TSPYL [Homo sapiens]

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Sudden infant death with dysgenesis of the testes syndrome in a non-Amish infant: A case report. [Am J Med Genet A. 2020]
Sudden infant death with dysgenesis of the testes syndrome in a non-Amish infant: A case report.
Slater B, Glinton K, Dai H, Lay E, Karaviti L, Mizerik E, Murali CN, Lalani SR, Bacino CA, Rossetti LZ. Am J Med Genet A. 2020 Nov; 182(11):2751-2754. Epub 2020 Sep 4.
Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland. [Mol Cell Probes. 2015]
Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland.
Schubert S, Haas C, Bartsch C, Mirshekarnejad M, Kohrs S, Roettinger I, Grosshennig A, Stuhrmann M, Scholz C, Schmidtke J. Mol Cell Probes. 2015 Feb; 29(1):31-4. Epub 2014 Nov 4.
Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility? [Fertil Steril. 2012]
Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?
Javaher P, Stuhrmann M, Wilke C, Frenzel E, Manukjan G, Grosshenig A, Dechend F, Schwaab E, Schmidtke J, Schubert S. Fertil Steril. 2012 Feb; 97(2):402-6. Epub 2011 Dec 2.

RefSeq genomic sequence
See the genomic reference sequence for the TSPYL1 gene (NG_033266.4).
RefSeq genomic sequence
See the genomic reference sequence for the TSPYL1 gene (NG_016217.1).
RefSeq protein
See the reference protein sequence for testis-specific Y-encoded-like protein 1 (NP_003300.1).

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Protein