thrombospondin-type laminin G domain and EAR repeat-containing protein - Protein

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Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness. [Hum Mol Genet. 2012]
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness.
Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C. Hum Mol Genet. 2012 Sep 1; 21(17):3835-44. Epub 2012 Jun 7.
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis. [PLoS Genet. 2016]
Mutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.
Peled A, Sarig O, Samuelov L, Bertolini M, Ziv L, Weissglas-Volkov D, Eskin-Schwartz M, Adase CA, Malchin N, Bochner R, et al. PLoS Genet. 2016 Oct; 12(10):e1006369. Epub 2016 Oct 13.
The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders. [Trends Biochem Sci. 2002]
The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders.
Staub E, Pérez-Tur J, Siebert R, Nobile C, Moschonas NK, Deloukas P, Hinzmann B. Trends Biochem Sci. 2002 Sep; 27(9):441-4.

RefSeq protein isoforms
See 7 reference sequence protein isoforms for the Tspear gene.

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Protein