Disease table of GALLOWAY-MOWAT SYNDROME OMIM ID: 251300

Gene-disease associations table

GeneAssociated with GALLOWAY-MOWAT SYNDROME inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
ZNF592ClinVarHGNC link15q25.31251300
WDR73ClinVar, OMIMHGNC link15q25.21251300

Download the disease annotation in CSV format

Relations among genes:

Tandem repeat annotations from DGD
Cytogenetic band analysis
By band
Shared bandNumber of genes associated with the diseaseGenes associated with the disease
15q252ZNF592, WDR73
By region
Shared regionNumber of genes associated with the diseaseGenes associated with the disease
15q22ZNF592, WDR73
By arm
Shared armNumber of genes associated with the diseaseGenes associated with the disease
15q2ZNF592, WDR73
By chromosome
Shared chromosomeNumber of genes associated with the diseaseGenes associated with the disease
152ZNF592, WDR73
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 (no NET-GE enrichment)

Shared terms

GOICNumber of genes with the same GOGenes
intracellular part (GO:0044424) 0.282WDR73, ZNF592
intracellular organelle (GO:0043229) 0.512WDR73, ZNF592
cell part (GO:0044464) 0.112WDR73, ZNF592
organelle (GO:0043226) 0.42WDR73, ZNF592