Homo sapiens Protein: SMOC2 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-99200.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SMOC2 | ||||||||||||||||||
Protein Name | SPARC related modular calcium binding 2 | ||||||||||||||||||
Synonyms | |||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000346537 | ||||||||||||||||||
InnateDB Gene | IDBG-99198 (SMOC2) | ||||||||||||||||||
Protein Structure | |||||||||||||||||||
UniProt Annotation | |||||||||||||||||||
Function | Promotes matrix assembly and cell adhesiveness (By similarity). Can stimulate endothelial cell proliferation, migration, as well as angiogenesis. {ECO:0000250, ECO:0000269PubMed:16774925}. | ||||||||||||||||||
Subcellular Localization | Secreted, extracellular space, extracellular matrix, basement membrane {ECO:0000250}. | ||||||||||||||||||
Disease Associations | Dentin dysplasia 1 (DTDP1) [MIM:125400]: A dental defect in which both primary and secondary dentitions are affected. The clinical crowns of both permanent and deciduous teeth are of normal shape, form and color in most cases, although they may be slightly opalescent and blue or brown. Teeth may be very mobile and exfoliate spontaneously because of inadequate root formation. On radiographs, the roots are short and may be more pointed than normal. Pulp chambers are usually absent except for a chevron- shaped remnant in the crown. Root canals are usually absent. {ECO:0000269PubMed:22152679}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | |||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000716
Thyroglobulin type-1 IPR002048 EF-hand domain IPR002350 Kazal domain IPR019577 SPARC/Testican, calcium-binding domain |
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PFAM |
PF00086
PF00036 PF13202 PF13405 PF00050 PF07648 PF10591 |
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PRINTS | |||||||||||||||||||
PIRSF | |||||||||||||||||||
SMART |
SM00211
SM00054 SM00280 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q9H3U7 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q9H3U7 | ||||||||||||||||||
TrEMBL | B4DNB1 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 64094 | ||||||||||||||||||
UniGene | Hs.487200 | ||||||||||||||||||
RefSeq | NP_071421 | ||||||||||||||||||
HUGO | HGNC:20323 | ||||||||||||||||||
OMIM | 607223 | ||||||||||||||||||
CCDS | CCDS5307 | ||||||||||||||||||
HPRD | 06244 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB014730 AB014737 AF173892 AJ249902 AK056700 AK297839 AK315920 AL109940 AL136099 AL138918 AL442124 AL832303 BC028420 BC047583 CH471051 | ||||||||||||||||||
GenPept | AAH28420 AAH47583 AAQ13639 BAB20267 BAB20274 BAG51789 BAG60173 BAH14291 CAC10353 CAI20434 CAI20435 CAI46175 EAW47462 | ||||||||||||||||||