Overview

Variant ID 6065
Entrez Gene ID 6870
Gene TACR3 (GeneCards)
Location hg19 4:104966751-104966751
hg38 4:104045594-104045594
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000004.11:g.104966751 C>G (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
EIGEN score -0.3551
CADD Raw score (version 1.3) -0.383867 (Deleterious)
FATHMM raw prediction score 0.07459 (Tolerated)
Deleterious probability by DeFine 0.4257 (Neutral)
Entrez Gene ID 6870 (NCBI Gene)
Official Gene Symbol TACR3 (GeneCards)
Number of variants in TACR3 in this database 11 (view all the variants)
Full name tachykinin receptor 3
Band 4q24
Other IDs Vega: OTTHUMG00000131124
OMIM: 162332
HGNC: HGNC:11528
Ensembl: ENSG00000169836
Other names NK3, NKR, HH11, NK3R, NK-3R, TAC3R, TAC3RL
Summary This gene belongs to a family of genes that function as receptors for tachykinins. Receptor affinities are specified by variations in the 5'-end of the sequence. The receptors belonging to this family are characterized by interactions with G proteins and 7 hydrophobic transmembrane regions. This gene encodes the receptor for the tachykinin neurokinin 3, also referred to as neurokinin B. [provided by RefSeq, Jul 2008]

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;