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: 286
MIM: 612641
HGNC: 492
Ensembl: ENSG00000029534
Variants:
dbSNP: 286
ClinVar: 286
TCGA: ENSG00000029534
COSMIC: ANK1
RNA/Proteins
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38862513 | 2024 | Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes. | 0 |
| 38862513 | 2024 | Whole-genome sequencing identifies variants in ANK1, LRRN1, HAS1, and other genes and regulatory regions for stroke in type 1 diabetes. | 0 |
| 36336297 | 2023 | A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family. | 2 |
| 36598564 | 2023 | Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. | 0 |
| 36647015 | 2023 | De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing. | 1 |
| 37341850 | 2023 | Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans. | 0 |
| 36336297 | 2023 | A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family. | 2 |
| 36598564 | 2023 | Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum. | 0 |
| 36647015 | 2023 | De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing. | 1 |
| 37341850 | 2023 | Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans. | 0 |
| 35560067 | 2022 | Acquired spherocytosis due to somatic ANK1 mutations as a manifestation of clonal hematopoiesis in elderly patients. | 0 |
| 35631165 | 2022 | The SNP rs516946 Interacted in the Association of MetS with Dietary Iron among Chinese Males but Not Females. | 2 |
| 35560067 | 2022 | Acquired spherocytosis due to somatic ANK1 mutations as a manifestation of clonal hematopoiesis in elderly patients. | 0 |
| 35631165 | 2022 | The SNP rs516946 Interacted in the Association of MetS with Dietary Iron among Chinese Males but Not Females. | 2 |
| 33620149 | 2021 | Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis. | 10 |
Citation
Dessen P
ANK1 (ankyrin 1)
Atlas Genet Cytogenet Oncol Haematol. 2003-11-01
Online version: http://atlasgeneticsoncology.org/gene/641/ank1
