thyrotropin subunit beta isoform 1 precursor [Homo sapiens]

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TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews. [Eur Thyroid J. 2022]
TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews.
Shaki D, Eskin-Schwartz M, Hadar N, Bosin E, Carmon L, Refetoff S, Hershkovitz E, Birk OS, Haim A. Eur Thyroid J. 2022 Jan 7; 11(1). Epub 2022 Jan 7.
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ. [Horm Res Paediatr. 2019]
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ.
Ebrhim RS, Bruellman RJ, Watanabe Y, Creech MK, Abdullah MA, Dumitrescu AM, Refetoff S, Weiss RE. Horm Res Paediatr. 2019; 92(6):390-394. Epub 2020 Jan 8.
A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. [Rev Paul Pediatr. 2019]
A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING.
Borges MF, Domené HM, Scaglia PA, Lara BHJ, Palhares HMDC, Santos AVA, Gonçalves ALF, Oliveira MM, Marqui ABT. Rev Paul Pediatr. 2019; 37(4):520-524. Epub 2019 Jun 3.

RefSeq genomic sequence
See the genomic reference sequence for the TSHB gene (NG_015891.1).
RefSeq mRNA
See reference mRNA sequence for the TSHB gene (NM_000549.5).
RefSeq protein isoforms
See the other reference sequence protein isoform for the TSHB gene (NP_001264920.1).

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NP_000540 [Domain Mapping of Disease Mut...]
NP_000540
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
OncoMX cancer biomarker resource [OncoMX cancer biomarker resou...]
OncoMX cancer biomarker resource
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Transcript/Protein Information
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reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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