PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
Gene ID: 5290, updated on 10-Dec-2024Gene type: protein coding
Also known as: HMH; MCM; CCM4; CWS5; MCAP; PI3K; CLAPO; CLOVE; MCMTC; PI3K-alpha; p110-alpha
- See all available tests in GTR for this gene
- Go to complete Gene record for PIK3CA
- Go to Variation Viewer for PIK3CA variants
Summary
Phosphatidylinositol 3-kinase is composed of an 85 kDa regulatory subunit and a 110 kDa catalytic subunit. The protein encoded by this gene represents the catalytic subunit, which uses ATP to phosphorylate PtdIns, PtdIns4P and PtdIns(4,5)P2. This gene has been found to be oncogenic and has been implicated in cervical cancers. A pseudogene of this gene has been defined on chromosome 22. [provided by RefSeq, Apr 2016]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Cerebral cavernous malformation 4 | not available |
CLAPO syndrome | not available |
CLOVES syndrome | not available |
Colorectal cancer | not available |
Congenital macrodactylia | not available |
Cowden syndrome 5 | not available |
Epidermal nevus | not available |
Familial cancer of breast MedGen: C0346153OMIM: 114480GeneReviews: BRCA1- and BRCA2-Associated Hereditary Breast and Ovarian Cancer | not available |
Gastric cancer | not available |
Hepatocellular carcinoma | not available |
Lung cancer | not available |
Megalencephaly-capillary malformation-polymicrogyria syndrome | not available |
Ovarian neoplasm MedGen: C0919267GeneReviews: Not available | not available |
Seborrheic keratosis | not available |
Copy number response
Description |
---|
Copy number response Haploinsufficency No evidence available (Last evaluated 2015-03-12) ClinGen Genome Curation PageTriplosensitivity No evidence available (Last evaluated 2015-03-12) ClinGen Genome Curation Page |
Genomic context
- Location:
- 3q26.32
- Sequence:
- Chromosome: 3; NC_000003.12 (179148126..179240093)
- Total number of exons:
- 22
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for PIK3CA variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PIK3CA database
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.