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Gene : CCNQ Homo sapiens

Name  ? cyclin Q Cytological Location  Xq28
Brief Description  cyclin Q
Description  Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Oct 2008]
  • synonyms:
  • FAM58A,
  • cyclin M,
  • HGNC:28434,
  • NM_152274,
  • CCNQ,
  • family with sequence similarity 58, member A,
  • FAM58A,
  • BC032121,
  • CycM,
  • OTTHUMG00000024206,
  • uc033fau.2,
  • family with sequence similarity 58 member A,
  • CycM
  • identifiers:
  • 92002,
  • ENSG00000262919,
  • CCNQ

Genome feature

Region: gene ? Length: 11241  
Location: X:153587925-153599165 reverse strand Cyto location: Xq28

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

621 SN Ps

5 Cross References

18 Data Sets

4 Homologues

0 Located Features

97 Rna Seq Results