Overview

Variant ID 26073
Entrez Gene ID 10690
Gene FUT9 (GeneCards)
Location hg19 6:96538446-96538446
hg38 6:96090570-96090570
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000006.11:g.96538446 G>T (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 171115067

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3276
CADD Raw score (version 1.3) -0.074986 (Deleterious)
FATHMM raw prediction score 0.0547 (Tolerated)
Deleterious probability by DeFine 0.1806 (Neutral)
Entrez Gene ID 10690 (NCBI Gene)
Official Gene Symbol FUT9 (GeneCards)
Number of variants in FUT9 in this database 4 (view all the variants)
Full name fucosyltransferase 9
Band 6q16.1
Other IDs Vega: OTTHUMG00000015236
OMIM: 606865
HGNC: HGNC:4020
Ensembl: ENSG00000172461
Other names Fc-TIX
Summary The protein encoded by this gene belongs to the glycosyltransferase family. It is localized to the golgi, and catalyzes the last step in the biosynthesis of Lewis X (LeX) antigen, the addition of a fucose to precursor polysaccharides. This protein is one of the few fucosyltransferases that synthesizes the LeX oligosaccharide (CD15) expressed in the organ buds progressing in mesenchyma during embryogenesis. It is also responsible for the expression of CD15 in mature granulocytes. A common haplotype of this gene has also been associated with susceptibility to placental malaria infection. [provided by RefSeq, Nov 2011]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID