Overview

Variant ID 6881
Entrez Gene ID 2638
Gene GC (GeneCards)
Location hg19 4:72618403-72618403
hg38 4:71752686-71752686
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000004.11:g.72618403 G>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 191154276

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.2359
CADD Raw score (version 1.3) -0.175746 (Deleterious)
FATHMM raw prediction score 0.14374 (Tolerated)
Deleterious probability by DeFine 0.7356 (Deleterious)
Entrez Gene ID 2638 (NCBI Gene)
Official Gene Symbol GC (GeneCards)
Number of variants in GC in this database 6 (view all the variants)
Full name GC, vitamin D binding protein
Band 4q13.3
Other IDs Vega: OTTHUMG00000129915
OMIM: 139200
HGNC: HGNC:4187
Ensembl: ENSG00000145321
Other names DBP, VDB, GRD3, VDBG, VDBP, GcMAF, DBP/GC, Gc-MAF, DBP-maf, HEL-S-51
Summary The protein encoded by this gene belongs to the albumin gene family. It is a multifunctional protein found in plasma, ascitic fluid, cerebrospinal fluid and on the surface of many cell types. It binds to vitamin D and its plasma metabolites and transports them to target tissues. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2011]

Individual #1

Individual ID 29217584.13 (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;