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: 5277
MIM: 311770
HGNC: 8957
Ensembl: ENSG00000165195
Variants:
dbSNP: 5277
ClinVar: 5277
TCGA: ENSG00000165195
COSMIC: PIGA
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37271276 | 2023 | PIG-A gene mutation as a mutagenicity biomarker among coke oven workers. | 1 |
| 37589195 | 2023 | Congenital diaphragmatic hernia in siblings with PIGA-related congenital disorder of glycosylation. | 0 |
| 37271276 | 2023 | PIG-A gene mutation as a mutagenicity biomarker among coke oven workers. | 1 |
| 37589195 | 2023 | Congenital diaphragmatic hernia in siblings with PIGA-related congenital disorder of glycosylation. | 0 |
| 34875027 | 2022 | Constitutional PIGA mutations cause a novel subtype of hemochromatosis in patients with neurologic dysfunction. | 3 |
| 34875027 | 2022 | Constitutional PIGA mutations cause a novel subtype of hemochromatosis in patients with neurologic dysfunction. | 3 |
| 33169419 | 2021 | Evaluation of PIG-A-mutated granulocytes and ex-vivo binucleated micronucleated lymphocytes frequencies after breast cancer radiotherapy in humans. | 1 |
| 33483614 | 2021 | Implication of PIGA genotype on erythrocytes phenotype in Paroxysmal Nocturnal Hemoglobinuria. | 7 |
| 33169419 | 2021 | Evaluation of PIG-A-mutated granulocytes and ex-vivo binucleated micronucleated lymphocytes frequencies after breast cancer radiotherapy in humans. | 1 |
| 33483614 | 2021 | Implication of PIGA genotype on erythrocytes phenotype in Paroxysmal Nocturnal Hemoglobinuria. | 7 |
| 32359022 | 2020 | Identification of acquired PIGA mutations and additional variants by next-generation sequencing in paroxysmal nocturnal hemoglobinuria. | 5 |
| 32452540 | 2020 | Lessons learned from 40 novel PIGA patients and a review of the literature. | 24 |
| 32562213 | 2020 | PIGA-related epileptic encephalopathy demonstrating intrafamilial phenotypic heterogeneity. | 0 |
| 32694024 | 2020 | Early-onset epileptic encephalopathy related to germline PIGA mutations: A series of 5 cases. | 1 |
| 32875608 | 2020 | Mutations in PIGA cause a CD52-/GPI-anchor-deficient phenotype complicating alemtuzumab treatment in T-cell prolymphocytic leukemia. | 2 |
Citation
Dessen P
PIGA (phosphatidylinositol glycan anchor biosynthesis class A)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/47443/piga-(phosphatidylinositol-glycan-anchor-biosynthesis-class-a)
