Overview

Variant ID 10016
Entrez Gene ID 8521
Gene GCM1 (GeneCards)
Location hg19 6:53102075-53102075
hg38 6:53237277-53237277
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000006.11:g.53102075 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 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1042
CADD Raw score (version 1.3) 0.271679 (Deleterious)
FATHMM raw prediction score 0.13333 (Tolerated)
Deleterious probability by DeFine 0.4161 (Neutral)
Entrez Gene ID 8521 (NCBI Gene)
Official Gene Symbol GCM1 (GeneCards)
Number of variants in GCM1 in this database 4 (view all the variants)
Full name glial cells missing homolog 1
Band 6p12.1
Other IDs Vega: OTTHUMG00000014871
OMIM: 603715
HGNC: HGNC:4197
Ensembl: ENSG00000137270
Other names GCMA, hGCMa
Summary This gene encodes a DNA-binding protein with a gcm-motif (glial cell missing motif). The encoded protein is a homolog of the Drosophila glial cells missing gene (gcm). This protein binds to the GCM-motif (A/G)CCCGCAT, a novel sequence among known targets of DNA-binding proteins. The N-terminal DNA-binding domain confers the unique DNA-binding activity of this protein. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.15 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;