Acp2 - acid phosphatase 2, lysosomal Gene
Also Known as LAP; Acp-2
Species: Mus musculus
Summary
The protein encoded by this gene belongs to the histidine Acid Phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell Acid Phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Two isoforms are predicted to be produced from the same mRNA by the use of alternative in-frame translation termination codons via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2017]
Acp2 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_001357067.1 | NP_001343996.1 | lysosomal acid phosphatase isoform 1x precursor |
| NM_007387.2 | NP_031413.1 | lysosomal acid phosphatase isoform 1 precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables acid phosphatase activity |
IDA
IDA: Inferred from direct assay
|
1914521 | MGI |
| enables acid phosphatase activity |
IMP
IMP: Inferred from mutant phenotype
|
9228031 | MGI |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| acts upstream of or within lysosome organization |
IMP
IMP: Inferred from mutant phenotype
|
9228031 | MGI |
| acts upstream of or within skeletal system development |
IMP
IMP: Inferred from mutant phenotype
|
9228031 | MGI |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| located in lysosome |
IDA
IDA: Inferred from direct assay
|
11168643 | MGI |
| located in lysosome |
IMP
IMP: Inferred from mutant phenotype
|
11731469 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
lysosomal acid phosphatase |
|