Variant ID | 7519 |
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Entrez Gene ID | 51194 |
Gene | IPO11 (GeneCards) |
Location | hg19 5:62101341-62101341
hg38 5:62805514-62805514 |
Disease | Asymptomatic |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000005.9:g.62101341 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 | -0.3386 |
CADD Raw score (version 1.3) | -0.026541 (Deleterious) |
FATHMM raw prediction score | 0.07132 (Tolerated) |
Deleterious probability by DeFine | 0.0888 (Neutral) |
Entrez Gene ID | 51194 (NCBI Gene) |
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Official Gene Symbol | IPO11 (GeneCards) |
Number of variants in IPO11 in this database | 12 (view all the variants) |
Full name | importin 11 |
Band | 5q12.1 |
Other IDs | Vega: OTTHUMG00000154400 OMIM: 610889 HGNC: HGNC:20628 Ensembl: ENSG00000086200 |
Other names | RanBP11 |
Summary | Importins, including IPO11, are a members of the karyopherin/importin-beta family of transport receptors (see KPNB1; 602738) that mediate nucleocytoplasmic transport of protein and RNA cargoes (Plafker and Macara, 2000 [PubMed 11032817]).[supplied by OMIM, Sep 2008] |
Individual ID | 29217584.03 (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; |