Variant ID | 3034 |
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Entrez Gene ID | 29851 |
Gene | ICOS (GeneCards) |
Location | hg19 2:205248150-205248150
hg38 2:204383427-204383427 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000002.11:g.205248150 G>A (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) | 0.00009705 |
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EIGEN score | -0.3105 |
CADD Raw score (version 1.3) | -0.012129 (Deleterious) |
FATHMM raw prediction score | 0.06943 (Tolerated) |
Deleterious probability by DeFine | 0.0577 (Neutral) |
Entrez Gene ID | 29851 (NCBI Gene) |
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Official Gene Symbol | ICOS (GeneCards) |
Number of variants in ICOS in this database | 5 (view all the variants) |
Full name | inducible T cell costimulator |
Band | 2q33.2 |
Other IDs | Vega: OTTHUMG00000132880 OMIM: 604558 HGNC: HGNC:5351 Ensembl: ENSG00000163600 |
Other names | AILIM, CD278, CVID1 |
Summary | The protein encoded by this gene belongs to the CD28 and CTLA-4 cell-surface receptor family. It forms homodimers and plays an important role in cell-cell signaling, immune responses, and regulation of cell proliferation. [provided by RefSeq, Jul 2008] |
Individual ID | 29217584.04 (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; |