ALG9

GENE INFORMATION

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Gene name

ALG9 (HGNC Symbol)

Synonyms

DIBD1

Description

ALG9, alpha-1,2-mannosyltransferase (HGNC Symbol)

Entrez gene summary

This gene encodes an alpha-1,2-mannosyltransferase enzyme that functions in lipid-linked oligosaccharide assembly. Mutations in this gene result in congenital disorder of glycosylation type Il. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

Chromosome

11 (Chromosome progress)

Cytoband

q23.1

Chromosome location (bp)

111652919 - 111742305

Ensembl

ENSG00000086848 (version 73.37)

Entrez gene

79796

UniProt

Q9H6U8 (UniProt - Evidence at protein level)

neXtProt

NX_Q9H6U8

Antibodypedia

ALG9 antibodies
 

PROTEIN VIEW

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ALG9-010
 
ALG9-011
 
ALG9-017
 
ALG9-019
 
ALG9-020
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ALG9-010 ENSP00000381090
ENST00000398006
Q9H6U8
Show all »
Show » Show » 440 50.8 Yes 6
ALG9-011 ENSP00000435517
ENST00000531154
Q9H6U8
Show all »
Show » Show » 447 51.7 Yes 6
ALG9-017 ENSP00000432442
ENST00000532425
Show » 207 24.2 Yes 0
ALG9-019 ENSP00000437211
ENST00000525910
24 2.6 No 0
ALG9-020 ENSP00000436798
ENST00000524671
35 4 No 0