Overview

Variant ID 25244
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)

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 198022430

Annotations and predictions

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

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID