Disease table of HYDROLETHALUS SYNDROME OMIM ID: PS236680

Gene-disease associations table

GeneAssociated with HYDROLETHALUS SYNDROME inLink to HGNCCytogenetic bandNumber of associated diseasesAssociated diseases
KIF7OMIM, HUMSAVARHGNC link15q26.15146510, PS236680, PS209900, 607131, PS213300
HYLS1OMIM, HUMSAVARHGNC link11q24.21PS236680

Download the disease annotation in CSV format

Relations among genes:

Tandem repeat annotations from DGD
Cytogenetic band analysis
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 (no NET-GE enrichment)

Shared terms

GOICNumber of genes with the same GOGenes
binding (GO:0005488) 0.182HYLS1, KIF7
protein binding (GO:0005515) 0.462HYLS1, KIF7
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
cell part (GO:0044464) 0.112HYLS1, KIF7
intracellular organelle part (GO:0044446) 0.812HYLS1, KIF7
cytoskeletal part (GO:0044430) 2.492HYLS1, KIF7
intracellular part (GO:0044424) 0.282HYLS1, KIF7
organelle (GO:0043226) 0.42HYLS1, KIF7
organelle part (GO:0044422) 0.792HYLS1, KIF7