acid phosphatase 1, soluble (ACP1)

Name: ACP1
Description: acid phosphatase 1, soluble
Orgname: Homo sapiens
Status: 0
CurrentID: 0
Chromosome: 2
GeneticSource: genomic
MapLocation: 2p25
OtherAliases: HAAP, MGC111030, MGC3499
OtherDesignations: acid phosphatase of erythrocyte|adipocyte acid phosphatase|cytoplasmic phosphotyrosyl protein phosphatase|low molecular weight phosphotyrosine protein phosphatase|protein tyrosine phosphatase|red cell acid phosphatase 1
NomenclatureSymbol: ACP1
NomenclatureName: acid phosphatase 1, soluble
NomenclatureStatus: Official
TaxID: 9606
GeneWeight: 21992
Summary: The product of this gene belongs to the phosphotyrosine protein phosphatase family of proteins. It functions as an acid phosphatase and a protein tyrosine phosphatase by hydrolyzing protein tyrosine phosphate to protein tyrosine and orthophosphate. This enzyme also hydrolyzes orthophosphoric monoesters to alcohol and orthophosphate. This gene is genetically polymorphic, and three common alleles segregating at the corresponding locus give rise to six phenotypes. Each allele appears to encode at least two electrophoretically different isozymes, Bf and Bs, which are produced in allele-specific ratios. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq]
ChrSort: 02
ChrStart: 264868

UniProtein db: ACP1 UniProt protein knowledge database
Ensembl db: ACP1 Ensembl genome database

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