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ACP2

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Protein-coding gene in humans
ACP2
Identifiers
AliasesACP2, acid phosphatase 2, lysosomal, LAP
External IDsOMIM: 171650; MGI: 87882; HomoloGene: 1217; GeneCards: ACP2; OMA:ACP2 - orthologs
Gene location (Human)
Chromosome 11 (human)
Chr.Chromosome 11 (human)
Chromosome 11 (human)Genomic location for ACP2Genomic location for ACP2
Band11p11.2|11p12-p11Start47,239,302 bp
End47,248,906 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for ACP2Genomic location for ACP2
Band2 E1|2 50.54 cMStart91,033,230 bp
End91,044,443 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • right lobe of liver

  • body of pancreas

  • right adrenal gland

  • left adrenal gland

  • right adrenal cortex

  • stromal cell of endometrium

  • jejunal mucosa

  • left adrenal cortex

  • mucosa of transverse colon

  • salivary gland
Top expressed in
  • spermatocyte

  • medial dorsal nucleus

  • stroma of bone marrow

  • spermatid

  • dentate gyrus of hippocampal formation granule cell

  • choroid plexus of fourth ventricle

  • medial geniculate nucleus

  • ascending aorta

  • aortic valve

  • genital tubercle
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

53

11432

Ensembl

ENSG00000134575

ENSMUSG00000002103

UniProt

P11117

P24638

RefSeq (mRNA)
NM_001131064
NM_001302489
NM_001302490
NM_001302491
NM_001302492

NM_001610
NM_001357016

NM_007387
NM_001357067

RefSeq (protein)
NP_001289418
NP_001289419
NP_001289420
NP_001289421
NP_001601

NP_001343945

NP_031413
NP_001343996

Location (UCSC)Chr 11: 47.24 – 47.25 MbChr 2: 91.03 – 91.04 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Lysosomal acid phosphatase is an enzyme that in humans is encoded by the ACP2 gene.

Lysosomal acid phosphatase is composed of two subunits, alpha and beta, and is chemically and genetically distinct from red cell acid phosphatase. Lysosomal acid phosphatase 2 is a member of a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Acid phosphatase deficiency is caused by mutations in the ACP2 (beta subunit) and ACP3 (alpha subunit) genes.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000134575Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000002103Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Shows TB, Brown JA, Lalley PA (Dec 1976). "Assignment and linear order of human acid phosphatase-2, esterase A4, and lactate dehydrogenase A genes on chromosome 11". Cytogenet Cell Genet. 16 (1–5): 231–4. doi:10.1159/000130598. PMID 975882.
  6. ^ "Entrez Gene: ACP2 acid phosphatase 2, lysosomal".

Further reading

External links

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