The CHCHD10 gene homepage

General information
Gene symbol CHCHD10
Gene name coiled-coil-helix-coiled-coil-helix domain containing 10
Chromosome 22
Chromosomal band q11.23
Imprinted Unknown
Genomic reference NC_000022.10
Transcript reference NM_213720.1
Associated with diseases FTDALS-2, IMMD, SMAJ
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 28
Unique public DNA variants reported 18
Individuals with public variants 1
Hidden variants 3
Date created May 03, 2013
Date last updated September 17, 2021
Version CHCHD10:210917

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
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 15559
Entrez Gene 400916
PubMed articles CHCHD10
OMIM - Gene 615903
OMIM - Diseases FTDALS-2 (dementia, frontotemporal, and/or amyotrophic lateral sclerosis, type 2 (FTDALS-2))
IMMD (myopathy?, isolated mitochondrial, autosomal dominant(IMMD))
SMAJ (atrophy, muscular, spinal, Jokela type (SMAJ))
Orphanet CHCHD10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00005076 22 coiled-coil-helix-coiled-coil-helix domain containing 10 NM_213720.1 NP_998885.1 28


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