Overview

Variant ID 23386
Entrez Gene ID 157855
Gene KCNU1 (GeneCards)
Location hg19 8:36696527-36696527
hg38 8:36839009-36839009
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000008.10:g.36696527 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 146364022

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.2115
CADD Raw score (version 1.3) -0.189021 (Deleterious)
FATHMM raw prediction score 0.10224 (Tolerated)
Deleterious probability by DeFine 0.6911 (Deleterious)
Entrez Gene ID 157855 (NCBI Gene)
Official Gene Symbol KCNU1 (GeneCards)
Number of variants in KCNU1 in this database 5 (view all the variants)
Full name potassium calcium-activated channel subfamily U member 1
Band 8p11.23
Other IDs Vega: OTTHUMG00000163981
OMIM: 615215
HGNC: HGNC:18867
Ensembl: ENSG00000215262
Other names KCa5, Slo3, KCNMC1, KCa5.1, Kcnma3
Summary This gene encodes a member of the potassium channel family of proteins. The encoded voltage-gated ion channel allows the outward flow of potassium ions during plasma membrane hyperpolarization in sperm. Opening of this channel may be regulated by calcium ion levels. Homozygous knockout mice that lack the related mouse gene exhibit male sterility. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
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;