Variant ID | 24337 |
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Entrez Gene ID | 81849 |
Gene | ST6GALNAC5 (GeneCards) |
Location | hg19 1:77519893-77519893
hg38 1:77054208-77054208 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000001.10:g.77519893 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 | 249250621 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.1781 |
CADD Raw score (version 1.3) | 0.302244 (Deleterious) |
FATHMM raw prediction score | 0.19646 (Tolerated) |
Deleterious probability by DeFine | 0.5948 (Deleterious) |
Entrez Gene ID | 81849 (NCBI Gene) |
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Official Gene Symbol | ST6GALNAC5 (GeneCards) |
Number of variants in ST6GALNAC5 in this database | 3 (view all the variants) |
Full name | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 |
Band | 1p31.1 |
Other IDs | Vega: OTTHUMG00000009687 OMIM: 610134 HGNC: HGNC:19342 Ensembl: ENSG00000117069 |
Other names | SIAT7E, SIAT7-E, ST6GalNAcV |
Summary | The protein encoded by this gene is a Golgi type II transmembrane glycosyltransferase. The encoded protein catalyzes the transfer of sialic acid to cell surface proteins to modulate cell-cell interactions. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016] |
Individual ID | 29217587.02 (view all the variants in this individual) |
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Pubmed ID | 29217587 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Asymptomatic |
OMIM ID |