Disease table of VAN DER WOUDE SYNDROME 2 OMIM ID: 606713

Gene-disease associations table

Gene	Associated with VAN DER WOUDE SYNDROME 2 in	Link to HGNC	Cytogenetic band	Number of associated diseases	Associated diseases
CFAP57	ClinVar	HGNC link	1p34.2	1	606713
GRHL3	ClinVar, OMIM, HUMSAVAR	HGNC link	1p36.11	1	606713

Tandem repeat annotations from DGD

Cytogenetic band analysis

By region

Shared region	Number of genes associated with the disease	Genes associated with the disease
1p3	2	GRHL3, CFAP57

By arm

Shared arm	Number of genes associated with the disease	Genes associated with the disease
1p	2	GRHL3, CFAP57

By chromosome

Shared chromosome	Number of genes associated with the disease	Genes associated with the disease
1	2	GRHL3, CFAP57

Transcription Factors (TF) annotation from TRRUST

Interactions from BIOGRID - physical

Interactions from BIOGRID - genetic

Interactions from STRING

Interactions from CORUM

Interactions from CENSUS

Interactions from PDB

Interactions from manually curated literature

KEGG pathways annotation: shared terms / NET-GE enrichment (no shared terms)

REACTOME pathways annotation: shared terms / NET-GE enrichment (no shared terms)

GO - molecular function annotation: shared terms / NET-GE enrichment (no shared terms)

GO - biological process annotation: shared terms / NET-GE enrichment (no shared terms)

GO - cellular component annotation: shared terms / NET-GE enrichment (no shared terms)