Variant ID | 22970 |
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Entrez Gene ID | 337876 |
Gene | CHSY3 (GeneCards) |
Location | hg19 5:130216443-130216443
hg38 5:130880750-130880750 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000005.9:g.130216443 G>A (Genome Assembly: GRCh37) |
Exon or Intron | NA |
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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 | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0.0009 |
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EIGEN score | 0.1507 |
CADD Raw score (version 1.3) | 0.952865 (Deleterious) |
FATHMM raw prediction score | 0.1125 (Tolerated) |
Deleterious probability by DeFine | 0.3421 (Neutral) |
Entrez Gene ID | 337876 (NCBI Gene) |
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Official Gene Symbol | CHSY3 (GeneCards) |
Number of variants in CHSY3 in this database | 12 (view all the variants) |
Full name | chondroitin sulfate synthase 3 |
Band | 5q23.3 |
Other IDs | Vega: OTTHUMG00000163043 OMIM: 609963 HGNC: HGNC:24293 Ensembl: ENSG00000198108 |
Other names | CSS3, CHSY2 |
Summary | CSS3 is a glycosyltransferase that has both glucuronyltransferase and N-acetylgalactosaminyltransferase activities (Yada et al., 2003 [PubMed 12907687]).[supplied by OMIM, Mar 2008] |
Individual ID | 29217587.01 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |
Pubmed ID | 29217587 |
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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; |