Glycogenin-2

Summary
UniProt ID
O15488
Gene Symbol
  • GYG2
Organism
Homo sapiens (human)
External Links
GlyGen
O15488
PubChem
O15488
The Human Metabolome Database
HMDBP01095
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Glycogen biosynthesis
  • Glycoprotein
  • Manganese
  • Metal-binding
  • Phosphoprotein
  • Reference proteome
  • Transferase
Gene Ontology (GO)
Sequence
MSETEFHHGAQAGLELLRSSNSPTSASQSAGMTVTDQAFVTLATNDIYCQGALVLGQSLRRHRLTRKLVVLITPQVSSLLRVILSKVFDEVIEVNLIDSADYIHLAFLKRPELGLTLTKLHCWTLTHYSKCVFLDADTLVLSNVDELFDRGEFSAAPDPGWPDCFNSGVFVFQPSLHTHKLLLQHAMEHGSFDGADQGLLNSFFRNWSTTDIHKHLPFIYNLSSNTMYTYSPAFKQFGSSAKVVHFLGSMKPWNYKYNPQSGSVLEQGSASSSQHQAAFLHLWWTVYQNNVLPLYKSVQAGEARASPGHTLCHSDVGGPCADSASGVGEPCENSTPSAGVPCANSPLGSNQPAQGLPEPTQIVDETLSLPEGRRSEDMIACPETETPAVITCDPLSQPSPQPADFTETETILQPANKVESVSSEETFEPSQELPAEALRDPSLQDALEVDLAVSVSQISIEEKVKELSPEEERRKWEEGRIDYMGKDAFARIQEKLDRFLQ
Glycosylation Sites
Displaying 1 entry
Position Description PubMed ID GlyTouCan ID Source
228 O-linked (Glc...) tyrosine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 4 entries
Pathway Name Organism
GSD 0 Homo sapiens
GSD IV Homo sapiens
Glycogen breakdown (glycogenolysis) Homo sapiens
Glycogen synthesis Homo sapiens
Disease
Displaying all 10 entries
DO ID Disease Name Source
DOID:0111040 glycogen storage disease IXd
DOID:0111041 glycogen storage disease IXb
DOID:0111042 glycogen storage disease IXa
DOID:0111043 glycogen storage disease IXc
DOID:2747 glycogen storage disease
DOID:2749 glycogen storage disease Ia
DOID:2862 glucosephosphate dehydrogenase deficiency
DOID:3652 Leigh disease
DOID:9266 cystinuria
DOID:9870 galactosemia

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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