Overview

Variant ID 1640
Entrez Gene ID 55277
Gene FGGY (GeneCards)
Location hg19 1:59902198-59902198
hg38 1:59436526-59436526
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000001.10:g.59902198 G>A (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 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1352
CADD Raw score (version 1.3) -0.034515 (Deleterious)
FATHMM raw prediction score 0.12772 (Tolerated)
Deleterious probability by DeFine 0.5552 (Deleterious)
Entrez Gene ID 55277 (NCBI Gene)
Official Gene Symbol FGGY (GeneCards)
Number of variants in FGGY in this database 5 (view all the variants)
Full name FGGY carbohydrate kinase domain containing
Band 1p32.1
Other IDs Vega: OTTHUMG00000008424
OMIM: 611370
HGNC: HGNC:25610
Ensembl: ENSG00000172456
Other names None
Summary This gene encodes a protein that phosphorylates carbohydrates such as ribulose, ribitol, and L-arabinitol. Genome-wide association studies in some populations have found an association between polymorphisms in this gene and sporadic amyotrophic lateral sclerosis, but studies of other populations have not been able to replicate this association. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]

Individual #1

Individual ID 29217584.02 (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;