Variant ID | 23121 |
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Entrez Gene ID | 9444 |
Gene | QKI (GeneCards) |
Location | hg19 6:164394058-164394058
hg38 6:163973026-163973026 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000006.11:g.164394058 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 | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0.0011 |
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EIGEN score | -0.6029 |
CADD Raw score (version 1.3) | -0.6746 (Deleterious) |
FATHMM raw prediction score | 0.08817 (Tolerated) |
Deleterious probability by DeFine | 0.3324 (Neutral) |
Entrez Gene ID | 9444 (NCBI Gene) |
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Official Gene Symbol | QKI (GeneCards) |
Number of variants in QKI in this database | 29 (view all the variants) |
Full name | QKI, KH domain containing RNA binding |
Band | 6q26 |
Other IDs | Vega: OTTHUMG00000015977 OMIM: 609590 HGNC: HGNC:21100 Ensembl: ENSG00000112531 |
Other names | QK, Hqk, QK1, QK3, hqkI |
Summary | The protein encoded by this gene is an RNA-binding protein that regulates pre-mRNA splicing, export of mRNAs from the nucleus, protein translation, and mRNA stability. The encoded protein is involved in myelinization and oligodendrocyte differentiation and may play a role in schizophrenia. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014] |
Individual ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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Title | Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis. |
Journal | Science |
Publication date | 2018.02 |
Disease | Asymptomatic |
Number of cases | cases of unknown sex: 3; |