Variant ID | 3734 |
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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) |
Exon or Intron | NA |
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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 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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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) |
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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 ID | 29217584.11 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217584 |
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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; |