Homo sapiens Protein: TSPEAR
Summary
InnateDB Protein IDBP-5368.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TSPEAR
Protein Name thrombospondin-type laminin G domain and EAR repeats
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000321987
InnateDB Gene IDBG-5364 (TSPEAR)
Protein Structure
UniProt Annotation
Function May play a role in development or function of the auditory system.
Subcellular Localization Secreted {ECO:0000250}. Cell surface {ECO:0000250}. Cell projection, stereocilium {ECO:0000250}. Note=Secreted protein which may bind to the cell surface via a membrane receptor. {ECO:0000250}.
Disease Associations Deafness, autosomal recessive, 98 (DFNB98) [MIM:614861]: A form of non-syndromic sensorineural hearing loss with prelingual onset. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. {ECO:0000269PubMed:22678063}. 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 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
Biological Process
GO:0007605 sensory perception of sound
Cellular Component
GO:0005576 extracellular region
GO:0009986 cell surface
GO:0032420 stereocilium
GO:0060170 ciliary membrane
Protein Structure and Domains
PDB ID
InterPro IPR001791 Laminin G domain
IPR005492 Leucine-rich glioma-inactivated , EPTP repeat
IPR008985 Concanavalin A-like lectin/glucanases superfamily
IPR009039 EAR
PFAM PF00054
PF02210
PF03736
PRINTS
PIRSF
SMART SM00210
SM00282
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8WU66
PhosphoSite PhosphoSite-Q8WU66
TrEMBL
UniProt Splice Variant
Entrez Gene 54084
UniGene Hs.660703
RefSeq NP_659428
HUGO HGNC:1268
OMIM 612920
CCDS CCDS13712
HPRD 09845
IMGT
EMBL AJ487962 BC021197
GenPept AAH21197 CAD32309