probable phospholipid-transporting ATPase IM isoform X17 [Homo sapiens - Protein

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Analysis of ATP8B4 F436L Missense Variant in a Large Systemic Sclerosis Cohort. [Arthritis Rheumatol. 2017]
Analysis of ATP8B4 F436L Missense Variant in a Large Systemic Sclerosis Cohort.
López-Isac E, Bossini-Castillo L, Palma AB, Assassi S, Mayes MD, Simeón CP, Ortego-Centeno N, Vicente E, Tolosa C, Rubio-Rivas M, et al. Arthritis Rheumatol. 2017 Jun; 69(6):1337-1338. Epub 2017 May 9.
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing. [Arthritis Rheumatol. 2016]
Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing.
Gao L, Emond MJ, Louie T, Cheadle C, Berger AE, Rafaels N, Vergara C, Kim Y, Taub MA, Ruczinski I, et al. Arthritis Rheumatol. 2016 Jan; 68(1):191-200.
Translocation t(11;14) (q13;q32) and genomic imbalances in multi-ethnic multiple myeloma patients: a Malaysian study. [Hematol Rep. 2012]
Translocation t(11;14) (q13;q32) and genomic imbalances in multi-ethnic multiple myeloma patients: a Malaysian study.
Ni IB, Ching NC, Meng CK, Zakaria Z. Hematol Rep. 2012 Jul 11; 4(3):e19. Epub 2012 Sep 28.

RefSeq mRNA
See reference mRNA sequence for the ATP8B4 gene (XM_011522060.1).
RefSeq protein isoforms
See 85 reference sequence protein isoforms for the ATP8B4 gene.

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Homo sapiens cDNA: FLJ22097 fis, clone HEP17013
Homo sapiens cDNA: FLJ22097 fis, clone HEP17013
gi|10438363|dbj|AK025750.1|

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