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YGL167C / PMR1

Description: High affinity Ca2+/Mn2+ P-type ATPase required for Ca2+ and Mn2+ transport into Golgi; involved in Ca2+ dependent protein sorting and processing; mutations in human homolog ATP2C1 cause acantholytic skin condition Hailey-Hailey disease

Other Aliases: BSD1, SSC1, LDB1

External IDs: S000003135 (sgd),