Pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) - Rat Genome Database

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Gene: Pomgnt1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)) Rattus norvegicus
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Symbol: Pomgnt1
Name: protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
RGD ID: 1359396
Description: Predicted to enable beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity and manganese ion binding activity. Predicted to be involved in O-glycan processing. Predicted to act upstream of or within several processes, including nervous system development; protein O-linked mannosylation; and reactive gliosis. Predicted to be located in membrane. Predicted to be active in Golgi membrane. Human ortholog(s) of this gene implicated in lissencephaly; muscular dystrophy (multiple); and retinitis pigmentosa. Orthologous to human POMGNT1 (protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)); PARTICIPATES IN O-linked glycan biosynthetic pathway; INTERACTS WITH 2,4-dinitrotoluene; 3,4-methylenedioxymethamphetamine; 4-amino-2,6-dinitrotoluene.
Type: protein-coding
RefSeq Status: PROVISIONAL
Previously known as: MGC94463; O-linked mannose beta1,2-N-acetylglucosaminyltransferase; protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85134,870,971 - 134,880,864 (+)NCBIGRCr8
mRatBN7.25129,634,274 - 129,644,150 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5129,634,294 - 129,644,149 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5132,250,551 - 132,260,368 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05134,005,138 - 134,014,956 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05134,027,575 - 134,037,392 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05135,007,343 - 135,017,220 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5135,007,343 - 135,017,218 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05138,791,235 - 138,801,112 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45136,429,379 - 136,439,254 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.15136,434,604 - 136,444,480 (+)NCBI
Celera5128,162,654 - 128,172,461 (+)NCBICelera
Cytogenetic Map5q35NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model



  
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Original Reference(s)
Pomgnt1RatGliosis  ISORGD:155316611532765 RGD 
Pomgnt1Ratlissencephaly  ISORGD:160199411065022DNA:frameshift mutations, missense mutations, deletion:exon, intron:multipleRGD 
Pomgnt1Ratmuscular dystrophy  ISORGD:16019941599152DNA:missense mutations, nonsense mutation, snp:exons, intron:multiple (human)RGD 
Pomgnt1RatWalker-Warburg syndrome  ISORGD:160199411532772DNA:missense mutations, nonsense mutation: :multipleRGD 
Pomgnt1RatWalker-Warburg syndrome  ISORGD:160199411065512DNA:deletions, splice-site mutation:exon, intron:multipleRGD 
Pomgnt1RatWalker-Warburg syndrome  ISORGD:16019941554293DNA:missense mutations, splice-site mutations, deletions: :multipleRGD 
Pomgnt1RatWalker-Warburg syndrome  ISORGD:160199411071487DNA:missense mutations:exon:p.R265H (935G>A), p.R311Q (1037G>A), p.C442R (1465C>T) (human)RGD 
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Original Reference(s)
Pomgnt1Ratautism spectrum disorder  ISORGD:16019948554872ClinVar Annotator: match by term: Autism spectrum disorderClinVarPMID:25741868
Pomgnt1Ratautosomal recessive limb-girdle muscular dystrophy  ISORGD:16019948554872ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy | ClinVar Annotator: match by more ...ClinVarPMID:11709191|PMID:12588800|PMID:15236414|PMID:15466003|PMID:15938569|PMID:16199547|PMID:16427280|PMID:17030669|PMID:17559086|PMID:17869517|PMID:17878207|PMID:17881266|PMID:17906881|PMID:18330676|PMID:19299310|PMID:19679478|PMID:20215985|PMID:20816175|PMID:21361872|PMID:21447391|PMID:22323514|PMID:22522420|PMID:23326386|PMID:23689641|PMID:23894383|PMID:24731844|PMID:25390965|PMID:25525159|PMID:25741868|PMID:26013959|PMID:26467025|PMID:26908613|PMID:26990548|PMID:27391550|PMID:27493216|PMID:27604308|PMID:28424332|PMID:28492532|PMID:28765568|PMID:29302074|PMID:30961548|PMID:31066047|PMID:31589614|PMID:31964843|PMID:31980526|PMID:32404165|PMID:33144682|PMID:33200426
Pomgnt1Ratautosomal recessive limb-girdle muscular dystrophy type 2O  ISORGD:16019948554872ClinVar Annotator: match by term: Autosomal recessive limb-girdle muscular dystrophy type 2O | ClinVar Annotator: more ...ClinVarPMID:11709191|PMID:12588800|PMID:12788071|PMID:12849864|PMID:15236414|PMID:15466003|PMID:15938569|PMID:16199547|PMID:16427280|PMID:17030669|PMID:17154333|PMID:17559086|PMID:17576681|PMID:17869517|PMID:17878207|PMID:17881266|PMID:17906881|PMID:18195152|PMID:18330676|PMID:18691338|PMID:19067344|PMID:19299310|PMID:19679478|PMID:20215985|PMID:20816175|PMID:20981092|PMID:21228398|PMID:21361872|PMID:21447391|PMID:21727005|PMID:22323514|PMID:22419172|PMID:22522420|PMID:22554691|PMID:22819665|PMID:22995991|PMID:23326386|PMID:23453855|PMID:23689641|PMID:23894383|PMID:24033266|PMID:24123366|PMID:24282183|PMID:24731844|PMID:24733390|PMID:25326635|PMID:25333069|PMID:25390965|PMID:25525159|PMID:25640679|PMID:25741868|PMID:25987458|PMID:26013959|PMID:26467025|PMID:26908613|PMID:26938784|PMID:26990548|PMID:27391550|PMID:27493216|PMID:27604308|PMID:27884173|PMID:28424332|PMID:28492532|PMID:28688748|PMID:28765568|PMID:28832562|PMID:29096039|PMID:29302074|PMID:29555514|PMID:30937090|PMID:30961548|PMID:31066047|PMID:31069529|PMID:3123072|PMID:31230720|PMID:31589614|PMID:31872526|PMID:31964843|PMID:31980526|PMID:32115343|PMID:32404165|PMID:33077954|PMID:33144682|PMID:33175337|PMID:33200426|PMID:33413009|PMID:34324503|PMID:34426522|PMID:35846108|PMID:36819107|PMID:36964972|PMID:9536098
Pomgnt1RatCharcot-Marie-Tooth disease dominant intermediate C  ISORGD:16019948554872ClinVar Annotator: match by term: Charcot-Marie-Tooth disease dominant intermediate CClinVarPMID:28492532
Pomgnt1Ratcongenital muscular dystrophy  ISORGD:16019948554872ClinVar Annotator: match by term: Congenital Muscular Dystrophy, alpha-dystroglycan related | ClinVar Annotator: match by more ...ClinVarPMID:17878207|PMID:18195152|PMID:18691338|PMID:19067344|PMID:20981092|PMID:21228398|PMID:21361872|PMID:21727005|PMID:22995991|PMID:24033266|PMID:24123366|PMID:25326635|PMID:25333069|PMID:25741868|PMID:26467025|PMID:27884173|PMID:28492532
Pomgnt1Ratcongenital muscular dystrophy-dystroglycanopathy type A  ISORGD:16019948554872ClinVar Annotator: match by term: Congenital muscular alpha-dystroglycanopathy with brain and eye anomaliesClinVarPMID:11709191|PMID:12588800|PMID:15466003|PMID:16199547|PMID:16427280|PMID:17559086|PMID:17878207|PMID:17881266|PMID:17906881|PMID:19299310|PMID:20816175|PMID:21447391|PMID:22323514|PMID:23326386|PMID:25525159|PMID:25741868|PMID:26013959|PMID:26908613|PMID:26990548|PMID:27391550|PMID:27604308|PMID:28492532|PMID:30961548|PMID:31589614|PMID:31980526|PMID:33144682
Pomgnt1Ratcongenital muscular dystrophy-dystroglycanopathy type A3  ISORGD:16019948554872ClinVar Annotator: match by term: Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A3 more ...ClinVarPMID:11709191|PMID:12588800|PMID:12788071|PMID:12849864|PMID:15236414|PMID:15466003|PMID:15938569|PMID:16199547|PMID:16427280|PMID:17030669|PMID:17154333|PMID:17559086|PMID:17576681|PMID:17869517|PMID:17878207|PMID:17881266|PMID:17906881|PMID:18195152|PMID:18330676|PMID:18691338|PMID:19067344|PMID:19299310|PMID:19679478|PMID:20215985|PMID:20816175|PMID:20981092|PMID:21228398|PMID:21361872|PMID:21447391|PMID:21727005|PMID:21983716|PMID:22323514|PMID:22522420|PMID:22554691|PMID:22995991|PMID:23326386|PMID:23453855|PMID:23689641|PMID:23894383|PMID:24033266|PMID:24123366|PMID:24282183|PMID:24731844|PMID:24733390|PMID:25333069|PMID:25390965|PMID:25525159|PMID:25741868|PMID:26013959|PMID:26467025|PMID:26908613|PMID:26938784|PMID:26990548|PMID:27391550|PMID:27493216|PMID:27604308|PMID:27884173|PMID:28424332|PMID:28492532|PMID:28688748|PMID:28832562|PMID:29302074|PMID:29555514|PMID:30961548|PMID:31066047|PMID:31589614|PMID:31964843|PMID:31980526|PMID:32404165|PMID:33144682|PMID:33200426|PMID:34324503|PMID:36819107|PMID:36964972|PMID:9536098
Pomgnt1Ratdevelopmental and epileptic encephalopathy  ISORGD:16019948554872ClinVar Annotator: match by term: Developmental and epileptic encephalopathyClinVarPMID:28492532
Pomgnt1Ratearly infantile epileptic encephalopathy  ISORGD:16019948554872ClinVar Annotator: match by term: Early infantile epileptic encephalopathyClinVarPMID:28492532
Pomgnt1Ratfundus dystrophy  ISORGD:16019948554872ClinVar Annotator: match by term: Retinal dystrophyClinVarPMID:11709191|PMID:12588800|PMID:12849864|PMID:15236414|PMID:15466003|PMID:16199547|PMID:16427280|PMID:17559086|PMID:17878207|PMID:17881266|PMID:17906881|PMID:19299310|PMID:20816175|PMID:21361872|PMID:21447391|PMID:22323514|PMID:22819665|PMID:23326386|PMID:23453855|PMID:23689641|PMID:24033266|PMID:25390965|PMID:25525159|PMID:25741868|PMID:26013959|PMID:26467025|PMID:26908613|PMID:26990548|PMID:27391550|PMID:27493216|PMID:27604308|PMID:28492532|PMID:29096039|PMID:29302074|PMID:30937090|PMID:30961548|PMID:31066047|PMID:3123072|PMID:31230720|PMID:31589614|PMID:31964843|PMID:31980526|PMID:32404165|PMID:33144682|PMID:33200426|PMID:34426522
Pomgnt1Ratgenetic disease  ISORGD:16019948554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:15466003|PMID:17576681|PMID:19299310|PMID:20816175|PMID:21447391|PMID:22323514|PMID:22554691|PMID:22819665|PMID:25741868|PMID:26467025|PMID:26908613|PMID:27391550|PMID:27493216|PMID:28424332|PMID:28492532|PMID:28688748|PMID:29096039|PMID:29555514|PMID:33413009|PMID:9536098
Pomgnt1Rathydrocephalus  ISORGD:16019948554872ClinVar Annotator: match by term: HydrocephalusClinVarPMID:25741868
Pomgnt1Ratintellectual disability  ISORGD:16019948554872ClinVar Annotator: match by term: Intellectual disabilityClinVarPMID:17878207|PMID:25741868|PMID:28492532|PMID:36964972
Pomgnt1Ratlimb-girdle muscular dystrophy  ISORGD:16019948554872ClinVar Annotator: match by term: Limb-girdle muscular dystrophyClinVar 
Pomgnt1RatMuscle Hypotonia  ISORGD:16019948554872ClinVar Annotator: match by term: HypotoniaClinVar 
Pomgnt1Ratmuscular dystrophy-dystroglycanopathy  ISORGD:16019948554872ClinVar Annotator: match by term: Congenital muscular dystrophy due to dystroglycanopathy | ClinVar Annotator: match more ...ClinVarPMID:11709191|PMID:12588800|PMID:12788071|PMID:12849864|PMID:15236414|PMID:15466003|PMID:15938569|PMID:16199547|PMID:16427280|PMID:17030669|PMID:17154333|PMID:17559086|PMID:17576681|PMID:17869517|PMID:17878207|PMID:17881266|PMID:17906881|PMID:18195152|PMID:18330676|PMID:19067344|PMID:19299310|PMID:19679478|PMID:20215985|PMID:20816175|PMID:21361872|PMID:21447391|PMID:21727005|PMID:22323514|PMID:22522420|PMID:22554691|PMID:22819665|PMID:23326386|PMID:23453855|PMID:23689641|PMID:23894383|PMID:24282183|PMID:24731844|PMID:25390965|PMID:25525159|PMID:25741868|PMID:26013959|PMID:26467025|PMID:26908613|PMID:26938784|PMID:26990548|PMID:27391550|PMID:27493216|PMID:27604308|PMID:28424332|PMID:28492532|PMID:28688748|PMID:28832562|PMID:29096039|PMID:29302074|PMID:29555514|PMID:30937090|PMID:30961548|PMID:31066047|PMID:31069529|PMID:31230720|PMID:31589614|PMID:31964843|PMID:31980526|PMID:32404165|PMID:33144682|PMID:33175337|PMID:33200426|PMID:34324503|PMID:34426522|PMID:36964972|PMID:9536098
Pomgnt1Ratmuscular dystrophy-dystroglycanopathy type B3  ISORGD:16019948554872ClinVar Annotator: match by term: MUSCULAR DYSTROPHY, CONGENITAL, POMGNT1-RELATEDClinVarPMID:11709191|PMID:12588800|PMID:15236414|PMID:15466003|PMID:16199547|PMID:16427280|PMID:17030669|PMID:17559086|PMID:17576681|PMID:17878207|PMID:17881266|PMID:17906881|PMID:18195152|PMID:18330676|PMID:18691338|PMID:19067344|PMID:19299310|PMID:19679478|PMID:20816175|PMID:20981092|PMID:21228398|PMID:21361872|PMID:21447391|PMID:21727005|PMID:22323514|PMID:22554691|PMID:22995991|PMID:23326386|PMID:23689641|PMID:24033266|PMID:24123366|PMID:24282183|PMID:24731844|PMID:25333069|PMID:25390965|PMID:25525159|PMID:25741868|PMID:26013959|PMID:26467025|PMID:26908613|PMID:26938784|PMID:26990548|PMID:27391550|PMID:27493216|PMID:27604308|PMID:27884173|PMID:28424332|PMID:28492532|PMID:28688748|PMID:28832562|PMID:29555514|PMID:30937090|PMID:30961548|PMID:31069529|PMID:3123072|PMID:31230720|PMID:31589614|PMID:31964843|PMID:31980526|PMID:33144682|PMID:34324503|PMID:34426522|PMID:9536098
Pomgnt1Ratmuscular dystrophy-dystroglycanopathy type B6  ISORGD:16019948554872ClinVar Annotator: match by term: Muscular dystrophy-dystroglycanopathy type B6ClinVarPMID:17878207|PMID:25741868|PMID:28492532|PMID:36964972
Pomgnt1RatNervous System Malformations  ISORGD:16019948554872ClinVar Annotator: match by term: Abnormality of the nervous systemClinVarPMID:25741868
Pomgnt1Ratoptic atrophy  ISORGD:16019948554872ClinVar Annotator: match by term: Optic atrophyClinVarPMID:25741868|PMID:28492532
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Pomgnt1RatWalker-Warburg syndrome  ISORGD:160199411554173CTD Direct Evidence: marker/mechanismCTD 
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Pomgnt1Ratmuscular dystrophy-dystroglycanopathy type B1  ISSRGD:160199413592920OMIM:613151 | OMIM:613152 | OMIM:613155 | OMIM:613156 | OMIM:615351 | OMIM:616094MouseDO 
Pomgnt1RatWalker-Warburg syndrome  ISSRGD:155316613592920 MouseDO 
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Pomgnt1Ratautosomal recessive limb-girdle muscular dystrophy type 2O  ISORGD:16019947240710 OMIM 
Pomgnt1Ratcongenital muscular dystrophy-dystroglycanopathy type A3  ISORGD:16019947240710 OMIM 
Pomgnt1Ratmuscular dystrophy-dystroglycanopathy type B3  ISORGD:16019947240710 OMIM 
Pomgnt1Ratretinitis pigmentosa 76  ISORGD:16019947240710 OMIM 

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Pomgnt1Rat1,2-dimethylhydrazine increases expressionISORGD:155316664804641,2-Dimethylhydrazine results in increased expression of POMGNT1 mRNACTDPMID:22206623
Pomgnt1Rat17alpha-ethynylestradiol affects expressionISORGD:15531666480464Ethinyl Estradiol affects the expression of POMGNT1 mRNACTDPMID:17555576
Pomgnt1Rat17beta-estradiol increases expressionISORGD:16019946480464Estradiol results in increased expression of POMGNT1 mRNACTDPMID:19167446
Pomgnt1Rat2,3,7,8-tetrachlorodibenzodioxine increases expressionISORGD:15531666480464Tetrachlorodibenzodioxin results in increased expression of POMGNT1 mRNACTDPMID:15328365
Pomgnt1Rat2,3,7,8-tetrachlorodibenzodioxine multiple interactionsISORGD:15531666480464[TIPARP gene mutant form results in increased susceptibility to Tetrachlorodibenzodioxin] which results in decreased expression more ...CTDPMID:25975270
Pomgnt1Rat2,3,7,8-tetrachlorodibenzodioxine affects expressionISORGD:15531666480464Tetrachlorodibenzodioxin affects the expression of POMGNT1 mRNACTDPMID:18343893|PMID:21570461
Pomgnt1Rat2,3,7,8-Tetrachlorodibenzofuran affects expressionISORGD:155316664804642,3,7,8-tetrachlorodibenzofuran affects the expression of POMGNT1 mRNACTDPMID:18343893
Pomgnt1Rat2,4-dinitrotoluene affects expressionEXP 64804642,4-dinitrotoluene affects the expression of POMGNT1 mRNACTDPMID:21346803
Pomgnt1Rat3,4-methylenedioxymethamphetamine increases expressionISORGD:15531666480464N-Methyl-3,4-methylenedioxyamphetamine results in increased expression of POMGNT1 mRNACTDPMID:20188158
Pomgnt1Rat3,4-methylenedioxymethamphetamine decreases expressionEXP 6480464N-Methyl-3,4-methylenedioxyamphetamine results in decreased expression of POMGNT1 mRNACTDPMID:30071829
Pomgnt1Rat4,4'-sulfonyldiphenol decreases expressionISORGD:15531666480464bisphenol S results in decreased expression of POMGNT1 mRNACTDPMID:39298647
Pomgnt1Rat4-amino-2,6-dinitrotoluene affects expressionEXP 64804644-amino-2,6-dinitrotoluene affects the expression of POMGNT1 mRNACTDPMID:21346803
Pomgnt1Ratacrylamide decreases expressionISORGD:16019946480464Acrylamide results in decreased expression of POMGNT1 mRNACTDPMID:32763439
Pomgnt1Rataflatoxin B1 increases methylationISORGD:16019946480464Aflatoxin B1 results in increased methylation of POMGNT1 geneCTDPMID:27153756
Pomgnt1Ratatrazine decreases expressionISORGD:16019946480464Atrazine results in decreased expression of POMGNT1 mRNACTDPMID:22378314
Pomgnt1Ratbenzo[a]pyrene affects methylationISORGD:16019946480464Benzo(a)pyrene affects the methylation of POMGNT1 3' UTRCTDPMID:27901495
Pomgnt1Ratbisphenol A decreases expressionISORGD:16019946480464bisphenol A results in decreased expression of POMGNT1 mRNACTDPMID:25047013
Pomgnt1Ratbisphenol A increases expressionISORGD:15531666480464bisphenol A results in increased expression of POMGNT1 mRNACTDPMID:32156529|PMID:33221593
Pomgnt1Ratbisphenol A decreases expressionEXP 6480464bisphenol A results in decreased expression of POMGNT1 mRNACTDPMID:30816183|PMID:32528016|PMID:34947998
Pomgnt1Ratbisphenol A decreases methylationISORGD:15531666480464bisphenol A results in decreased methylation of POMGNT1 promoterCTDPMID:27312807

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Biological Process
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Pomgnt1Ratbasement membrane organization acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratbasement membrane organization acts_upstream_of_or_withinISORGD:15531661624291MGI:3623521 PMID:21970971RGDPMID:21970971
Pomgnt1Ratbiological_process  ND 159840709/2016: no relevant rat dataRGD 
Pomgnt1Ratbrain development acts_upstream_of_or_withinISORGD:15531661624291MGI:5052171 PMID:26306834RGDPMID:26306834
Pomgnt1Ratbrain development acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratdentate gyrus development acts_upstream_of_or_withinISORGD:15531661624291MGI:3623521 PMID:21970971RGDPMID:21970971
Pomgnt1Ratdentate gyrus development acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratgene expression acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratgene expression acts_upstream_of_or_withinISORGD:15531661624291MGI:3623521|MGI:3832592 PMID:21129441, PMID:22270369, PMID:32453729RGDPMID:21129441|PMID:22270369|PMID:32453729
Pomgnt1Ratlocalization of cell acts_upstream_of_or_withinISORGD:15531661624291MGI:5052171 PMID:26306834RGDPMID:26306834
Pomgnt1Ratlocalization of cell acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratmyelination acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratmyelination acts_upstream_of_or_withinISORGD:15531661624291MGI:3832592 PMID:32453729RGDPMID:32453729
Pomgnt1RatO-glycan processing involved_inIEAUniProtKB:Q8WZA1|ensembl:ENSP000003610521600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1RatO-glycan processing involved_inIBAPANTHER:PTN000825782|UniProtKB:Q8WZA11600115GO_REF:0000033GO_CentralGO_REF:0000033
Pomgnt1RatO-glycan processing involved_inISORGD:16019941624291 PMID:27493216RGDPMID:27493216
Pomgnt1RatO-glycan processing involved_inISSUniProtKB:Q8WZA11600115GO_REF:0000024UniProtGO_REF:0000024
Pomgnt1Ratprotein glycosylation involved_inIEAUniPathway:UPA003781600115GO_REF:0000041UniProtGO_REF:0000041
Pomgnt1Ratprotein glycosylation acts_upstream_of_or_withinIEAUniProtKB:Q91X88|ensembl:ENSMUSP000001127511600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratprotein glycosylation acts_upstream_of_or_withinISORGD:15531661624291MGI:3623521|MGI:3832592 PMID:22728091, PMID:32453729RGDPMID:22728091|PMID:32453729
1 to 20 of 33 rows

Cellular Component
1 to 11 of 11 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Pomgnt1RatGolgi apparatus located_inIEAUniProtKB-KW:KW-03331600115GO_REF:0000043UniProtGO_REF:0000043
Pomgnt1RatGolgi membrane is_active_inIBAPANTHER:PTN000825782|UniProtKB:Q8WZA11600115GO_REF:0000033GO_CentralGO_REF:0000033
Pomgnt1RatGolgi membrane located_inIEAUniProtKB:Q8WZA1|ensembl:ENSP000003610521600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1RatGolgi membrane located_inIEAUniRule:UR0015907731600115GO_REF:0000104UniProtGO_REF:0000104
Pomgnt1RatGolgi membrane located_inISORGD:16019941624291 PMID:17034757RGDPMID:17034757
Pomgnt1RatGolgi membrane located_inISSUniProtKB:Q8WZA11600115GO_REF:0000024UniProtGO_REF:0000024
Pomgnt1RatGolgi membrane located_inIEAUniProtKB-SubCell:SL-01341600115GO_REF:0000044UniProtGO_REF:0000044
Pomgnt1Ratmembrane located_inIEAUniProtKB-KW:KW-04721600115GO_REF:0000043UniProtGO_REF:0000043
Pomgnt1Ratmembrane located_inIEAUniProtKB:Q8WZA1|ensembl:ENSP000003610521600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratmembrane located_inISORGD:16019941624291 PMID:27493216RGDPMID:27493216
Pomgnt1Ratmembrane located_inISSUniProtKB:Q8WZA11600115GO_REF:0000024UniProtGO_REF:0000024
1 to 11 of 11 rows

Molecular Function
1 to 19 of 19 rows

  
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Pomgnt1Ratacetylglucosaminyltransferase activity enablesIEAUniRule:UR0015907731600115GO_REF:0000104UniProtGO_REF:0000104
Pomgnt1Ratacetylglucosaminyltransferase activity enablesIEAUniProtKB:Q8WZA1|ensembl:ENSP000003610521600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratacetylglucosaminyltransferase activity enablesIEAInterPro:IPR0041391600115GO_REF:0000002InterProGO_REF:0000002
Pomgnt1Ratacetylglucosaminyltransferase activity enablesISORGD:16019941624291 PMID:26908613, PMID:27391550, PMID:27493216RGDPMID:26908613|PMID:27391550|PMID:27493216
Pomgnt1Ratacetylglucosaminyltransferase activity enablesISSUniProtKB:Q8WZA11600115GO_REF:0000024UniProtGO_REF:0000024
Pomgnt1Ratalpha-1,3-mannosylglycoprotein 2-beta-N-acetylglucosaminyltransferase activity enablesIEAUniRule:UR0015907731600115GO_REF:0000104UniProtGO_REF:0000104
Pomgnt1Ratbeta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity enablesISORGD:16019941624291 PMID:11742540RGDPMID:11742540
Pomgnt1Ratbeta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity enablesIBAPANTHER:PTN000825782|UniProtKB:Q8WZA11600115GO_REF:0000033GO_CentralGO_REF:0000033
Pomgnt1Ratbeta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase activity enablesIEAUniProtKB:Q8WZA1|ensembl:ENSP000003610521600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratcarbohydrate binding enablesIEAUniRule:UR0019229811600115GO_REF:0000104UniProtGO_REF:0000104
Pomgnt1Ratcarbohydrate binding enablesIEAUniProtKB-KW:KW-04301600115GO_REF:0000043UniProtGO_REF:0000043
Pomgnt1Ratglycosyltransferase activity enablesIEAUniProtKB-KW:KW-03281600115GO_REF:0000043UniProtGO_REF:0000043
Pomgnt1Ratmanganese ion binding enablesIEAUniRule:UR0015907731600115GO_REF:0000104UniProtGO_REF:0000104
Pomgnt1Ratmanganese ion binding enablesISORGD:16019941624291 PMID:27493216RGDPMID:27493216
Pomgnt1Ratmanganese ion binding enablesIEAUniProtKB:Q8WZA1|ensembl:ENSP000003610521600115GO_REF:0000107EnsemblGO_REF:0000107
Pomgnt1Ratmanganese ion binding enablesISSUniProtKB:Q8WZA11600115GO_REF:0000024UniProtGO_REF:0000024
Pomgnt1Ratmetal ion binding enablesIEAUniProtKB-KW:KW-04791600115GO_REF:0000043UniProtGO_REF:0000043
Pomgnt1Ratprotein binding enablesISORGD:16019941624291UniProtKB:O75072|UniProtKB:P04233-2|UniProtKB:Q5JRM2|UniProtKB:Q8N5K1|UniProtKB:Q8TBB1|UniProtKB:Q96Q45-2|UniProtKB:Q9H5K3|UniProtKB:Q9Y282|UniProtKB:Q9Y2B1 PMID:17034757, PMID:25416956, PMID:28514442, PMID:29892012, PMID:32296183, PMID:32707033, PMID:33961781RGDPMID:17034757|PMID:25416956|PMID:28514442|PMID:29892012|PMID:32296183|PMID:32707033|PMID:33961781
Pomgnt1Rattransferase activity enablesIEAUniProtKB-KW:KW-08081600115GO_REF:0000043UniProtGO_REF:0000043
1 to 19 of 19 rows

Imported Annotations - KEGG (archival)

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
Pomgnt1RatO-linked glycan biosynthetic pathway  IEA 6907045 KEGGrno:00514

1 to 16 of 16 rows
#
Reference Title
Reference Citation
1. POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum. Biancheri R, etal., Arch Neurol. 2006 Oct;63(10):1491-5.
2. Molecular heterogeneity in fetal forms of type II lissencephaly. Bouchet C, etal., Hum Mutat. 2007 Oct;28(10):1020-7.
3. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
4. Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patients. Jiao H, etal., Mol Genet Genomics. 2013 Aug;288(7-8):297-308. doi: 10.1007/s00438-013-0749-5. Epub 2013 May 21.
5. Breaches of the pial basement membrane are associated with defective dentate gyrus development in mouse models of congenital muscular dystrophies. Li J, etal., Neurosci Lett. 2011 Nov 7;505(1):19-24. doi: 10.1016/j.neulet.2011.09.040. Epub 2011 Sep 29.
6. Rat ISS GO annotations from MGI mouse gene data--August 2006 MGD data from the GO Consortium
7. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
8. KEGG Annotation Import Pipeline Pipeline to import KEGG annotations from KEGG into RGD
9. GOA pipeline RGD automated data pipeline
10. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
11. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
12. Comprehensive gene review and curation RGD comprehensive gene curation
13. Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease. Saredi S, etal., J Neurol Sci. 2012 Jul 15;318(1-2):45-50. doi: 10.1016/j.jns.2012.04.008. Epub 2012 May 2.
14. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, etal., Proc Natl Acad Sci U S A. 2002 Dec 24;99(26):16899-903. Epub 2002 Dec 11.
15. POMGnT1 gene alterations in a family with neurological abnormalities. Vervoort VS, etal., Ann Neurol. 2004 Jul;56(1):143-8.
16. Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1. Yoshida A, etal., Dev Cell 2001 Nov;1(5):717-24.
1 to 16 of 16 rows
PMID:11742540   PMID:15489334   PMID:16458488   PMID:17034757   PMID:26908613   PMID:27391550   PMID:27493216  



Pomgnt1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr85134,870,971 - 134,880,864 (+)NCBIGRCr8
mRatBN7.25129,634,274 - 129,644,150 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl5129,634,294 - 129,644,149 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx5132,250,551 - 132,260,368 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.05134,005,138 - 134,014,956 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.05134,027,575 - 134,037,392 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.05135,007,343 - 135,017,220 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl5135,007,343 - 135,017,218 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.05138,791,235 - 138,801,112 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.45136,429,379 - 136,439,254 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.15136,434,604 - 136,444,480 (+)NCBI
Celera5128,162,654 - 128,172,461 (+)NCBICelera
Cytogenetic Map5q35NCBI
POMGNT1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38146,188,683 - 46,220,305 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl146,188,683 - 46,220,305 (-)EnsemblGRCh38hg38GRCh38
GRCh37146,654,355 - 46,685,977 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36146,426,940 - 46,436,708 (-)NCBINCBI36Build 36hg18NCBI36
Celera144,941,643 - 44,973,721 (-)NCBICelera
Cytogenetic Map1p34.1NCBI
HuRef144,769,330 - 44,801,277 (-)NCBIHuRef
CHM1_1146,771,477 - 46,803,118 (-)NCBICHM1_1
T2T-CHM13v2.0146,065,903 - 46,097,522 (-)NCBIT2T-CHM13v2.0
Pomgnt1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm394116,007,700 - 116,017,041 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl4115,981,037 - 116,017,046 (+)EnsemblGRCm39 Ensembl
GRCm384116,150,498 - 116,159,844 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl4116,123,840 - 116,159,849 (+)EnsemblGRCm38mm10GRCm38
MGSCv374115,823,123 - 115,832,449 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv364115,648,457 - 115,657,776 (+)NCBIMGSCv36mm8
Celera4114,888,693 - 114,898,002 (+)NCBICelera
Cytogenetic Map4D1NCBI
cM Map453.1NCBI
Pomgnt1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495546412,077,406 - 12,086,700 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495546412,076,815 - 12,086,961 (+)NCBIChiLan1.0ChiLan1.0
POMGNT1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21180,584,412 - 180,616,625 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11179,726,026 - 179,758,221 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0145,494,834 - 45,525,804 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1146,849,528 - 46,859,137 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl146,849,528 - 46,859,137 (-)Ensemblpanpan1.1panPan2
POMGNT1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11514,176,932 - 14,187,181 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1514,178,357 - 14,187,161 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1514,299,079 - 14,309,089 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01514,329,378 - 14,339,540 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1514,329,801 - 14,339,540 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11514,130,602 - 14,140,611 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01514,199,089 - 14,209,095 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01514,268,643 - 14,278,728 (+)NCBIUU_Cfam_GSD_1.0
Pomgnt1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505861,404,486 - 61,417,843 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493647427,229,113 - 27,239,123 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493647427,229,262 - 27,239,034 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
POMGNT1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl6165,212,833 - 165,222,409 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.16165,212,828 - 165,222,412 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.26152,692,300 - 152,701,877 (+)NCBISscrofa10.2Sscrofa10.2susScr3
POMGNT1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12086,588,049 - 86,597,576 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2086,588,550 - 86,599,107 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603330,389,152 - 30,398,705 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Pomgnt1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249062,119,684 - 2,135,656 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249062,120,759 - 2,131,024 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

.

.
Variants in Pomgnt1
39 total Variants

Predicted Target Of
Summary Value
Count of predictions:83
Count of miRNA genes:66
Interacting mature miRNAs:82
Transcripts:ENSRNOT00000035312
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 51 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1549845Scl44Serum cholesterol level QTL 446blood cholesterol amount (VT:0000180)serum total cholesterol level (CMO:0000363)540128307148607290Rat
8552960Pigfal15Plasma insulin-like growth factor 1 level QTL 15blood insulin-like growth factor amount (VT:0010479)plasma insulin-like growth factor 1 level (CMO:0001299)5111416838156416838Rat
1300122Wbc1White blood cell count QTL 12.75leukocyte quantity (VT:0000217)total white blood cell count (CMO:0000365)5125392826139989768Rat
61452Ciaa5CIA Autoantibody QTL 53.5blood autoantibody amount (VT:0003725)calculated serum anti-rat type 2 collagen autoantibody titer (CMO:0001281)594858972143070159Rat
70156Niddm30Non-insulin dependent diabetes mellitus QTL 303.98blood glucose amount (VT:0000188)blood glucose level area under curve (AUC) (CMO:0000350)5129132447151006154Rat
7411582Foco3Food consumption QTL 37.50.001eating behavior trait (VT:0001431)feed conversion ratio (CMO:0001312)587468046132468046Rat
1302790Scl20Serum cholesterol level QTL 206.40.0001blood cholesterol amount (VT:0000180)plasma total cholesterol level (CMO:0000585)582394392166664054Rat
1598861Cm64Cardiac mass QTL 642.9heart mass (VT:0007028)heart weight to body weight ratio (CMO:0000074)5127798274166875058Rat
1578766Tcas11Tongue tumor susceptibility QTL 114.12tongue integrity trait (VT:0010553)number of squamous cell tumors of the tongue with diameter greater than 3 mm (CMO:0001950)546711509161317411Rat
1549838Bss4Bone structure and strength QTL 49.2femur strength trait (VT:0010010)femur midshaft polar moment of inertia (CMO:0001669)5106906205151906205Rat

1 to 10 of 51 rows
MARC_7377-7378:992008389:1  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.25129,639,150 - 129,639,535 (+)MAPPERmRatBN7.2
Rnor_6.05135,012,219 - 135,012,603NCBIRnor6.0
Rnor_5.05138,796,111 - 138,796,495UniSTSRnor5.0
RGSC_v3.45136,434,255 - 136,434,639UniSTSRGSC3.4
Celera5128,167,462 - 128,167,846UniSTS
Cytogenetic Map5q36UniSTS




alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
9 11 49 113 91 90 59 25 59 6 218 97 93 45 60 31



Ensembl Acc Id: ENSRNOT00000035312   ⟹   ENSRNOP00000035825
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,634,301 - 129,644,015 (+)Ensembl
Rnor_6.0 Ensembl5135,007,343 - 135,017,218 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000098939   ⟹   ENSRNOP00000091939
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,634,306 - 129,644,132 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000101655   ⟹   ENSRNOP00000093130
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,634,306 - 129,644,132 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000107786   ⟹   ENSRNOP00000088565
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,635,186 - 129,644,132 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000108219   ⟹   ENSRNOP00000084795
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,634,294 - 129,644,149 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000109490   ⟹   ENSRNOP00000095021
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,635,186 - 129,644,132 (+)Ensembl
Ensembl Acc Id: ENSRNOT00000115433   ⟹   ENSRNOP00000093579
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 Ensembl5129,634,306 - 129,644,132 (+)Ensembl
RefSeq Acc Id: NM_001007747   ⟹   NP_001007748
RefSeq Status: PROVISIONAL
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr85134,870,989 - 134,880,864 (+)NCBI
mRatBN7.25129,634,274 - 129,644,150 (+)NCBI
Rnor_6.05135,007,343 - 135,017,218 (+)NCBI
Rnor_5.05138,791,235 - 138,801,112 (+)NCBI
RGSC_v3.45136,429,379 - 136,439,254 (+)RGD
Celera5128,162,654 - 128,172,461 (+)RGD
Sequence:
RefSeq Acc Id: XM_006238683   ⟹   XP_006238745
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr85134,871,821 - 134,880,864 (+)NCBI
mRatBN7.25129,635,091 - 129,644,150 (+)NCBI
Rnor_6.05135,008,072 - 135,017,220 (+)NCBI
Rnor_5.05138,791,235 - 138,801,112 (+)NCBI
Sequence:
RefSeq Acc Id: XM_063287979   ⟹   XP_063144049
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr85134,870,971 - 134,880,864 (+)NCBI
1 to 11 of 11 rows
Protein RefSeqs NP_001007748 (Get FASTA)   NCBI Sequence Viewer  
  XP_006238745 (Get FASTA)   NCBI Sequence Viewer  
  XP_063144049 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH83641 (Get FASTA)   NCBI Sequence Viewer  
  EDL90286 (Get FASTA)   NCBI Sequence Viewer  
  EDL90287 (Get FASTA)   NCBI Sequence Viewer  
  EDL90288 (Get FASTA)   NCBI Sequence Viewer  
  EDL90289 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000035825
  ENSRNOP00000095021
GenBank Protein Q5XIN7 (Get FASTA)   NCBI Sequence Viewer  
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RefSeq Acc Id: NP_001007748   ⟸   NM_001007747
- UniProtKB: Q5XIN7 (UniProtKB/Swiss-Prot),   A0A8L2QK62 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_006238745   ⟸   XM_006238683
- Peptide Label: isoform X2
- UniProtKB: A0A8I6AMP8 (UniProtKB/TrEMBL),   A6JZ66 (UniProtKB/TrEMBL),   A0A8L2QK62 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSRNOP00000035825   ⟸   ENSRNOT00000035312
Ensembl Acc Id: ENSRNOP00000093130   ⟸   ENSRNOT00000101655
Ensembl Acc Id: ENSRNOP00000095021   ⟸   ENSRNOT00000109490
GG-type lectin   ILEI/PANDER

Name Modeler Protein Id AA Range Protein Structure
AF-Q5XIN7-F1-model_v2 AlphaFold Q5XIN7 1-660 view protein structure


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen

RGD ID:13693930
Promoter ID:EPDNEW_R4455
Type:initiation region
Name:Pomgnt1_1
Description:protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta1,2-)
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.05135,007,329 - 135,007,389EPDNEW


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Database
Acc Id
Source(s)
BioCyc Gene G2FUF-40263 BioCyc
BioCyc Pathway PWY-7922 [protein O-mannosylation II (mammals, core M1 and core M2)] BioCyc
BioCyc Pathway Image PWY-7922 BioCyc
Ensembl Genes ENSRNOG00000023455 Ensembl, ENTREZGENE
Ensembl Transcript ENSRNOT00000035312 ENTREZGENE
  ENSRNOT00000109490 ENTREZGENE
Gene3D-CATH Spore Coat Polysaccharide Biosynthesis Protein SpsA, Chain A UniProtKB/Swiss-Prot
IMAGE_CLONE IMAGE:7134894 IMAGE-MGC_LOAD
InterPro Glyco_trans_13 UniProtKB/Swiss-Prot
  ILEI/PANDER_dom UniProtKB/Swiss-Prot
  Nucleotide-diphossugar_trans UniProtKB/Swiss-Prot
  O-linked_mannose_GnT UniProtKB/Swiss-Prot
  POMGNT1_PANDER-like UniProtKB/Swiss-Prot
KEGG Report rno:362567 UniProtKB/Swiss-Prot
MGC_CLONE MGC:94463 IMAGE-MGC_LOAD
NCBI Gene 362567 ENTREZGENE
PANTHER PROTEIN O-LINKED-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE 1 UniProtKB/Swiss-Prot
  PROTEIN O-LINKED-MANNOSE BETA-1,2-N-ACETYLGLUCOSAMINYLTRANSFERASE 1 UniProtKB/Swiss-Prot
Pfam GNT-I UniProtKB/Swiss-Prot
  ILEI UniProtKB/Swiss-Prot
PhenoGen Pomgnt1 PhenoGen
PROSITE GG_LECTIN UniProtKB/Swiss-Prot
RatGTEx ENSRNOG00000023455 RatGTEx
Superfamily-SCOP SSF53448 UniProtKB/Swiss-Prot
UniProt A0A8I6A0W0_RAT UniProtKB/TrEMBL
  A0A8I6AB13_RAT UniProtKB/TrEMBL
  A0A8I6AGM8_RAT UniProtKB/TrEMBL
  A0A8I6AHV0_RAT UniProtKB/TrEMBL
  A0A8I6AJ46_RAT UniProtKB/TrEMBL
  A0A8I6AMP8 ENTREZGENE, UniProtKB/TrEMBL
  A0A8L2QK62 ENTREZGENE, UniProtKB/TrEMBL
  A6JZ64_RAT UniProtKB/TrEMBL
  A6JZ65_RAT UniProtKB/TrEMBL
  A6JZ66 ENTREZGENE, UniProtKB/TrEMBL
  A6JZ67_RAT UniProtKB/TrEMBL
  PMGT1_RAT UniProtKB/Swiss-Prot, ENTREZGENE
1 to 36 of 36 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2013-08-14 Pomgnt1  protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)  Pomgnt1  protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2006-03-30 Pomgnt1  protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase  MGC94463  O-linked mannose beta1,2-N-acetylglucosaminyltransferase  Symbol and Name updated 1299863 APPROVED
2005-07-29 MGC94463  O-linked mannose beta1,2-N-acetylglucosaminyltransferase      Symbol and Name status set to provisional 70820 PROVISIONAL