ATPase family gene 2 protein homolog A isoform 2 [Homo sapiens]

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Isolated Hearing Impairment Caused by SPATA5 Mutations in a Family with Variable Phenotypic Expression. [Adv Exp Med Biol. 2017]
Isolated Hearing Impairment Caused by SPATA5 Mutations in a Family with Variable Phenotypic Expression.
Szczałuba K, Szymańska K, Kosińska J, Pollak A, Murcia V, Kędra A, Stawiński P, Rydzanicz M, Demkow U, Płoski R. Adv Exp Med Biol. 2017; 980:59-66.
Characterization of SPATA5-related encephalopathy in early childhood. [Clin Genet. 2016]
Characterization of SPATA5-related encephalopathy in early childhood.
Kurata H, Terashima H, Nakashima M, Okazaki T, Matsumura W, Ohno K, Saito Y, Maegaki Y, Kubota M, Nanba E, et al. Clin Genet. 2016 Nov; 90(5):437-444. Epub 2016 Jul 4.
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata. [Eur J Hum Genet. 2012]
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata.
Forstbauer LM, Brockschmidt FF, Moskvina V, Herold C, Redler S, Herzog A, Hillmer AM, Meesters C, Heilmann S, Albert F, et al. Eur J Hum Genet. 2012 Mar; 20(3):326-32. Epub 2011 Oct 26.

RefSeq genomic sequence
See the genomic reference sequence for the AFG2A gene (NG_051570.1).
RefSeq protein isoforms
See 31 reference sequence protein isoforms for the AFG2A gene.

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein