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Gene: ALG9 (ALG9 alpha-1,2-mannosyltransferase) Homo sapiens
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Symbol: ALG9
Name: ALG9 alpha-1,2-mannosyltransferase
Description: Predicted to have mannosyltransferase activity. Predicted to be involved in dolichol-linked oligosaccharide biosynthetic process. Localizes to the membrane. Implicated in congenital disorder of glycosylation Il.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: ALG9, alpha-1,2-mannosyltransferase; alpha-1,2-mannosyltransferase ALG9; asparagine-linked glycosylation 9 homolog (S. cerevisiae, alpha- 1,2-mannosyltransferase); asparagine-linked glycosylation 9 homolog (yeast, alpha 1,2 mannosyltransferase); asparagine-linked glycosylation 9 homolog (yeast, alpha- 1,2-mannosyltransferase); asparagine-linked glycosylation 9, alpha-1,2-mannosyltransferase homolog; asparagine-linked glycosylation protein 9 homolog; CDG1L; DIBD1; disrupted in bipolar affective disorder 1; disrupted in bipolar disorder protein 1; DKFZp586M2420; dol-P-Man dependent alpha-1,2-mannosyltransferase; dol-P-Man:Man(6)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase; dol-P-Man:Man(8)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase; dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase; dolichyl-P-Man:Man(8)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase; FLJ21845; GIKANIS; LOH11CR1J; loss of heterozygosity, 11, chromosomal region 1 gene J product
Orthologs:
Mus musculus (house mouse) : Alg9 (asparagine-linked glycosylation 9 (alpha 1,2 mannosyltransferase))  MGI  Alliance
Rattus norvegicus (Norway rat) : Alg9 (ALG9, alpha-1,2-mannosyltransferase)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Alg9 (ALG9 alpha-1,2-mannosyltransferase)
Pan paniscus (bonobo/pygmy chimpanzee) : ALG9 (ALG9 alpha-1,2-mannosyltransferase)
Canis lupus familiaris (dog) : ALG9 (ALG9 alpha-1,2-mannosyltransferase)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Alg9 (ALG9 alpha-1,2-mannosyltransferase)
Sus scrofa (pig) : ALG9 (ALG9 alpha-1,2-mannosyltransferase)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh3811111,776,096 - 111,871,581 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3711111,652,919 - 111,742,305 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 3611111,158,129 - 111,247,515 (-)NCBINCBI36hg18NCBI36
Build 3411111,162,218 - 111,247,515NCBI
Celera11108,806,108 - 108,895,523 (-)NCBI
Cytogenetic Map11q23.1NCBI
HuRef11107,576,803 - 107,666,274 (-)NCBIHuRef
CHM1_111111,535,968 - 111,625,360 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
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References - curated
References - uncurated

Genomics

Comparative Map Data
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miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
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Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on ALG9
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1342764
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-10-16
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.