The HMX1 gene homepage

General information
Gene symbol HMX1
Gene name H6 family homeobox 1
Chromosome 4
Chromosomal band p16.1
Imprinted Unknown
Genomic reference NG_013062.1
Transcript reference NM_018942.2
Exon/intron information NM_018942.2 exon/intron table
Associated with diseases OAS
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 38
Unique public DNA variants reported 36
Individuals with public variants 3
Hidden variants 1
Date created May 03, 2013
Date last updated April 19, 2024
Version HMX1:240419

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_018942.2.
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 http://www.LOVD.nl/HMX1
HGNC 5017
Entrez Gene 3166
PubMed articles HMX1
OMIM - Gene 142992
OMIM - Diseases OAS (oculo-auricular syndrome (OAS))
HGMD HMX1
GeneCards HMX1
GeneTests HMX1
Orphanet HMX1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00009491 4 H6 family homeobox 1 NM_018942.2 NP_061815.2 38


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