The HOXC13 gene homepage

General information
Gene symbol HOXC13
Gene name homeobox C13
Chromosome 12
Chromosomal band q13.13
Imprinted Unknown
Genomic reference NC_000012.11
Transcript reference NM_017410.2
Exon/intron information NM_017410.2 exon/intron table
Associated with diseases ECTD9
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 6
Unique public DNA variants reported 6
Individuals with public variants 1
Hidden variants 1
Date created December 05, 2012
Date last updated April 19, 2024
Version HOXC13:240419

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_017410.2.
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
HGNC 5125
Entrez Gene 3229
PubMed articles HOXC13
OMIM - Gene 142976
OMIM - Diseases ECTD9 (dysplasia, ectodermal, type 9, hair/nail (ECTD-9))
HGMD HOXC13
GeneCards HOXC13
GeneTests HOXC13
Orphanet HOXC13


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00001770 12 homeobox C13 NM_017410.2 NP_059106.2 6


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