Variant ID | 2642 |
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Entrez Gene ID | 256435 |
Gene | ST6GALNAC3 (GeneCards) |
Location | hg19 1:77146121-77146121
hg38 1:76680436-76680436 |
Disease | Cockayne syndrome (view all the variants in this disease) |
Method | HiSeq X Ten |
Mutation(HGVS format) | NC_000001.10:g.77146121 C>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 | 249250621 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | -0.0968 |
CADD Raw score (version 1.3) | -0.039997 (Deleterious) |
FATHMM raw prediction score | 0.12408 (Tolerated) |
Deleterious probability by DeFine | 0.7008 (Deleterious) |
Entrez Gene ID | 256435 (NCBI Gene) |
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Official Gene Symbol | ST6GALNAC3 (GeneCards) |
Number of variants in ST6GALNAC3 in this database | 8 (view all the variants) |
Full name | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 |
Band | 1p31.1 |
Other IDs | Vega: OTTHUMG00000009615 OMIM: 610133 HGNC: HGNC:19343 Ensembl: ENSG00000184005 |
Other names | STY, SIAT7C, PRO7177, ST6GALNACIII |
Summary | ST6GALNAC3 belongs to a family of sialyltransferases that transfer sialic acids from CMP-sialic acid to terminal positions of carbohydrate groups in glycoproteins and glycolipids (Lee et al., 1999 [PubMed 10207017]).[supplied by OMIM, Mar 2008] |
Individual ID | 29217584.17 (view all the variants in this individual) |
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Pubmed ID | 29217584 |
Whose mosaic mutation | Female Patient |
Phenotype | 3 |
Disease | Cockayne syndrome (view all the variants in this disease) |
OMIM ID | 216400 |
Pubmed ID | 29217584 |
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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; |