Overview

Variant ID 3734
Entrez Gene ID 79809
Gene TTC21B (GeneCards)
Location hg19 2:166735175-166735175
hg38 2:165878665-165878665
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000002.11:g.166735175 A>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 243199373

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.5305
CADD Raw score (version 1.3) 1.112042 (Deleterious)
FATHMM raw prediction score 0.83944 (Tolerated)
Deleterious probability by DeFine 0.3959 (Neutral)
Entrez Gene ID 79809 (NCBI Gene)
Official Gene Symbol TTC21B (GeneCards)
Number of variants in TTC21B in this database 4 (view all the variants)
Full name tetratricopeptide repeat domain 21B
Band 2q24.3
Other IDs Vega: OTTHUMG00000154083
OMIM: 612014
HGNC: HGNC:25660
Ensembl: ENSG00000123607
Other names ATD4, THM1, SRTD4, IFT139, JBTS11, NPHP12, IFT139B, Nbla10696
Summary This gene encodes a member of TTC21 family, containing several tetratricopeptide repeat (TPR) domains. This protein is localized to the cilium axoneme, and may play a role in retrograde intraflagellar transport in cilia. Mutations in this gene are associated with various ciliopathies, nephronophthisis 12, and asphyxiating thoracic dystrophy 4. [provided by RefSeq, Oct 2011]

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;