Overview

Variant ID 6901
Entrez Gene ID 166815
Gene TIGD2 (GeneCards)
Location hg19 4:90106797-90106797
hg38 4:89185646-89185646
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000004.11:g.90106797 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 191154276

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0.00006502
EIGEN score -0.8598
CADD Raw score (version 1.3) -0.765335 (Deleterious)
FATHMM raw prediction score 0.0291 (Tolerated)
Deleterious probability by DeFine 0.1119 (Neutral)
Entrez Gene ID 166815 (NCBI Gene)
Official Gene Symbol TIGD2 (GeneCards)
Number of variants in TIGD2 in this database 3 (view all the variants)
Full name tigger transposable element derived 2
Band 4q22.1
Other IDs Vega: OTTHUMG00000130946
OMIM: 612973
HGNC: HGNC:18333
Ensembl: ENSG00000180346
Other names HEL106
Summary The protein encoded by this gene belongs to the tigger subfamily of the pogo superfamily of DNA-mediated transposons in humans. These proteins are related to DNA transposons found in fungi and nematodes, and more distantly to the Tc1 and mariner transposases. They are also very similar to the major mammalian centromere protein B. The exact function of this gene is not known. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.13 (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;