Overview

Variant ID 12942
Entrez Gene ID 23081
Gene KDM4C (GeneCards)
Location hg19 9:6937827-6937827
hg38 9:6937827-6937827
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000009.11:g.6937827 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 141213431

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.4753
CADD Raw score (version 1.3) -0.167458 (Deleterious)
FATHMM raw prediction score 0.05836 (Tolerated)
Deleterious probability by DeFine 0.1283 (Neutral)
Entrez Gene ID 23081 (NCBI Gene)
Official Gene Symbol KDM4C (GeneCards)
Number of variants in KDM4C in this database 16 (view all the variants)
Full name lysine demethylase 4C
Band 9p24.1
Other IDs Vega: OTTHUMG00000187508
OMIM: 605469
HGNC: HGNC:17071
Ensembl: ENSG00000107077
Other names GASC1, JHDM3C, JMJD2C, TDRD14C
Summary This gene is a member of the Jumonji domain 2 (JMJD2) family. The encoded protein is a trimethylation-specific demethylase, and converts specific trimethylated histone residues to the dimethylated form. This enzymatic action regulates gene expression and chromosome segregation. Chromosomal aberrations and changes in expression of this gene may be found in tumor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

Individual #1

Individual ID 29217584.03 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;