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

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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.
Novel TSPEAR mutations in non-syndromic oligodontia. [Oral Dis. 2020]
Novel TSPEAR mutations in non-syndromic oligodontia.
Song JS, Bae M, Kim JW. Oral Dis. 2020 May; 26(4):847-849. Epub 2020 Mar 19.

RefSeq genomic sequence
See the genomic reference sequence for the TSPEAR gene (NG_033806.2).
RefSeq mRNA
See reference mRNA sequence for the TSPEAR gene (NM_001272037.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the TSPEAR gene (NP_659428.2).

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NP_001258966 [Domain Mapping of Disease Mut...]
NP_001258966
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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