Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 53
MIM: 171650
HGNC: 123
Ensembl: ENSG00000134575
Variants:
dbSNP: 53
ClinVar: 53
TCGA: ENSG00000134575
COSMIC: ACP2
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Riboflavin metabolism | KEGG | ko00740 |
| Riboflavin metabolism | KEGG | hsa00740 |
| Lysosome | KEGG | ko04142 |
| Lysosome | KEGG | hsa04142 |
| Metabolic pathways | KEGG | hsa01100 |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33381921 | 2021 | Clinical and molecular evaluation of 13 Brazilian patients with Gomez-López-Hernández syndrome. | 3 |
| 33381921 | 2021 | Clinical and molecular evaluation of 13 Brazilian patients with Gomez-López-Hernández syndrome. | 3 |
| 29422769 | 2018 | A genome-wide association study of corneal astigmatism: The CREAM Consortium. | 9 |
| 29422769 | 2018 | A genome-wide association study of corneal astigmatism: The CREAM Consortium. | 9 |
| 28076332 | 2017 | Lysosomal acid phosphatase 2 is an unfavorable prognostic factor but is associated with better survival in stage II colorectal cancer patients receiving chemotherapy. | 1 |
| 28076332 | 2017 | Lysosomal acid phosphatase 2 is an unfavorable prognostic factor but is associated with better survival in stage II colorectal cancer patients receiving chemotherapy. | 1 |
| 19064571 | 2008 | Polymorphisms in mitochondrial genes and prostate cancer risk. | 22 |
| 19064571 | 2008 | Polymorphisms in mitochondrial genes and prostate cancer risk. | 22 |
| 17357082 | 2007 | Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. | 29 |
| 17357082 | 2007 | Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. | 29 |
| 15503243 | 2004 | Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse. | 21 |
| 15503243 | 2004 | Mutation in the gene encoding lysosomal acid phosphatase (Acp2) causes cerebellum and skin malformation in mouse. | 21 |
| 9228031 | 1997 | Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system. | 20 |
| 9228031 | 1997 | Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system. | 20 |
Citation
Dessen P
ACP2 (acid phosphatase 2, lysosomal)
Atlas Genet Cytogenet Oncol Haematol. 2003-11-01
Online version: http://atlasgeneticsoncology.org/gene/554/acp2
