Gene-disease associations table
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Gene Associated with SECKEL SYNDROME in Link to HGNC Cytogenetic band Number of associated diseases Associated diseases ATR ClinVar, OMIM HGNC link 3q23 2 614564 , PS210600 CENPJ ClinVar, OMIM HGNC link 13q12.13 2 PS251200 , PS210600 CEP152 ClinVar, OMIM, HUMSAVAR HGNC link 15q21.1 2 PS251200 , PS210600 CEP63 ClinVar, OMIM HGNC link 3q22.2 1 PS210600 DNA2 OMIM HGNC link 10q21.3 2 PS157640 , PS210600 NIN ClinVar, OMIM, HUMSAVAR HGNC link 14q22.1 1 PS210600 RBBP8 ClinVar, OMIM, HUMSAVAR HGNC link 18q11.2 3 251255 , 260350 , PS210600 TRAIP ClinVar, OMIM HGNC link 3p21.31 1 PS210600
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Relations among genes:
Tandem repeat annotations from DGD
Cytogenetic band analysis
By region
By arm
By chromosome
Transcription Factors (TF) annotation from TRRUST
Interactions from BIOGRID - physical
Direct interactions graph
Interactions graph (direct and indirect interactions, when direct are not available)
Interactions from BIOGRID - genetic
Interactions from STRING
Direct interactions graph
Interactions graph (direct and indirect interactions, when direct are not available)
Interactions from CORUM
Interactions from CENSUS
Interactions from PDB
Interactions from manually curated literature
KEGG pathways annotation: NET-GE enrichment (no shared terms)
NET-GE enrichment
REACTOME pathways annotation: shared terms / NET-GE enrichment
Shared terms
NET-GE enrichment
GO - molecular function annotation: shared terms / NET-GE enrichment
Shared terms
NET-GE enrichment
GO - biological process annotation: shared terms / NET-GE enrichment
Shared terms
NET-GE enrichment
GO - cellular component annotation: shared terms / NET-GE enrichment
Shared terms
NET-GE enrichment