Overview

Variant ID 7519
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)

Other information

Exon or Intron NA
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

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
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)
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 #1

Individual ID 29217584.03 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
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;