Identity
HGNC
LOCATION
17p12
LOCUSID
ALIAS
CILD40,DNAH17L,DNEL1,DYH9,Dnahc9,HL-20,HL20
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: 1770
MIM: 603330
HGNC: 2953
Ensembl: ENSG00000007174
Variants:
dbSNP: 1770
ClinVar: 1770
TCGA: ENSG00000007174
COSMIC: DNAH9
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 |
|---|---|---|---|
| 37486510 | 2024 | Meta-analysis of Transcriptomic Data from Lung Autopsy and Cellular Models of SARS-CoV-2 Infection. | 1 |
| 37486510 | 2024 | Meta-analysis of Transcriptomic Data from Lung Autopsy and Cellular Models of SARS-CoV-2 Infection. | 1 |
| 35050399 | 2022 | Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease. | 5 |
| 36140829 | 2022 | Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries. | 3 |
| 35050399 | 2022 | Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease. | 5 |
| 36140829 | 2022 | Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries. | 3 |
| 33610189 | 2021 | Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia. | 11 |
| 34008076 | 2021 | Whole-exome sequencing reveals a combination of extremely rare single-nucleotide polymorphism of DNAH9 and RSPH1 genes in a Japanese fetus with situs viscerum inversus. | 1 |
| 33610189 | 2021 | Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia. | 11 |
| 34008076 | 2021 | Whole-exome sequencing reveals a combination of extremely rare single-nucleotide polymorphism of DNAH9 and RSPH1 genes in a Japanese fetus with situs viscerum inversus. | 1 |
| 30471717 | 2018 | Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus. | 55 |
| 30471718 | 2018 | Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects. | 61 |
| 30471717 | 2018 | Mutations in Outer Dynein Arm Heavy Chain DNAH9 Cause Motile Cilia Defects and Situs Inversus. | 55 |
| 30471718 | 2018 | Recessive DNAH9 Loss-of-Function Mutations Cause Laterality Defects and Subtle Respiratory Ciliary-Beating Defects. | 61 |
| 26797031 | 2016 | Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsiveness. | 9 |
Citation
Dessen P
DNAH9 (dynein axonemal heavy chain 9)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/62556/dnah9-(dynein-axonemal-heavy-chain-9)
