Identity
HGNC
LOCATION
17p13.1
LOCUSID
ALIAS
DNAHC2,DNHD3,SPGF45
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: 146754
MIM: 603333
HGNC: 2948
Ensembl: ENSG00000183914
Variants:
dbSNP: 146754
ClinVar: 146754
TCGA: ENSG00000183914
COSMIC: DNAH2
RNA/Proteins
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Huntington's disease | KEGG | ko05016 |
| Huntington's disease | KEGG | hsa05016 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33771466 | 2021 | Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella. | 11 |
| 33771466 | 2021 | Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella. | 11 |
| 30811583 | 2019 | DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella. | 37 |
| 30811583 | 2019 | DNAH2 is a novel candidate gene associated with multiple morphological abnormalities of the sperm flagella. | 37 |
Citation
Dessen P
DNAH2 (dynein axonemal heavy chain 2)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62550/dnah2-(dynein-axonemal-heavy-chain-2)
