Variant ID | 25244 |
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Entrez Gene ID | 89857 |
Gene | KLHL6 (GeneCards) |
Location | hg19 3:183351767-183351767
hg38 3:183633979-183633979 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000003.11:g.183351767 C>G (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 | 198022430 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.295 |
CADD Raw score (version 1.3) | -0.09312 (Deleterious) |
FATHMM raw prediction score | 0.07466 (Tolerated) |
Deleterious probability by DeFine | 0.2218 (Neutral) |
Entrez Gene ID | 89857 (NCBI Gene) |
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Official Gene Symbol | KLHL6 (GeneCards) |
Number of variants in KLHL6 in this database | 8 (view all the variants) |
Full name | kelch like family member 6 |
Band | 3q27.1 |
Other IDs | Vega: OTTHUMG00000148673 OMIM: 614214 HGNC: HGNC:18653 Ensembl: ENSG00000172578 |
Other names | None |
Summary | This gene encodes a member of the kelch-like (KLHL) family of proteins, which is involved in B-lymphocyte antigen receptor signaling and germinal-center B-cell maturation. The encoded protein contains an N-terminal broad-complex, tramtrack and bric a brac (BTB) domain that facilitates protein binding and dimerization, a BTB and C-terminal kelch (BACK) domain, and six C-terminal kelch repeat domains. Naturally occurring mutations in this gene are associated with chronic lymphocytic leukemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017] |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |