The DLX5 gene homepage

General information
Gene symbol DLX5
Gene name distal-less homeobox 5
Chromosome 7
Chromosomal band q21.3
Imprinted Unknown
Genomic reference NG_009220.1
Transcript reference NM_005221.5
Exon/intron information NM_005221.5 exon/intron table
Associated with diseases SHFM1, SHFM1D
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 9
Unique public DNA variants reported 9
Individuals with public variants 3
Hidden variants 1
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 July 07, 2023
Version DLX5:230707

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_005221.5.
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/DLX5
HGNC 2918
Entrez Gene 1749
PubMed articles DLX5
OMIM - Gene 600028
OMIM - Diseases SHFM1 (Split-hand/foot malformation 1)
SHFM1D (split-hand/foot malformation, type 1 with sensorineural hearing loss (SHFM-1D))
HGMD DLX5
GeneCards DLX5
GeneTests DLX5
Orphanet DLX5


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00006487 7 distal-less homeobox 5 NM_005221.5 NP_005212.1 9


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