Procollagen galactosyltransferase 1

Summary
UniProt ID
Q8NBJ5
Gene Symbol
  • COLGALT1
  • GLT25D1
Organism
Homo sapiens (human)
External Links
GlyConnect
GlyGen
Q8NBJ5
PubChem
Q8NBJ5
The Human Metabolome Database
HMDBP11757
The O-GlcNAc Database
Q8NBJ5
RaftProt
Q8NBJ5
Annotation
Keyword
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Glycosyltransferase
  • Reference proteome
  • Signal
Gene Ontology (GO)
Sequence
MAAAPRAGRRRGQPLLALLLLLLAPLPPGAPPGADAYFPEERWSPESPLQAPRVLIALLARNAAHALPTTLGALERLRHPRERTALWVATDHNMDNTSTVLREWLVAVKSLYHSVEWRPAEEPRSYPDEEGPKHWSDSRYEHVMKLRQAALKSARDMWADYILFVDADNLILNPDTLSLLIAENKTVVAPMLDSRAAYSNFWCGMTSQGYYKRTPAYIPIRKRDRRGCFAVPMVHSTFLIDLRKAASRNLAFYPPHPDYTWSFDDIIVFAFSCKQAEVQMYVCNKEEYGFLPVPLRAHSTLQDEAESFMHVQLEVMVKHPPAEPSRFISAPTKTPDKMGFDEVFMINLRRRQDRRERMLRALQAQEIECRLVEAVDGKAMNTSQVEALGIQMLPGYRDPYHGRPLTKGELGCFLSHYNIWKEVVDRGLQKSLVFEDDLRFEIFFKRRLMNLMRDVEREGLDWDLIYVGRKRMQVEHPEKAVPRVRNLVEADYSYWTLAYVISLQGARKLLAAEPLSKMLPVDEFLPVMFDKHPVSEYKAHFSLRNLHAFSVEPLLIYPTHYTGDDGYVSDTETSVVWNNEHVKTDWDRAKSQKMREQQALSREAKNSDVLQSPLDSAARDEL
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Collagen biosynthesis and modifying enzymes Homo sapiens
Disease
Displaying entries 1 - 10 of 14 in total
DO ID Disease Name Source
DOID:0060215 Balo concentric sclerosis
DOID:0060248 Simpson-Golabi-Behmel syndrome type 1
DOID:0060263 porencephaly
DOID:10588 adrenoleukodystrophy
DOID:11832 visual epilepsy
DOID:12697 locked-in syndrome
DOID:12835 quadriplegia
DOID:1443 cerebral degeneration
DOID:1826 epilepsy
DOID:331 central nervous system disease

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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