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

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

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8473

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
Molecular Function GO Annotation Evidence References 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 References 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 References 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
  • 1000
  • 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 References
Intra
OGT O15294 TET2 Homo sapiens E7EQS8 25416956
Intra
OGT O15294 TET2 Homo sapiens E7EQS8 25416956
Intra
OGT O15294 TRAK1 Homo sapiens Q9UPV9
TAP
27705803
Intra
OGT O15294 PHC3 Homo sapiens Q8NDX5 25416956
Intra
OGT O15294 PHC3 Homo sapiens Q8NDX5 25416956
Intra
OGT O15294 TET2 Homo sapiens Q6N021-1 23222540
Intra
OGT O15294 TET3 Homo sapiens O43151 23353889
Intra
OGT O15294 TET3 Homo sapiens O43151 23222540
Intra
OGT O15294 TET2 Homo sapiens Q6N021 23353889
Intra
OGT O15294 TET2 Homo sapiens Q6N021 23353889
Intra
OGT O15294 PPP1CC Homo sapiens P36873 27505673
Intra
OGT O15294 URI1 Homo sapiens O94763 27505673
Intra
OGT O15294 URI1 Homo sapiens O94763 27505673
Intra
OGT O15294 URI1 Homo sapiens O94763 27505673
Intra
OGT O15294 URI1 Homo sapiens O94763 27505673
Intra
OGT O15294 TAB1 Homo sapiens Q15750 27505673
Cross
OGT O15294 Hoxa1 Mus musculus P09022 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 21295698
Intra
OGT O15294 SNAP29 Homo sapiens O95721 25419848
Intra
OGT O15294 SNAP29 Homo sapiens O95721 25419848
Intra
OGT O15294 NFATC1 Homo sapiens O95644 17882263
Intra
OGT O15294 PSG1 Homo sapiens P11464 25416956
Intra
OGT O15294 PSG1 Homo sapiens P11464 25416956
Intra
OGT O15294 RELA Homo sapiens Q04206 17882263
Intra
OGT O15294 NUP62CL Homo sapiens Q9H1M0 25416956
Intra
OGT O15294 NUP62CL Homo sapiens Q9H1M0 16189514
Cross
OGT O15294 Tet3 Mus musculus Q8BG87 23353889
Cross
OGT O15294 Tet3 Mus musculus Q8BG87 23353889
Cross
OGT O15294 Ppp1cc Rattus norvegicus P63088 27505673
Cross: Cross-species interaction Intra: Intraspecies interaction

OGT Antibodies

Cat. No. Product Name Application Reactivity
HY-P80254 OGT Antibody (YA257) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat

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