Variant ID | 19004 |
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Entrez Gene ID | 663 |
Gene | BNIP2 (GeneCards) |
Location | hg19 15:60209803-60209803
hg38 15:59917604-59917604 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000015.9:g.60209803 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 | 102531392 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.2959 |
CADD Raw score (version 1.3) | 0.122155 (Deleterious) |
FATHMM raw prediction score | 0.26862 (Tolerated) |
Deleterious probability by DeFine | 0.8128 (Deleterious) |
Entrez Gene ID | 663 (NCBI Gene) |
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Official Gene Symbol | BNIP2 (GeneCards) |
Number of variants in BNIP2 in this database | 8 (view all the variants) |
Full name | BCL2 interacting protein 2 |
Band | 15q22.2 |
Other IDs | Vega: OTTHUMG00000132727 OMIM: 603292 HGNC: HGNC:1083 Ensembl: ENSG00000140299 |
Other names | NIP2, BNIP-2 |
Summary | This gene is a member of the BCL2/adenovirus E1B 19 kd-interacting protein (BNIP) family. It interacts with the E1B 19 kDa protein, which protects cells from virally-induced cell death. The encoded protein also interacts with E1B 19 kDa-like sequences of BCL2, another apoptotic protector. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
Individual ID | 29217584.10 (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; |