Variant ID | 34323 |
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Entrez Gene ID | 8997 |
Gene | KALRN (GeneCards) |
Location | hg19 3:124243596-124243596
hg38 3:124524749-124524749 |
Disease | Asymptomatic |
Method | Whole Genome Sequencing Ion Torrent PGM Sequencing |
Mutation(HGVS format) | NC_000003.11:g.124243596 T>C (Genome Assembly: hg19) |
Exon or Intron | intron |
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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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.1471 |
CADD Raw score (version 1.3) | -0.333728 (Deleterious) |
FATHMM raw prediction score | 0.1602 (Tolerated) |
Deleterious probability by DeFine | 0.4564 (Neutral) |
Entrez Gene ID | 8997 (NCBI Gene) |
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Official Gene Symbol | KALRN (GeneCards) |
Number of variants in KALRN in this database | 9 (view all the variants) |
Full name | kalirin RhoGEF kinase |
Band | 3q21.1-q21.2 |
Other IDs | Vega: OTTHUMG00000125545 OMIM: 604605 HGNC: HGNC:4814 Ensembl: ENSG00000160145 |
Other names | DUO, CHD5, DUET, TRAD, CHDS5, HAPIP, ARHGEF24 |
Summary | Huntington's disease (HD), a neurodegenerative disorder characterized by loss of striatal neurons, is caused by an expansion of a polyglutamine tract in the HD protein huntingtin. This gene encodes a protein that interacts with the huntingtin-associated protein 1, which is a huntingtin binding protein that may function in vesicle trafficking. [provided by RefSeq, Apr 2016] |
Individual ID | 24760347.01 (view all the variants in this individual) |
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Pubmed ID | 24760347 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 24760347 |
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Title | Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis |
Journal | Genome Research |
Publication date | 2014.04 |
Disease | Asymptomatic |
Number of cases | Female cases: 1; |