Mus musculus ATPase, class VI, type 11A (Atp11a), transcript variant 3 - Nucleotide

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Genetic determinants of micronucleus formation in vivo. [Nature. 2024]
Genetic determinants of micronucleus formation in vivo.
Adams DJ, Barlas B, McIntyre RE, Salguero I, van der Weyden L, Barros A, Vicente JR, Karimpour N, Haider A, Ranzani M, et al. Nature. 2024 Mar; 627(8002):130-136. Epub 2024 Feb 14.
Defects in placental syncytiotrophoblast cells are a common cause of developmental heart disease. [Nat Commun. 2023]
Defects in placental syncytiotrophoblast cells are a common cause of developmental heart disease.
Radford BN, Zhao X, Glazer T, Eaton M, Blackwell D, Mohammad S, Lo Vercio LD, Devine J, Shalom-Barak T, Hallgrimsson B, et al. Nat Commun. 2023 Mar 1; 14(1):1174. Epub 2023 Mar 1.
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2. [Hum Mol Genet. 2023]
A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2.
Chepurwar S, von Loh SM, Wigger DC, Neef J, Frommolt P, Beutner D, Lang-Roth R, Kubisch C, Strenzke N, Volk AE. Hum Mol Genet. 2023 Mar 20; 32(7):1083-1089.

RefSeq protein product
See the reference protein sequence for phospholipid-transporting ATPase IH isoform 3 (NP_001280597.1).

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Mus musculus ATPase, class VI, type 11A (Atp11a), transcript variant 3, mRNA
Mus musculus ATPase, class VI, type 11A (Atp11a), transcript variant 3, mRNA
gi|652697344|ref|NM_001293668.1|

Nucleotide
Mus musculus 10 days embryo whole body cDNA, RIKEN full-length enriched library,...
Mus musculus 10 days embryo whole body cDNA, RIKEN full-length enriched library, clone:2610528D16 product:hypothetical protein, full insert sequence
gi|12848742|dbj|AK012166.1|

Nucleotide
Mus musculus targeted deletion, lacZ-tagged mutant allele Ehmt2:tm1(KOMP)Ucd; tr...
Mus musculus targeted deletion, lacZ-tagged mutant allele Ehmt2:tm1(KOMP)Ucd; transgenic
gi|354794022|gb|JN958523.1|

Nucleotide

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Nucleotide