Dynein axonemal heavy chain 5 (Q21114318)

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mammalian protein found in Homo sapiens
  • dynein heavy chain 5, axonemal
  • DNAH5
  • axonemal beta dynein heavy chain 5
  • ciliary dynein heavy chain 5
  • dynein, axonemal, heavy polypeptide 5
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Language Label Description Also known as
English
Dynein axonemal heavy chain 5
mammalian protein found in Homo sapiens
  • dynein heavy chain 5, axonemal
  • DNAH5
  • axonemal beta dynein heavy chain 5
  • ciliary dynein heavy chain 5
  • dynein, axonemal, heavy polypeptide 5

Statements

molecular function
cell component
axoneme
determination method
IDA
7 references
retrieved
27 March 2018
stated in
Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm.
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
27 March 2018
stated in
Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
27 March 2018
stated in
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
27 March 2018
stated in
Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
27 March 2018
stated in
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry
GOA
curator
Mouse Genome Informatics
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
27 March 2018
stated in
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex
GOA
curator
Mouse Genome Informatics
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
27 March 2018
stated in
DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes
GOA
curator
GO Central
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IDA
axoneme
determination method
IDA
IEA
8 references
retrieved
9 May 2019
stated in
GOA
curator
Ensembl genome database project
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IEA
retrieved
9 May 2019
stated in
Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
9 May 2019
stated in
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
9 May 2019
stated in
Axonemal localization of the dynein component DNAH5 is not altered in secondary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
9 May 2019
stated in
Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm.
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
9 May 2019
stated in
ARMC4 mutations cause primary ciliary dyskinesia with randomization of left/right body asymmetry
GOA
curator
Mouse Genome Informatics
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
9 May 2019
stated in
Loss-of-Function GAS8 Mutations Cause Primary Ciliary Dyskinesia and Disrupt the Nexin-Dynein Regulatory Complex
GOA
curator
Mouse Genome Informatics
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
retrieved
9 May 2019
stated in
DNAH11 Localization in the Proximal Region of Respiratory Cilia Defines Distinct Outer Dynein Arm Complexes
GOA
curator
GO Central
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IDA
biological process
outer dynein arm assembly
determination method
IMP
7 references
retrieved
27 March 2018
stated in
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
27 March 2018
stated in
Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
27 March 2018
stated in
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
27 March 2018
stated in
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
27 March 2018
stated in
High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
27 March 2018
stated in
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
27 March 2018
stated in
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?protein=Q8TE73&geneProductId=UniProtKB:Q8TE73
determination method
IMP
outer dynein arm assembly
determination method
IBA
IMP
8 references
retrieved
9 May 2019
stated in
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia
GOA
curator
Syscilia
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IMP
retrieved
9 May 2019
stated in
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
GOA
curator
GO Central
reference URL
http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q8TE73
determination method
IBA

Identifiers

 
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