Overview

Variant ID 1596
Entrez Gene ID 1491
Gene CTH (GeneCards)
Location hg19 1:70966469-70966469
hg38 1:70500786-70500786
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000001.10:g.70966469 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 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.1243
CADD Raw score (version 1.3) -0.103639 (Deleterious)
FATHMM raw prediction score 0.16704 (Tolerated)
Deleterious probability by DeFine 0.1719 (Neutral)
Entrez Gene ID 1491 (NCBI Gene)
Official Gene Symbol CTH (GeneCards)
Number of variants in CTH in this database 4 (view all the variants)
Full name cystathionine gamma-lyase
Band 1p31.1
Other IDs Vega: OTTHUMG00000009352
OMIM: 607657
HGNC: HGNC:2501
Ensembl: ENSG00000116761
Other names None
Summary This gene encodes a cytoplasmic enzyme in the trans-sulfuration pathway that converts cystathione derived from methionine into cysteine. Glutathione synthesis in the liver is dependent upon the availability of cysteine. Mutations in this gene cause cystathioninuria. Alternative splicing of this gene results in three transcript variants encoding different isoforms. [provided by RefSeq, Jun 2010]

Individual #1

Individual ID 29217584.01 (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;