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Gene Gene information from NCBI Gene database.
Entrez ID 4958
Gene name Osteomodulin
Gene symbol OMD
Synonyms (NCBI Gene)
OSADSLRR2C
Chromosome 9
Chromosome location 9q22.31
miRNA miRNA information provided by mirtarbase database.
66 Show/Hide all (66)
miRTarBase ID miRNA Experiments Reference
MIRT662854 hsa-miR-5197-5p HITS-CLIP 23824327
MIRT662853 hsa-miR-130a-3p HITS-CLIP 23824327
MIRT662852 hsa-miR-130b-3p HITS-CLIP 23824327
MIRT662851 hsa-miR-301a-3p HITS-CLIP 23824327
MIRT662850 hsa-miR-301b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8 Show/Hide all (8)
GO ID Ontology Definition Evidence Reference
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region TAS
GO:0005615 Component Extracellular space IBA
GO:0005796 Component Golgi lumen TAS
GO:0007155 Process Cell adhesion IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618926 8134 ENSG00000127083
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99983
Protein name Osteomodulin (Keratan sulfate proteoglycan osteomodulin) (KSPG osteomodulin) (Osteoadherin) (OSAD)
Protein function May be implicated in biomineralization processes. Has a function in binding of osteoblasts via the alpha(V)beta(3)-integrin.
PDB 5YQ5
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13855 LRR_8 92 → 153 Leucine rich repeat Repeat
PF13855 LRR_8 233 → 292 Leucine rich repeat Repeat
Tissue specificity TISSUE SPECIFICITY: Bone specific.
Sequence
MGFLSPIYVIFFFFGVKVHCQYETYQWDEDYDQEPDDDYQTGFPFRQNVDYGVPFHQYTL
GCVSECFCPTNFPSSMYCDNRKLKTIPNIPMHIQQLYLQFNEIEAVTANSFINATHLKEI
NLSHNKIKSQKIDYGVFAKLPNLLQLHLEHNNL
EEFPFPLPKSLERLLLGYNEISKLQTN
AMDGLVNLTMLDLCYNYLHDSLLKDKIFAKMEKLMQLNLCSNRLESMPPGLPSSLMYLSL
ENNSISSIPEKYFDKLPKLHTLRMSHNKLQDIPYNIFNLPNIVELSVGHNKL
KQAFYIPR
NLEHLYLQNNEIEKMNLTVMCPSIDPLHYHHLTYIRVDQNKLKEPISSYIFFCFPHIHTI
YYGEQRSTNGQTIQLKTQVFRRFPDDDDESEDHDDPDNAHESPEQEGAEGHFDLHYYENQ
E
Sequence length 421
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Reactome Pathway
Keratan sulfate biosynthesis
Keratan sulfate degradation
Defective CHST6 causes MCDC1
Defective ST3GAL3 causes MCT12 and EIEE15
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)