OMD

Gene Information
 
Gene Symbol
OMD
 
Aliases
OSAD, SLRR2C
 
Entrez Gene ID
 
Gene Name
Osteomodulin
 
Chromosomal Location
9q22.31
 
HGNC ID
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0070062 Cellular component Extracellular exosome HDA 23533145
Protein Information
 
Protein Name
Osteomodulin, KSPG osteomodulin, keratan sulfate proteoglycan osteomodulin, osteoadherin proteoglycan
 
Function
May be implicated in biomineralization processes. Has a function in binding of osteoblasts via the alpha(V)beta(3)-integrin (By similarity).
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF13855 LRR_8
Pathways
 
Reactome
 

 

Keratan sulfate biosynthesis
Keratan sulfate degradation
Defective CHST6 causes MCDC1
Defective ST3GAL3 causes MCT12 and EIEE15
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)

Interactions
 
STRING MINT IntAct
ENSP00000359380 O00767 O00767
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Endocrine System Diseases
PCOS
Musculoskeletal Diseases
Arthritis
References
 

Abnormal gene expression profiles in human ovaries from polycystic ovary syndrome patients.

Jansen Erik, Laven Joop S E, Dommerholt Henri B R, Polman Jan, van Rijt Cindy, van den Hurk Caroline, Westland Jolanda, Mosselman Sietse, Fauser Bart C J M
Global Business Inteligence Center, NV Organon, PO Box 20, 5340 BH Oss, The Netherlands. erik.jansen@organon.com
Mol Endocrinol. 2004 Dec;18(12):3050-63. doi: 10.1210/me.2004-0074. Epub 2004 Aug

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