Identity
HGNC
LOCATION
10p12.1
LOCUSID
ALIAS
THC2,bA145E8.1
FUSION GENES
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: 22852
MIM: 610855
HGNC: 29186
Ensembl: ENSG00000107890
Variants:
dbSNP: 22852
ClinVar: 22852
TCGA: ENSG00000107890
COSMIC: ANKRD26
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000107890 | ENST00000376087 | Q9UPS8 |
| ENSG00000107890 | ENST00000436985 | E7ESJ3 |
| ENSG00000107890 | ENST00000445828 | H0Y4T9 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36626254 | 2023 | Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26. | 11 |
| 36626254 | 2023 | Hereditary platelet disorders associated with germ line variants in RUNX1, ETV6, and ANKRD26. | 11 |
| 35537115 | 2022 | Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations. | 8 |
| 35587581 | 2022 | Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases. | 4 |
| 35751752 | 2022 | ANKRD26-Related Thrombocytopenia and Predisposition to Myeloid Neoplasms. | 6 |
| 35796010 | 2022 | Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations. | 2 |
| 35537115 | 2022 | Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations. | 8 |
| 35587581 | 2022 | Prevalence and natural history of variants in the ANKRD26 gene: a short review and update of reported cases. | 4 |
| 35751752 | 2022 | ANKRD26-Related Thrombocytopenia and Predisposition to Myeloid Neoplasms. | 6 |
| 35796010 | 2022 | Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations. | 2 |
| 32659145 | 2021 | Relation between mutations in the 5' UTR of ANKRD26 gene and inherited thrombocytopenia with predisposition to myeloid malignancies. An Egyptian study. | 2 |
| 32944898 | 2021 | A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome. | 2 |
| 33857290 | 2021 | Familial thrombocytopenia due to a complex structural variant resulting in a WAC-ANKRD26 fusion transcript. | 12 |
| 32659145 | 2021 | Relation between mutations in the 5' UTR of ANKRD26 gene and inherited thrombocytopenia with predisposition to myeloid malignancies. An Egyptian study. | 2 |
| 32944898 | 2021 | A novel RUNX1 mutation with ANKRD26 dysregulation is related to thrombocytopenia in a sporadic form of myelodysplastic syndrome. | 2 |
Citation
Dessen P
ANKRD26 (ankyrin repeat domain 26)
Atlas Genet Cytogenet Oncol Haematol. 2016-10-01
Online version: http://atlasgeneticsoncology.org/gene/55967/ankrd26-(ankyrin-repeat-domain-26)
