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: 26153
MIM: 613231
HGNC: 20226
Ensembl: ENSG00000066735
Variants:
dbSNP: 26153
ClinVar: 26153
TCGA: ENSG00000066735
COSMIC: KIF26A
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000066735 | ENST00000315264 | C9JFF0 |
| ENSG00000066735 | ENST00000423312 | Q9ULI4 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36564622 | 2023 | KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon. | 0 |
| 36564622 | 2023 | KIF26A is mutated in the syndrome of congenital hydrocephalus with megacolon. | 0 |
| 36228617 | 2022 | Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis. | 4 |
| 36228617 | 2022 | Loss of non-motor kinesin KIF26A causes congenital brain malformations via dysregulated neuronal migration and axonal growth as well as apoptosis. | 4 |
Citation
Dessen P
KIF26A (kinesin family member 26A)
Atlas Genet Cytogenet Oncol Haematol. 2014-08-01
Online version: http://atlasgeneticsoncology.org/gene/54413/kif26a-(kinesin-family-member-26a)
