha 1	Protein Coding	1
6	CSNK2A2	Casein Kinase 2 Alpha 2	Protein Coding	1
7	CSNK2B	Casein Kinase 2 Beta	Protein Coding	1
8	PIP5K1B	Phosphatidylinositol-4-Phosphate 5-Kinase Type 1 Beta	Protein Coding	1
9	CCDC88C	Coiled-Coil And HOOK Domain Protein 88C	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Robinow syndrome, autosomal dominant 1	Enrichment	DVL1, DVL3	6.41
2	Autosomal dominant robinow syndrome	Enrichment	DVL1, DVL3	6.41
3	Robinow syndrome, autosomal recessive 1	Enrichment	DVL1, DVL3	6.19
4	Robinow syndrome, autosomal dominant 2	Enrichment	DVL1, DVL3	6.19
5	Autosomal recessive robinow syndrome	Enrichment	DVL1, DVL3	6.01
6	Spinocerebellar ataxia 40	Enrichment	CCDC88C	3.53
7	Robinow syndrome, autosomal dominant 3	Enrichment	DVL3	3.23
8	Okur-chung neurodevelopmental syndrome	Enrichment	CSNK2A1	3.23
9	Craniodigital syndrome and intellectual disability syndrome	Enrichment	CSNK2B	3.23
10	Acyl-coa dehydrogenase, very long-chain, deficiency of	Enrichment	DVL2	2.93
11	Poirier-bienvenu neurodevelopmental syndrome	Enrichment	CSNK2B	2.93
12	Autism spectrum disorder	Enrichment	CSNK2A1, CSNK2B	2.76
13	Prognathism, mandibular	Enrichment	CSNK2B	2.75
14	Congenital hydrocephalus	Enrichment	CCDC88C	2.69
15	Enophthalmos	Enrichment	CSNK2B	2.63
16	Syndactyly	Enrichment	CSNK2B	2.63
17	Hydrocephalus	Enrichment	CCDC88C	2.35
18	Hydrocephalus, congenital, 1	Enrichment	CCDC88C	2.33
19	Developmental and epileptic encephalopathy 1	Enrichment	CSNK1E	1.83
20	Spastic ataxia	Enrichment	CCDC88C	1.81
21	West syndrome	Enrichment	CSNK1E	1.59
22	Autosomal dominant non-syndromic intellectual disability	Enrichment	CSNK2B	1.54
23	Complex neurodevelopmental disorder	Enrichment	CSNK2A1	1.15

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

Pathway Network for WNT mediated activation of DVL