RecName: Full=F-box-like/WD repeat-containing protein TBL1X; AltName: - Protein

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Central Hypothyroidism and Novel Clinical Phenotypes in Hemizygous Truncation of TBL1X. [J Endocr Soc. 2019]
Central Hypothyroidism and Novel Clinical Phenotypes in Hemizygous Truncation of TBL1X.
García M, Barreda-Bonis AC, Jiménez P, Rabanal I, Ortiz A, Vallespín E, Del Pozo Á, Martínez-San Millán J, González-Casado I, Moreno JC. J Endocr Soc. 2019 Jan 1; 3(1):119-128. Epub 2018 Nov 23.
Mutations in TBL1X Are Associated With Central Hypothyroidism. [J Clin Endocrinol Metab. 2016]
Mutations in TBL1X Are Associated With Central Hypothyroidism.
Heinen CA, Losekoot M, Sun Y, Watson PJ, Fairall L, Joustra SD, Zwaveling-Soonawala N, Oostdijk W, van den Akker EL, Alders M, et al. J Clin Endocrinol Metab. 2016 Dec; 101(12):4564-4573. Epub 2016 Sep 7.
Further Delineation of Central Congenital Hypothyroidism due to Variants in TBL1X and IRS4. [Thyroid. 2023]
Further Delineation of Central Congenital Hypothyroidism due to Variants in TBL1X and IRS4.
Lauffer P, Naafs JC, Bikker H, Garrelfs MR, Mooij CF, Boelen A, Zwaveling-Soonawala N, van Trotsenburg ASP. Thyroid. 2023 Jul; 33(7):880-884. Epub 2023 Jun 20.

RefSeq genomic sequence
See the genomic reference sequence for the TBL1X gene (NG_053005.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the TBL1X gene.

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O60907 [Domain Mapping of Disease Mut...]
O60907
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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PANTHER Classification System
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reagents [ExactAntigen/Labome]
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Protein