Gene Gene information from NCBI Gene database.
Entrez ID 390928
Gene name Acid phosphatase 7, tartrate resistant (putative)
Gene symbol ACP7
Synonyms (NCBI Gene)
PAPLPAPL1
Chromosome 19
Chromosome location 19q13.2
Summary Purple acid phosphatases (PAPs), including PAPL, are a family of binuclear metallohydrolases that have been identified in plants, animals, and fungi (Flanagan et al., 2006 [PubMed 16793224]).[supplied by OMIM, Mar 2008]
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0003993 Function Acid phosphatase activity IEA
GO:0005576 Component Extracellular region IEA
GO:0016787 Function Hydrolase activity IEA
GO:0046872 Function Metal ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
610490 33781 ENSG00000183760
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZNF0
Protein name Acid phosphatase type 7 (EC 3.1.3.2) (Purple acid phosphatase long form)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF16656 Pur_ac_phosph_N 32 125 Purple acid Phosphatase, N-terminal domain Domain
PF00149 Metallophos 134 337 Calcineurin-like phosphoesterase Domain
PF14008 Metallophos_C 362 424 Iron/zinc purple acid phosphatase-like protein C Domain
Sequence
Sequence length 438
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations