phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit - Protein

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Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction. [PLoS Genet. 2019]
Mutations in PIK3C2A cause syndromic short stature, skeletal abnormalities, and cataracts associated with ciliary dysfunction.
Tiosano D, Baris HN, Chen A, Hitzert MM, Schueler M, Gulluni F, Wiesener A, Bergua A, Mory A, Copeland B, et al. PLoS Genet. 2019 Apr; 15(4):e1008088. Epub 2019 Apr 29.
Low expression of PIK3C2A gene: A potential biomarker to predict the risk of acute myocardial infarction. [Medicine (Baltimore). 2019]
Low expression of PIK3C2A gene: A potential biomarker to predict the risk of acute myocardial infarction.
Tan B, Liu M, Yang Y, Liu L, Meng F. Medicine (Baltimore). 2019 Apr; 98(14):e15061.
Molecular Basis for Membrane Recruitment by the PX and C2 Domains of Class II Phosphoinositide 3-Kinase-C2α. [Structure. 2018]
Molecular Basis for Membrane Recruitment by the PX and C2 Domains of Class II Phosphoinositide 3-Kinase-C2α.
Chen KE, Tillu VA, Chandra M, Collins BM. Structure. 2018 Dec 4; 26(12):1612-1625.e4. Epub 2018 Oct 4.

RefSeq mRNA
See reference mRNA sequence for the PIK3C2A gene (NM_001386870.1).
RefSeq protein isoforms
See 8 reference sequence protein isoforms for the PIK3C2A gene.

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phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha iso...
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha isoform 3 [Homo sapiens]
gi|1904615211|ref|NP_001373799.1|

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