Variant ID | 26104 |
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Entrez Gene ID | 4121 |
Gene | MAN1A1 (GeneCards) |
Location | hg19 6:119757404-119757404
hg38 6:119436239-119436239 |
Disease | Asymptomatic |
Method | Single cell Sequencing Cell cloning |
Mutation(HGVS format) | NC_000006.11:g.119757404 G>T (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 | 171115067 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.138 |
CADD Raw score (version 1.3) | -0.102276 (Deleterious) |
FATHMM raw prediction score | 0.16985 (Tolerated) |
Deleterious probability by DeFine | 0.3282 (Neutral) |
Entrez Gene ID | 4121 (NCBI Gene) |
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Official Gene Symbol | MAN1A1 (GeneCards) |
Number of variants in MAN1A1 in this database | 4 (view all the variants) |
Full name | mannosidase alpha class 1A member 1 |
Band | 6q22.31 |
Other IDs | Vega: OTTHUMG00000015472 OMIM: 604344 HGNC: HGNC:6821 Ensembl: ENSG00000111885 |
Other names | MAN9, HUMM3, HUMM9 |
Summary | This gene encodes a class I mammalian Golgi 1,2-mannosidase which is a type II transmembrane protein. This protein catalyzes the hydrolysis of three terminal mannose residues from peptide-bound Man(9)-GlcNAc(2) oligosaccharides and belongs to family 47 of glycosyl hydrolases. [provided by RefSeq, Jul 2012] |
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 |