Homo sapiens Gene: TSPEAR
Summary
InnateDB Gene IDBG-5364.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol TSPEAR
Gene Name thrombospondin-type laminin G domain and EAR repeats
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000175894
Encoded Proteins
thrombospondin-type laminin G domain and EAR repeats
thrombospondin-type laminin G domain and EAR repeats
thrombospondin-type laminin G domain and EAR repeats
thrombospondin-type laminin G domain and EAR repeats
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
Gene Information
Type Protein coding
Genomic Location Chromosome 21:44497892-44711580
Strand Reverse strand
Band q22.3
Transcripts
ENST00000323084 ENSP00000321987
ENST00000397916 ENSP00000381012
ENST00000614657 ENSP00000482422
ENST00000613245 ENSP00000478010
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
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Hs.660703
RefSeq NM_001272037 NM_144991 XM_005261157
HUGO
OMIM
CCDS CCDS13712 CCDS74801
HPRD 09845
IMGT
EMBL
GenPept
RNA Seq Atlas