Homo sapiens Gene: OPTC
Summary
InnateDB Gene IDBG-105958.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol OPTC
Gene Name opticin
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000188770
Encoded Proteins
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Opticin belongs to class III of the small leucine-rich repeat protein (SLRP) family. Members of this family are typically associated with the extracellular matrix. Opticin is present in significant quantities in the vitreous of the eye and also localizes to the cornea, iris, ciliary body, optic nerve, choroid, retina, and fetal liver. Opticin may noncovalently bind collagen fibrils and regulate fibril morphology, spacing, and organization. The opticin gene is mapped to a region of chromosome 1 that is associated with the inherited eye diseases age-related macular degeneration (AMD) and posterior column ataxia with retinosa pigmentosa (AXPC1). [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 1:203494143-203508864
Strand Forward strand
Band q32.1
Transcripts
ENST00000367222 ENSP00000356191
ENST00000448911 ENSP00000399491
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0005201 extracellular matrix structural constituent
GO:0005515 protein binding
Biological Process
GO:0016525 negative regulation of angiogenesis
Cellular Component
GO:0005578 proteinaceous extracellular matrix
GO:0031012 extracellular matrix
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.632468
RefSeq NM_014359
HUGO
OMIM
CCDS CCDS1439
HPRD 05498
IMGT
EMBL
GenPept
RNA Seq Atlas