MEPE (matrix extracellular phosphoglycoprotein)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID 56955
Gene name Matrix extracellular phosphoglycoprotein
Gene symbol MEPE
Synonyms (NCBI Gene)
OF45
Chromosome 4
Chromosome location 4q22.1
Summary This gene encodes a secreted calcium-binding phosphoprotein that belongs to the small integrin-binding ligand, N-linked glycoprotein (SIBLING) family of proteins. Members of this family are components of the extracellular matrix of bone and dentin and reg
miRNA miRNA information provided by mirtarbase database.
14
Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Show/Hide all (14)
miRTarBase ID miRNA Experiments Reference
MIRT017419 hsa-miR-335-5p Microarray 18185580
MIRT022428 hsa-miR-124-3p Microarray 18668037
MIRT437788 hsa-miR-376a-3p HepG2" 23570370
MIRT2270420 hsa-miR-181a CLIP-seq
MIRT2270421 hsa-miR-181b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Show/Hide all (10)
GO ID Ontology Definition Evidence Reference
GO:0001501 Process Skeletal system development TAS 10945470
GO:0005201 Function Extracellular matrix structural constituent TAS 10945470
GO:0005515 Function Protein binding IPI 15664000, 17474147, 32296183
GO:0005576 Component Extracellular region IEA
GO:0005788 Component Endoplasmic reticulum lumen TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
MIM HGNC e!Ensembl
605912 13361 ENSG00000152595
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9NQ76
Protein name Matrix extracellular phosphoglycoprotein (Osteoblast/osteocyte factor 45) (OF45) (Osteoregulin)
Protein function Promotes renal phosphate excretion and inhibits intestinal phosphate absorption (PubMed:14962809, PubMed:19005008). Promotes bone mineralization by osteoblasts and cartilage mineralization by chondrocytes (PubMed:18162525, PubMed:19998030, PubMe
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07175 Osteoregulin 97 → 256 Osteoregulin Family
Tissue specificity TISSUE SPECIFICITY: Detected in urine (at protein level) (PubMed:37453717). Expressed by osteoblasts (PubMed:10945470, PubMed:11414762, PubMed:15108058). Expressed by stem cells in dental pulp (PubMed:15153459). Expressed by mesenchymal cells in dental pa
Sequence 
MRVFCVGLLLFSVTWAAPTFQPQTEKTKQSCVEEQRQEEKNKDNIGFHHLGKRINQELSS
KENIVQERKKDLSLSEASENKGSSKSQNYFTNRQRLNKEYSISNKENTHNGLRMSIYPKS
TGNKGFEDGDDAISKLHDQEEYGAALIRNNMQHIMGPVTAIKLLGEENKENTPRNVLNII
PASMNYAKAHSKDKKKPQRDSQAQKSPVKSKSTHRIQHNIDYLKHLSKVKKIPSDFEGSG
YTDLQERGDNDISPFSGDGQPFKDIPGKGEATGPDLEGKDIQTGFAGPSEAESTHLDTKK
PGYNEIPEREENGGNTIGTRDETAKEADAVDVSLVEGSNDIMGSTNFKELPGREGNRVDA
GSQNAHQGKVEFHYPPAPSKEKRKEGSSDAAESTNYNEIPKNGKGSTRKGVDHSNRNQAT
LNEKQRFPSKGKSQGLPIPSRGLDNEIKNEMDSFNGPSHENIITHGRKYHYVPHRQNNST
RNKGMPQGKGSWGRQPHSNRRFSSRRRDDSSESSDSGSSSESDGD
Sequence length 525
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
  KEGG  Reactome
  ECM-receptor interaction   Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Post-translational protein phosphorylation
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Gene miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Show/Hide Unknown Diseases (1)
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
MEPE-related disorder Uncertain significance; Likely benign; Benign rs201213159, rs113931822, rs200300679, rs754696980, rs2476174507, rs148637496, rs374783833, rs141911146, rs61731018, rs548626494, rs138665285, rs141864614, rs115322331, rs150454926, rs139311420
View all (8 more)		 RCV003918981
RCV004750861
RCV003393081
RCV003412149
RCV003404424
RCV003894635
RCV003921415
RCV003933936
RCV003941937
RCV003964087
RCV003941393
RCV003941591
RCV003922033
RCV003934220
RCV003934259
RCV003971629
RCV004750960
RCV003960585
RCV003913214
RCV003960586
RCV003978151
RCV003960587
RCV003913215
Show/Hide Text Mining Associations (26)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Bone Diseases Associate 17900349, 30287925
Bone Diseases Metabolic Associate 24747200
Cardiovascular Diseases Associate 21779381
Cerebral Infarction Associate 21779381
Chronic Kidney Disease Mineral and Bone Disorder Associate 33097703
Craniofacial Abnormalities Associate 30287925
Dental Plaque Associate 35535576
Dentin Dysplasia Associate 23451077
Epilepsy Associate 21779381
Facial paresis hereditary congenital Associate 30287925