The DNAH1 gene homepage

General information
Gene symbol DNAH1
Gene name dynein, axonemal, heavy chain 1
Chromosome 3
Chromosomal band p21-p14
Imprinted Unknown
Genomic reference NG_052911.1
Transcript reference NM_015512.4
Exon/intron information NM_015512.4 exon/intron table
Associated with diseases CILD, CILD37, SPGF, SPGF18
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 141
Unique public DNA variants reported 114
Individuals with public variants 197
Hidden variants 12
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created May 03, 2013
Date last updated April 22, 2024
Version DNAH1:240422

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_015512.4.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/DNAH1
HGNC 2940
Entrez Gene 25981
PubMed articles DNAH1
OMIM - Gene 603332
OMIM - Diseases CILD37 (dyskinesia, ciliary, primary, type 37 (CILD37))
SPGF18 (spermatogenic failure, type 18 (SPGF18))
HGMD DNAH1
GeneCards DNAH1
GeneTests DNAH1
Orphanet DNAH1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006516 3 dynein, axonemal, heavy chain 1 NM_015512.4 NP_056327.4 141


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