Entity Details

Primary name CDCA7
Entity type gene
Source Source Link

Details

PrimaryID83879
RefseqGeneNG_047202
SymbolCDCA7
Namecell division cycle associated 7
Chromosome2
Location2q31.1
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2001-05-06
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCDCA7_HUMAN

GO terms

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GOName
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005829 cytosol
GO:0006355 regulation of transcription, DNA-templated
GO:0006915 apoptotic process
GO:0042127 regulation of cell population proliferation

Diseases

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Disease IDSourceNameDescription
616910 OMIMImmunodeficiency-centromeric instability-facial anomalies syndrome 3 (ICF3)A rare disorder characterized by a variable immunodeficiency resulting in recurrent infections, facial anomalies, and branching of chromosomes 1, 9, and 16. Other variable symptoms include growth retardation, failure to thrive, and psychomotor retardation. Laboratory studies show limited hypomethylation of DNA in a small fraction of the genome in some, but not all, patients. The disease may be caused by variants affecting the gene represented in this entry.

Interactions

10 interactions