Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: CCNQ (cyclin Q) Homo sapiens
Symbol: CCNQ
Name: 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]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: CDK10-activating cyclin; cyclin M; cyclin-M; cyclin-Q; cyclin-related protein FAM58A; FAM58A; family with sequence similarity 58 member A; family with sequence similarity 58, member A; MGC29729; STAR
Mus musculus (house mouse) : Ccnq (cyclin Q)  MGI  Alliance
Rattus norvegicus (Norway rat) : Ccnq (cyclin Q)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Ccnq (cyclin Q)
Pan paniscus (bonobo/pygmy chimpanzee) : CCNQ (cyclin Q)
Canis lupus familiaris (dog) : CCNQ (cyclin Q)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Ccnq (cyclin Q)
Sus scrofa (pig) : CCNQ (cyclin Q)
more info ...
Related Pseudogenes: CCNQP1   CCNQP2   CCNQP3  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Human AssemblyChrPosition (strand)SourceGenome Browsers
GRCh38X153,587,925 - 153,599,177 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X152,853,383 - 152,864,632 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X152,506,577 - 152,517,775 (-)NCBINCBI36hg18NCBI36
CeleraX153,087,076 - 153,098,328 (-)NCBI
Cytogenetic MapXq28NCBI
HuRefX141,511,974 - 141,519,982 (-)NCBIHuRef
CHM1_1X152,727,894 - 152,739,153 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)

Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated


Comparative Map Data
Position Markers


Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
More on CCNQ
Alliance Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1604257
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2019-06-18
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.