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Gene: CCNQ (cyclin Q) Homo sapiens
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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
Orthologs:
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
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
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)
Model


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

Genomics

Comparative Map Data
Position Markers

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on CCNQ
Alliance Gene
NCBI 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



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