Fibromodulin

Summary
UniProt ID
Q06828
Gene Symbol
  • FMOD
  • FM
  • SLRR2E
Organism
Homo sapiens (human)
External Links
GlycoProtDB
GPDB0011800
GlyConnect
GlyGen
Q06828
PubChem
Q06828
The Human Metabolome Database
HMDBP02327
Annotation
Keyword
  • 3D-structure
  • Disulfide bond
  • Extracellular matrix
  • Leucine-rich repeat
  • Proteoglycan
  • Pyrrolidone carboxylic acid
  • Reference proteome
  • Repeat
  • Signal
  • Sulfation
Gene Ontology (GO)
Sequence
MQWTSLLLLAGLFSLSQAQYEDDPHWWFHYLRSQQSTYYDPYDPYPYETYEPYPYGVDEGPAYTYGSPSPPDPRDCPQECDCPPNFPTAMYCDNRNLKYLPFVPSRMKYVYFQNNQITSIQEGVFDNATGLLWIALHGNQITSDKVGRKVFSKLRHLERLYLDHNNLTRMPGPLPRSLRELHLDHNQISRVPNNALEGLENLTALYLQHNEIQEVGSSMRGLRSLILLDLSYNHLRKVPDGLPSALEQLYMEHNNVYTVPDSYFRGAPKLLYVRLSHNSLTNNGLASNTFNSSSLLELDLSYNQLQKIPPVNTNLENLYLQGNRINEFSISSFCTVVDVVNFSKLQVLRLDGNEIKRSAMPADAPLCLRLASLIEI
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
127
166
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying all 6 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
ECM proteoglycans Homo sapiens
Keratan sulfate biosynthesis Homo sapiens
Keratan sulfate degradation Homo sapiens
Disease
Displaying entries 21 - 30 of 62 in total
DO ID Disease Name Source
DOID:2348 arteriosclerotic cardiovascular disease
DOID:2349 arteriosclerosis
DOID:2527 nephrosis
DOID:2660 cystic teratoma
DOID:2921 glomerulonephritis
DOID:2964 periarthritis
DOID:3068 glioblastoma
DOID:3070 high grade glioma
DOID:3071 gliosarcoma
DOID:3074 giant cell glioblastoma

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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