Variant ID | 8452 |
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Entrez Gene ID | 353376 |
Gene | TICAM2 (GeneCards) |
Location | hg19 5:114932318-114932318
hg38 5:115596621-115596621 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000005.9:g.114932318 C>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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.5726 |
CADD Raw score (version 1.3) | -0.213266 (Deleterious) |
FATHMM raw prediction score | 0.05661 (Tolerated) |
Deleterious probability by DeFine | 0.0793 (Neutral) |
Entrez Gene ID | 353376 (NCBI Gene) |
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Official Gene Symbol | TICAM2 (GeneCards) |
Number of variants in TICAM2 in this database | 2 (view all the variants) |
Full name | toll like receptor adaptor molecule 2 |
Band | 5q22.3 |
Other IDs | Vega: OTTHUMG00000162905 OMIM: 608321 HGNC: HGNC:21354 Ensembl: ENSG00000243414 |
Other names | TIRP, TRAM, TIRAP3, MyD88-4, TICAM-2 |
Summary | TIRP is a Toll/interleukin-1 receptor (IL1R; MIM 147810) (TIR) domain-containing adaptor protein involved in Toll receptor signaling (see TLR4; MIM 603030).[supplied by OMIM, Apr 2004] |
Individual ID | 29217584.15 (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; |