Gene Gene information from NCBI Gene database.
Entrez ID 53
Gene name Acid phosphatase 2, lysosomal
Gene symbol ACP2
Synonyms (NCBI Gene)
LAP
Chromosome 11
Chromosome location 11p11.2|11p12-p11
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 th
miRNA miRNA information provided by mirtarbase database.
490
miRTarBase ID miRNA Experiments Reference
MIRT001481 hsa-miR-16-5p pSILAC 18668040
MIRT023652 hsa-miR-1-3p Proteomics 18668040
MIRT028470 hsa-miR-30a-5p Proteomics 18668040
MIRT001481 hsa-miR-16-5p Proteomics;Other 18668040
MIRT763199 hsa-miR-1260 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
17
GO ID Ontology Definition Evidence Reference
GO:0001501 Process Skeletal system development IEA
GO:0003993 Function Acid phosphatase activity IBA
GO:0003993 Function Acid phosphatase activity IEA
GO:0003993 Function Acid phosphatase activity TAS 3191910
GO:0005515 Function Protein binding IPI 28514442, 32814053, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
171650 123 ENSG00000134575
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P11117
Protein name Lysosomal acid phosphatase (LAP) (EC 3.1.3.2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00328 His_Phos_2 32 330 Histidine phosphatase superfamily (branch 2) Family
Sequence
Sequence length 423
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Riboflavin metabolism
Metabolic pathways
Lysosome
 
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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
ANTI-NMDA RECEPTOR ENCEPHALITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTENSION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Anti N Methyl D Aspartate Receptor Encephalitis Associate 34584012
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 15967798
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 28076332
★☆☆☆☆
Found in Text Mining only
Drug Hypersensitivity Associate 25633562
★☆☆☆☆
Found in Text Mining only
Lysosomal Storage Diseases Associate 17357082
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 36706181
★☆☆☆☆
Found in Text Mining only
Supranuclear Palsy Progressive Associate 17357082
★☆☆☆☆
Found in Text Mining only