1. Gene
  2. OGT - O-linked N-acetylglucosamine (GlcNAc) transferase Gene

OGT - O-linked N-acetylglucosamine (GlcNAc) transferase Gene

Homo sapiens

Also known as OGT1; HRNT1; MRX106; XLID106; HINCUT-1; O-GLCNAC

Gene ID: 8473 | Gene type: protein coding

About OGT

Cytogenetic location: Xq13.1 Genomic coordinates (GRCh38): X:71,533,104-71,575,892 (from NCBI)

This gene has 21 transcripts (splice variants), 263 orthologues, 14 paralogues and is associated with 3 phenotypes. Ubiquitous expression in lymph node (RPKM 56.6), spleen (RPKM 53.1) and 25 other tissues.

Summary

This gene encodes a Glycosyltransferase that catalyzes the addition of a single N-acetylglucosamine in O-glycosidic linkage to serine or threonine residues. Since both phosphorylation and glycosylation compete for similar serine or threonine residues, the two processes may compete for sites, or they may alter the substrate specificity of nearby sites by steric or electrostatic effects. The protein contains multiple tetratricopeptide repeats that are required for optimal recognition of substrates. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2009]

OGT Products(2)

mRNA Protein Name
NM_181672.3 NP_858058.1 UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform 1
NM_181673.3 NP_858059.1 UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables phosphatidylinositol-3,4,5-trisphosphate binding IDA
IDA: Inferred from direct assay
18288188 GOA
enables protein O-acetylglucosaminyltransferase activity EXP
EXP: Inferred from Experiment
30770249 GOA
enables protein O-acetylglucosaminyltransferase activity IDA
IDA: Inferred from direct assay
21285374 GOA
enables protein O-acetylglucosaminyltransferase activity IMP
IMP: Inferred from mutant phenotype
23777819 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12150998 GOA
Biological Process GO Annotation Evidence Reference Source
involved in apoptotic process IDA
IDA: Inferred from direct assay
20824293 GOA
involved in cellular response to glucose stimulus IDA
IDA: Inferred from direct assay
37541260 GOA
involved in negative regulation of non-canonical inflammasome complex assembly IDA
IDA: Inferred from direct assay
37962578 GOA
involved in negative regulation of proteasomal ubiquitin-dependent protein catabolic process IMP
IMP: Inferred from mutant phenotype
26678539 GOA
involved in negative regulation of protein ubiquitination IMP
IMP: Inferred from mutant phenotype
26678539 GOA
involved in positive regulation of TORC1 signaling IDA
IDA: Inferred from direct assay
37541260 GOA
involved in positive regulation of proteolysis IDA
IDA: Inferred from direct assay
21285374 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
23222540 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
23352454 GOA
involved in positive regulation of translation IDA
IDA: Inferred from direct assay
34074792 GOA
involved in protein O-linked glycosylation IDA
IDA: Inferred from direct assay
21240259 GOA
involved in protein O-linked glycosylation IMP
IMP: Inferred from mutant phenotype
23353889 GOA
involved in protein processing IMP
IMP: Inferred from mutant phenotype
28584052 GOA
involved in regulation of Rac protein signal transduction IDA
IDA: Inferred from direct assay
18288188 GOA
involved in regulation of glycolytic process IDA
IDA: Inferred from direct assay
22923583 GOA
involved in regulation of insulin receptor signaling pathway IDA
IDA: Inferred from direct assay
18288188 GOA
involved in regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
26678539 GOA
involved in response to insulin IDA
IDA: Inferred from direct assay
18288188 GOA
Cellular Component GO Annotation Evidence Reference Source
part of NSL complex IDA
IDA: Inferred from direct assay
20018852 GOA
located in cytosol IDA
IDA: Inferred from direct assay
21285374 GOA
part of histone acetyltransferase complex IDA
IDA: Inferred from direct assay
20018852 GOA
located in nucleus IDA
IDA: Inferred from direct assay
21285374 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
18288188 GOA
part of protein N-acetylglucosaminyltransferase complex IDA
IDA: Inferred from direct assay
21240259 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
26678539 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

OGT Protein Structure

TPR_11

TPR_11: TPR repeat (88 - 154)

TPR_11

TPR_11: TPR repeat (162 - 222)

TPR_1

TPR_1: Tetratricopeptide repeat (226 - 258)

TPR_11

TPR_11: TPR repeat (268 - 324)

TPR_11

TPR_11: TPR repeat (327 - 392)

TPR_11

TPR_11: TPR repeat (395 - 443)

Glyco_transf_41

Glyco_transf_41: Glycosyl transferase family 41 (556 - 1024)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1046 a.a.
Protein Preferred Names Protein Names

UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit

O-GlcNAc transferase p110 subunit

OGT Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
OGT O15294 TET2 Homo sapiens E7EQS8
Y2H Prey Pooling
25416956
Intra
OGT O15294 TET2 Homo sapiens E7EQS8
Validated Y2H
25416956
Intra
OGT O15294 TRAK1 Homo sapiens Q9UPV9
TAP
27705803
Intra
OGT O15294 PHC3 Homo sapiens Q8NDX5
Y2H Prey Pooling
25416956
Intra
OGT O15294 PHC3 Homo sapiens Q8NDX5
Y2H Array
25416956
Intra
OGT O15294 TET2 Homo sapiens Q6N021-1
Pull Down
23222540
Intra
OGT O15294 TET3 Homo sapiens O43151
Pull Down
23353889
Intra
OGT O15294 TET3 Homo sapiens O43151
Pull Down
23222540
Intra
OGT O15294 TET2 Homo sapiens Q6N021
Anti Bait CoIP
23353889
Intra
OGT O15294 TET2 Homo sapiens Q6N021
Pull Down
23353889
Intra
OGT O15294 PPP1CC Homo sapiens P36873
Anti Bait CoIP
27505673
Intra
OGT O15294 URI1 Homo sapiens O94763
Anti Bait CoIP
27505673
Intra
OGT O15294 URI1 Homo sapiens O94763
Pull Down
27505673
Intra
OGT O15294 URI1 Homo sapiens O94763
Enzymatic Study
27505673
Intra
OGT O15294 URI1 Homo sapiens O94763
Anti Tag CoIP
27505673
Intra
OGT O15294 TAB1 Homo sapiens Q15750
Enzymatic Study
27505673
Cross
OGT O15294 Hoxa1 Mus musculus P09022
BiFC
23088713
Cross
OGT O15294 Hoxa1 Mus musculus P09022
Y2H
23088713
Intra
OGT O15294 HCFC1 Homo sapiens P51610
TAP
27705803
Intra
OGT O15294 HCFC1 Homo sapiens P51610
Protease Assay
21295698
Intra
OGT O15294 SNAP29 Homo sapiens O95721
Pull Down
25419848
Intra
OGT O15294 SNAP29 Homo sapiens O95721
Anti Tag CoIP
25419848
Intra
OGT O15294 NFATC1 Homo sapiens O95644
Anti Bait CoIP
17882263
Intra
OGT O15294 PSG1 Homo sapiens P11464
Y2H Prey Pooling
25416956
Intra
OGT O15294 PSG1 Homo sapiens P11464
Validated Y2H
25416956
Intra
OGT O15294 RELA Homo sapiens Q04206
Anti Bait CoIP
17882263
Intra
OGT O15294 NUP62CL Homo sapiens Q9H1M0
Y2H Prey Pooling
25416956
Intra
OGT O15294 NUP62CL Homo sapiens Q9H1M0
Y2H Pooling
16189514
Cross
OGT O15294 Tet3 Mus musculus Q8BG87
Pull Down
23353889
Cross
OGT O15294 Tet3 Mus musculus Q8BG87
Anti Tag CoIP
23353889
Cross
OGT O15294 Ppp1cc Rattus norvegicus P63088
Pull Down
27505673
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, X-Linked 106

XLID106

Mrx106

Mental Retardation, X-Linked 106

Mental Retardation, X-Linked, Type 106

Myoepithelioma

Benign Myoepithelioma

Myoepithelial Adenoma

Myoepithelial Neoplasm

Malignant Myoepithelioma

Bainbridge-Ropers Syndrome

BRPS

Severe Feeding Difficulties-Failure To Thrive-Microcephaly Due To Asxl3 Deficiency Syndrome

Asxl3-Related Disorder

Adams-Oliver Syndrome

Adams Oliver Syndrome

Aos

Congenital Scalp Defects With Distal Limb Reduction Anomalies

Aplasia Cutis Congenita With Terminal Transverse Limb Defects

Congenital Scalp Defects With Distal Limb Anomalies

Limb, Scalp And Skull Defects

Limb Scalp And Skull Defects

Absence Defect Of Limbs, Scalp, And Skull

Type 2 Diabetes Mellitus

Insulin Resistance

NIDDM

Type 2 Diabetes

Diabetes Mellitus, Non-Insulin-Dependent

T2D

Noninsulin-Dependent Diabetes Mellitus

Diabetes Mellitus, Type Ii

Maturity-Onset Diabetes

Insulin Resistance, Severe, Digenic

Diabetes Mellitus, Type 2

Diabetes Mellitus, Noninsulin-Dependent

Diabetes Mellitus, Noninsulin-Dependent, Association With

Diabetes Mellitus, Noninsulin-Dependent, Late Onset

Hypertension, Insulin Resistance-Related, Susceptibility To

Insulin Resistance, Susceptibility To

Non-Insulin-Dependent Diabetes Mellitus

Type Ii Diabetes Mellitus

Adult-Onset Diabetes Mellitus

Maturity-Onset Diabetes Mellitus

Diabetes Mellitus Type 2

Type Ii Diabetes

Type 2 Diabetes Mellitus, Susceptibility To

Diabetes, Type 2

Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

Diabetes Mellitus, Type 2, Susceptibility To

Diabetes Mellitus, Noninsulin-Dependent, 2

Diabetes Mellitus, Type Ii, Susceptibility To

Hypertension, Insulin Resistance-Related

Adult-Onset Diabetes

Aodm

Diabetes Mellitus, Adult-Onset

Diabetes Mellitus Type Ii

Diabetes Mellitus Type 2, Susceptibility To

Diabetes, Type Ii, Susceptibility To

Diabetes Type 2

Diabetes Mellitus

Adult Onset Diabetes

Maturity Onset Diabetes

Nonketotic Diabetes

Non-Insulin Dependent Diabetes Mellitus

T2dm - [Type 2 Diabetes Mellitus]

Niddm - [Non Insulin Dependent Diabetes Mellitus]

Dm2

Dm Type Ii

Diabetic Type 2

Insulin Requiring Type 2 Diabetes

Noninsulin Dependent Diabetes

Non-Insulin-Dependent Diabetes Mellitus Without Complications

Diabetes Due To Insulin Secretory Defect

Diabetes Mellitus Due To Insulin Secretory Defect

Non-Insulin-Dependent Diabetes Of The Young

Senile Diabetes

Nonketotic Hyperglycaemia

Stable Diabetes

Alzheimer Disease, Familial, 1

Alzheimer Disease

Alzheimer'S Disease

Presenile And Senile Dementia

AD1

Alzheimer Disease, Susceptibility To

Alzheimer Disease, Late-Onset, Susceptibility To

Alzheimer Disease 1, Familial

AD

Familial Alzheimer Disease

Alzheimer Disease, Late-Onset

Alzheimers Dementia

Alzheimer Dementia

Alzheimer Sclerosis

Alzheimer Syndrome

Alzheimer-Type Dementia

Dat

Primary Senile Degenerative Dementia

Sdat

Alzheimer Disease 1

Autosomal Dominant Alzheimer Disease

Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

Late Onset Alzheimer Disease

Alzheimers Disease

Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

Late-Onset Alzheimers Disease

Alzheimer'S Disease Pathway Kegg

Dementia Due To Alzheimer'S Disease

Alzheimer Disease Type 1

Alzheimers

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus OGT MGD MGI:1339639
Rattus norvegicus OGT RGD RGD:62060
Others OGT NCBI