Entity Details

Primary name CCNQ_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ8N1B3
EntryNameCCNQ_HUMAN
FullNameCyclin-Q
TaxID9606
Evidenceevidence at protein level
Length248
SequenceStatuscomplete
DateCreated2007-08-21
DateModified2021-06-02

Ontological Relatives

GenesCCNQ

GO terms

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GOName
GO:0005634 nucleus
GO:0006357 regulation of transcription by RNA polymerase II
GO:0016538 cyclin-dependent protein serine/threonine kinase regulator activity

Subcellular Location

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Domains

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DomainNameCategoryType
IPR006671 Cyclin, N-terminalDomainDomain
IPR013763 Cyclin-likeDomainDomain
IPR028759 Cyclin-QFamilyFamily
IPR036915 Cyclin-like superfamilyFamilyHomologous superfamily
IPR043198 Cyclin/Cyclin-like subunit Ssn8FamilyFamily

Diseases

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Disease IDSourceNameDescription
300707 OMIMToe syndactyly, telecanthus, and anogenital and renal malformations (STAR)A syndrome characterized by anal, genital and renal tract anomalies, facial dysmorphism and syndactyly. Features include anal stenosis, a rectovaginal fistula, clitoral hypertrophy, a pelvic right kidney, toe syndactyly, and telecanthus. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions