Identity
HGNC
LOCATION
11p15.4
LOCUSID
ALIAS
C11orf47,CCDC35,DHCD1,DNHD1L
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: 144132
MIM: 617277
HGNC: 26532
Ensembl: ENSG00000179532
Variants:
dbSNP: 144132
ClinVar: 144132
TCGA: ENSG00000179532
COSMIC: DNHD1
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36768883 | 2023 | New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. | 2 |
| 36768883 | 2023 | New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella. | 2 |
| 34932939 | 2022 | Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. | 14 |
| 34932939 | 2022 | Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice. | 14 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
| 20379614 | 2010 | Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score. | 78 |
Citation
Dessen P
DNHD1 (dynein heavy chain domain 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62577/dnhd1-(dynein-heavy-chain-domain-1)
