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: 5309
MIM: 602669
HGNC: 9006
Ensembl: ENSG00000107859
Variants:
dbSNP: 5309
ClinVar: 5309
TCGA: ENSG00000107859
COSMIC: PITX3
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000107859 | ENST00000370002 | O75364 |
| ENSG00000107859 | ENST00000539804 | O75364 |
Expression (GTEx)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 34345029 | 2022 | Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts. | 3 |
| 34345029 | 2022 | Variants in PAX6, PITX3 and HSF4 causing autosomal dominant congenital cataracts. | 3 |
| 31310388 | 2020 | Complementation of dopaminergic signaling by Pitx3-GDNF synergy induces dopamine secretion by multipotent Ntera2 cells. | 3 |
| 31310388 | 2020 | Complementation of dopaminergic signaling by Pitx3-GDNF synergy induces dopamine secretion by multipotent Ntera2 cells. | 3 |
| 30816539 | 2019 | PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population. | 4 |
| 30894134 | 2019 | A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract. | 5 |
| 30816539 | 2019 | PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population. | 4 |
| 30894134 | 2019 | A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract. | 5 |
| 29405783 | 2018 | Identification of PITX3 mutations in individuals with various ocular developmental defects. | 10 |
| 29405783 | 2018 | Identification of PITX3 mutations in individuals with various ocular developmental defects. | 10 |
| 27145793 | 2017 | Genetic analysis of PITX3 variants in patients with essential tremor. | 6 |
| 28174607 | 2017 | PITX3 DNA methylation is an independent predictor of overall survival in patients with head and neck squamous cell carcinoma. | 10 |
| 28249924 | 2017 | Whole Exome Sequencing Identifies a Novel Mutation in the PITX3 Gene, Causing Autosomal Dominant Congenital Cataracts in a Chinese Family. | 8 |
| 28991698 | 2017 | PITX3 genotype and risk of dementia in Parkinson's disease: A population-based study. | 5 |
| 27145793 | 2017 | Genetic analysis of PITX3 variants in patients with essential tremor. | 6 |
Citation
Dessen P
PITX3 (paired like homeodomain 3)
Atlas Genet Cytogenet Oncol Haematol. 2016-12-01
Online version: http://atlasgeneticsoncology.org/gene/56649/pitx3-(paired-like-homeodomain-3)
