Keratocan

Summary
UniProt ID
O60938
Gene Symbol
KERA SLRR2B
Gene ID
11081
Organism
Homo sapiens (human)
GlyConnect
GlyGen
O60938
The Human Metabolome Database
HMDBP02315
The O-GlcNAc Database
O60938
O-GlcNAcAtlas
O60938
Re-Glyco
O60938
Sequence
MAGTICFIMWVLFITDTVWSRSVRQVYEVHDSDDWTIHDFECPMECFCPPSFPTALYCENRGLKEIPAIPSRIWYLYLQNNLIETIPEKPFENATQLRWINLNKNKITNYGIEKGALSQLKKLLFLFLEDNELEEVPSPLPRSLEQLQLARNKVSRIPQGTFSNLENLTLLDLQNNKLVDNAFQRDTFKGLKNLMQLNMAKNALRNMPPRLPANTMQLFLDNNSIEGIPENYFNVIPKVAFLRLNHNKLSDEGLPSRGFDVSSILDLQLSHNQLTKVPRISAHLQHLHLDHNKIKSVNVSVICPSPSMLPAERDSFSYGPHLRYLRLDGNEIKPPIPMALMTCFRLLQAVII
Glycosylation Sites
Displaying all 5 entries
Position Description PubMed ID GlyTouCan ID Source
71
93
  • N-linked (GlcNAc...) (keratan sulfate) asparagine
167
  • N-linked (GlcNAc...) (keratan sulfate) asparagine
222
  • N-linked (GlcNAc...) asparagine
298
  • N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 5 entries
Pathway Name Organism
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Homo sapiens
Defective CHST6 causes MCDC1 Homo sapiens
Defective ST3GAL3 causes MCT12 and EIEE15 Homo sapiens
Keratan sulfate biosynthesis Homo sapiens
Keratan sulfate degradation Homo sapiens
Disease
Displaying all 3 entries
DO ID Disease Name Source
DOID:2566 corneal dystrophy
DOID:11342 arcus senilis
DOID:0060287 cornea plana

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: April 6, 2026