Overview

Variant ID 26104
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)

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 0.138
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)
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 #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