Homo sapiens thrombospondin type laminin G domain and EAR repeats (TSP - Nucleotide

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Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14. [HGG Adv. 2023]
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14.
Jackson A, Lin SJ, Jones EA, Chandler KE, Orr D, Moss C, Haider Z, Ryan G, Holden S, Harrison M, et al. HGG Adv. 2023 Apr 13; 4(2):100186. Epub 2023 Mar 3.
Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity. [Genes (Basel). 2022]
Confirmation of a Phenotypic Entity for TSPEAR Variants in Egyptian Ectodermal Dysplasia Patients and Role of Ethnicity.
Rabie EA, Sayed ISM, Amr K, Ahmed HA, Mostafa MI, Hassib NF, El-Sayed H, Zada SK, El-Kamah G. Genes (Basel). 2022 Jun 13; 13(6). Epub 2022 Jun 13.
TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study. [Am J Med Genet A. 2021]
TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study.
Bowles B, Ferrer A, Nishimura CJ, Pinto E Vairo F, Rey T, Leheup B, Sullivan J, Schoch K, Stong N, Agolini E, et al. Am J Med Genet A. 2021 Aug; 185(8):2417-2433. Epub 2021 May 27.

RefSeq alternative splicing
See the other reference mRNA sequence splice variant for the TSPEAR gene (NM_144991.3).

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Protein sequence from Nucleotide coding region
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Nucleotide