RecName: Full=F-actin-capping protein subunit alpha-2; AltName: Full=C - Protein

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Heterozygous CAPZA2 mutations cause global developmental delay, hypotonia with epilepsy: a case report and the literature review. [J Hum Genet. 2024]
Heterozygous CAPZA2 mutations cause global developmental delay, hypotonia with epilepsy: a case report and the literature review.
Zhang XM, Xu KL, Kong JH, Dong G, Dong SJ, Yang ZX, Xu SJ, Wang L, Luo SY, Zhang YD, et al. J Hum Genet. 2024 May; 69(5):197-203. Epub 2024 Feb 19.
Variants in CAPZA2, a member of an F-actin capping complex, cause intellectual disability and developmental delay. [Hum Mol Genet. 2020]
Variants in CAPZA2, a member of an F-actin capping complex, cause intellectual disability and developmental delay.
Huang Y, Mao X, van Jaarsveld RH, Shu L, Terhal PA, Jia Z, Xi H, Peng Y, Yan H, Yuan S, et al. Hum Mol Genet. 2020 Jun 3; 29(9):1537-1546.
Capping protein regulates endosomal trafficking by controlling F-actin density around endocytic vesicles and recruiting RAB5 effectors. [Elife. 2021]
Capping protein regulates endosomal trafficking by controlling F-actin density around endocytic vesicles and recruiting RAB5 effectors.
Wang D, Ye Z, Wei W, Yu J, Huang L, Zhang H, Yue J. Elife. 2021 Nov 19; 10. Epub 2021 Nov 19.

RefSeq protein
See the reference protein sequence for F-actin-capping protein subunit alpha-2 (NP_006127.1).

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P47755 [Domain Mapping of Disease Mut...]
P47755
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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PANTHER Classification System
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ExactAntigen/Labome

RecName: Full=F-actin-capping protein subunit alpha-2; AltName: Full=CapZ alpha-...
RecName: Full=F-actin-capping protein subunit alpha-2; AltName: Full=CapZ alpha-2
gi|1345695|sp|P47755.3|CAZA2_HUMAN

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