Homo sapiens Protein: GPM6B
Summary
InnateDB Protein IDBP-45294.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GPM6B
Protein Name glycoprotein M6B
Synonyms M6B;
Species Homo sapiens
Ensembl Protein ENSP00000349420
InnateDB Gene IDBG-45290 (GPM6B)
Protein Structure
UniProt Annotation
Function May be involved in neural development. Involved in regulation of osteoblast function and bone formation. Involved in matrix vesicle release by osteoblasts; this function seems to involve maintenance of the actin cytoskeleton. May be involved in cellular trafficking of SERT and thereby in regulation of serotonin uptake. {ECO:0000269PubMed:21638316}.
Subcellular Localization Cell membrane {ECO:0000250}; Multi-pass membrane protein {ECO:0000250}. Note=Colocalizes with SERT at the plasma membrane. {ECO:0000250}.
Disease Associations
Tissue Specificity Neurons and glia; cerebellar Bergmann glia, in glia within white matter tracts of the cerebellum and cerebrum, and in embryonic dorsal root ganglia.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0001503 ossification
GO:0007399 nervous system development
GO:0015031 protein transport
GO:0030154 cell differentiation
GO:0030501 positive regulation of bone mineralization
GO:0032956 regulation of actin cytoskeleton organization
GO:0051612 negative regulation of serotonin uptake
GO:0051893 regulation of focal adhesion assembly
GO:0085029 extracellular matrix assembly
GO:2000009 negative regulation of protein localization to cell surface
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
GO:0045121 membrane raft
Protein Structure and Domains
PDB ID
InterPro IPR001614 Myelin proteolipid protein PLP
PFAM PF01275
PRINTS PR00214
PIRSF
SMART SM00002
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q13491
PhosphoSite PhosphoSite-
TrEMBL C9JZE8
UniProt Splice Variant
Entrez Gene 2824
UniGene Hs.732644
RefSeq NP_005269
HUGO HGNC:4461
OMIM 300051
CCDS CCDS14158
HPRD 02082
IMGT
EMBL AC003035 AC003037 AF016004 AF037340 AF037341 AF037342 AF037343 AF037344 AF037345 AF037346 AF037347 AF047191 AF047192 AF047193 AF047194 AF047195 AF047196 AF047197 AK095657 AK294314 BC008151 BC047295 CH471074 U45955
GenPept AAB16888 AAC19165 AAC19166 AAC28560 AAD13718 AAH08151 AAH47295 BAC04600 BAH11734 EAW98843 EAW98845 EAW98846 EAW98848