Overview

Variant ID 12205
Entrez Gene ID 57623
Gene ZFAT (GeneCards)
Location hg19 8:135802652-135802652
hg38 8:134790409-134790409
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000008.10:g.135802652 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 146364022

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2132
CADD Raw score (version 1.3) 0.545963 (Deleterious)
FATHMM raw prediction score 0.1009 (Tolerated)
Deleterious probability by DeFine 0.3448 (Neutral)
Entrez Gene ID 57623 (NCBI Gene)
Official Gene Symbol ZFAT (GeneCards)
Number of variants in ZFAT in this database 6 (view all the variants)
Full name zinc finger and AT-hook domain containing
Band 8q24.22
Other IDs Vega: OTTHUMG00000164321
OMIM: 610931
HGNC: HGNC:19899
Ensembl: ENSG00000066827
Other names AITD3, ZFAT1, ZNF406
Summary This gene encodes a protein that likely binds DNA and functions as a transcriptional regulator involved in apoptosis and cell survival. This gene resides in a susceptibility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Nov 2009]

Individual #1

Individual ID 29217584.11 (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;