High affinity Ca2+/Mn2+ P-type ATPase; required for Ca2+ and Mn2+ transport into Golgi; involved in Ca2+ dependent protein sorting, processing; D53A mutant (Mn2+ transporting) is rapamycin sensitive, Q783A mutant (Ca2+ transporting) is rapamycin resistant; Mn2+ transport into Golgi lumen required for rapamycin sensitivity; mutations in human homolog ATP2C1 cause acantholytic skin condition Hailey-Hailey disease; human ATP2C1 can complement yeast null mutant [Source:SGD;Acc:S000003135]

BSD1, LDB1, SSC1

Chromosome VII: 187,616-190,468 reverse strand.

R64-1-1:BK006941.2

This gene has 1 transcript (splice variant), 359 orthologues, 10 paralogues and is a member of 1 Ensembl protein family.

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