Homo sapiens Protein: ODZ3
Summary
InnateDB Protein IDBP-480886.4
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ODZ3
Protein Name odz, odd Oz/ten-m homolog 3 (Drosophila)
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000424226
InnateDB Gene IDBG-281665 (ODZ3)
Protein Structure
UniProt Annotation
Function Involved in neural development, regulating the establishment of proper connectivity within the nervous system. Promotes axon guidance and homophilic cell adhesion. Plays a role in the development of the visual pathway; regulates the formation in ipsilateral retinal mapping to both the dorsal lateral geniculate nucleus (dLGN) and the superior colliculus (SC). May be involved in the differentiation of the fibroblast-like cells in the superficial layer of mandibular condylar cartilage into chondrocytes. May function as a cellular signal transducer (By similarity). {ECO:0000250}.
Subcellular Localization Membrane {ECO:0000305}; Single-pass membrane protein {ECO:0000305}. Cell projection, axon {ECO:0000250}.
Disease Associations Microphthalmia, isolated, with coloboma, 9 (MCOPCB9) [MIM:615145]: A disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues. Ocular abnormalities like opacities of the cornea and lens, scaring of the retina and choroid, and other abnormalities may also be present. Ocular colobomas are a set of malformations resulting from abnormal morphogenesis of the optic cup and stalk, and the fusion of the fetal fissure (optic fissure). {ECO:0000269PubMed:22766609}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed in adult and fetal brain, slightly lower levels in testis and ovary, and intermediate levels in all other peripheral tissues examined. Not expressed in spleen or liver. Expression was high in brain, with highest levels in amygdala and caudate nucleus, followed by thalamus and subthalamic nucleus. {ECO:0000269PubMed:10625539, ECO:0000269PubMed:10819331}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0009055 electron carrier activity
GO:0020037 heme binding
GO:0042803 protein homodimerization activity
GO:0046982 protein heterodimerization activity
Biological Process
GO:0007156 homophilic cell adhesion
GO:0007165 signal transduction
GO:0010976 positive regulation of neuron projection development
GO:0048593 camera-type eye morphogenesis
GO:0097264 self proteolysis
Cellular Component
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0030424 axon
Protein Structure and Domains
PDB ID
InterPro IPR000742 Epidermal growth factor-like domain
IPR006530 YD repeat
IPR008969 Carboxypeptidase-like, regulatory domain
IPR009056 Cytochrome c-like domain
IPR009471 Teneurin intracellular, N-terminal
IPR013111 EGF-like domain, extracellular
IPR022385 Rhs repeat-associated core
PFAM PF00008
PF05593
PF13442
PF06484
PF07974
PRINTS
PIRSF
SMART SM00181
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9P273
PhosphoSite PhosphoSite-Q9P273
TrEMBL G3CAS9
UniProt Splice Variant
Entrez Gene 55714
UniGene Hs.130438
RefSeq NP_001073946
HUGO HGNC:29944
OMIM 610083
CCDS CCDS47165
HPRD
IMGT
EMBL AB040888 AC079226 AC093601 AC105288 AC108142 AC109353 AC131943 AF195420 AK001336 AK001748 AK027473 AY736855 HE578284
GenPept AAF28318 AAU84915 BAA91633 BAA91879 BAA95979 BAB55138 CCD17868