Protein O-glucosyltransferase 1

Summary
UniProt ID
Q8NBL1
Gene Symbol
  • POGLUT1
  • C3orf9
  • CLP46
  • KTELC1
  • MDSRP
Organism
Homo sapiens (human)
External Links
GlycoProtDB
GPDB0015785
GlyConnect
GlyGen
Q8NBL1
PubChem
Q8NBL1
The O-GlcNAc Database
Q8NBL1
O-GlcNAcAtlas
Q8NBL1
Annotation
Keyword
  • 3D-structure
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Endoplasmic reticulum
  • Gastrulation
  • Glycoprotein
  • Glycosyltransferase
  • Limb-girdle muscular dystrophy
  • Reference proteome
  • Signal
Gene Ontology (GO)
Sequence
MEWWASSPLRLWLLLFLLPSAQGRQKESGSKWKVFIDQINRSLENYEPCSSQNCSCYHGVIEEDLTPFRGGISRKMMAEVVRRKLGTHYQITKNRLYRENDCMFPSRCSGVEHFILEVIGRLPDMEMVINVRDYPQVPKWMEPAIPVFSFSKTSEYHDIMYPAWTFWEGGPAVWPIYPTGLGRWDLFREDLVRSAAQWPWKKKNSTAYFRGSRTSPERDPLILLSRKNPKLVDAEYTKNQAWKSMKDTLGKPAAKDVHLVDHCKYKYLFNFRGVAASFRFKHLFLCGSLVFHVGDEWLEFFYPQLKPWVHYIPVKTDLSNVQELLQFVKANDDVAQEIAERGSQFIRNHLQMDDITCYWENLLSEYSKFLSYNVTRRKGYDQIIPKMLKTEL
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
373
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Pre-NOTCH Processing in the Endoplasmic Reticulum Homo sapiens
Disease
Displaying entries 31 - 40 of 68 in total
DO ID Disease Name Source
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M
DOID:0110297 autosomal recessive limb-girdle muscular dystrophy type 2K
DOID:0110298 autosomal recessive limb-girdle muscular dystrophy type 2N
DOID:0110299 autosomal recessive limb-girdle muscular dystrophy type 2I
DOID:0110300 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A
DOID:0110301 obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
DOID:0110302 obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
DOID:0110303 autosomal dominant limb-girdle muscular dystrophy type 1H
DOID:0110304 autosomal dominant limb-girdle muscular dystrophy type 2
DOID:0110305 autosomal dominant limb-girdle muscular dystrophy type 1

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024