ENSG00000090581


Homo sapiens

Features
Gene ID: ENSG00000090581
  
Biological name :GNPTG
  
Synonyms : GNPTG / N-acetylglucosamine-1-phosphate transferase gamma subunit / Q9UJJ9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 16
Strand: 1
Band: p13.3
Gene start: 1351923
Gene end: 1364113
  
Corresponding Affymetrix probe sets: 224887_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000435349
Ensembl peptide - ENSP00000480060
Ensembl peptide - ENSP00000460728
Ensembl peptide - ENSP00000204679
Ensembl peptide - ENSP00000434413
NCBI entrez gene - 84572     See in Manteia.
OMIM - 607838
RefSeq - NM_032520
RefSeq - XM_017023783
RefSeq - XM_017023782
RefSeq Peptide - NP_115909
swissprot - E9PQQ5
swissprot - Q9UJJ9
swissprot - H0YEA7
swissprot - A0A087WWA2
Ensembl - ENSG00000090581
  
Related genetic diseases (OMIM): 252605 - Mucolipidosis III gamma, 252605
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 gnptgENSDARG00000038566Danio rerio
 GNPTGENSGALG00000006441Gallus gallus
 GnptgENSMUSG00000035521Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR009011  Mannose-6-phosphate receptor binding domain superfamily
 IPR010506  DMAP1-binding domain
 IPR012913  Protein OS9-like
 IPR036607  Glucosidase 2 subunit beta-like


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0016256 N-glycan processing to lysosome IEA
 biological_processGO:0046835 carbohydrate phosphorylation IDA
 cellular_componentGO:0000139 Golgi membrane IEA
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005794 Golgi apparatus ISS
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 molecular_functionGO:0003976 UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase activity IEA
 molecular_functionGO:0042803 protein homodimerization activity ISS


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000280 Coarse facial features 
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 HP:0000470 Short neck 
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 HP:0000545 Myopia 
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 HP:0000768 Pectus carinatum "A deformity of the chest caused by overgrowth of the ribs and characterized by protrusion of the sternum." [HPO:curators]
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 HP:0000943 Dysostosis multiplex 
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 HP:0001155 Abnormality of the hand "An abnormality affecting one or both hands." [HPO:curators]
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 HP:0001256 Mental retardation, mild "Mild mental retardation is defined as an intelligence quotient (IQ) in the range of 50-69." [HPO:curators]
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 HP:0001387 Joint stiffness "Joint stiffness is a perceived sensation of tightness in a joint or joints when attempting to move them after a period of inactivity. Joint stiffness typically subsides over time." [HPO:curators]
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 HP:0001547 Abnormality of the morphology or size of the rib cage 
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 HP:0001650 Aortic stenosis "The presence of a stenosis (narrowing) of the aortic valve." [HPO:curators]
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 HP:0001659 Aortic insufficiency "An insufficiency of the aortic valve, leading to regurgitation (backward flow) of blood from the aorta into the left ventricle." [HPO:curators]
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0002808 Kyphosis 
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 HP:0002829 Arthralgia 
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 HP:0002857 Genu valgum 
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 HP:0002869 Flared iliac wings 
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 HP:0003307 Hyperlordosis 
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 HP:0003333 Increased serum beta-hexosaminidase (10-20x) 
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 HP:0003370 Flat capital femoral epiphyses 
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 HP:0003538 Increased serum iduronate sulfatase (10-20x) 
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0007759 Corneal opacities, not impairing visual acuity 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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