Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Thyrotropin releasing hormone (TRH)

The TRH gene encodes thyrotropin releasing hormone, mutations of which cause hypothalamic hypothyreosis.

Genetests:

Clinic Method Carrier testing
Turnaround 5 days
Specimen type genomic DNA
Research Method Genomic sequencing of the entire coding region
Turnaround 25 days
Specimen type genomic DNA

Related Diseases:

Thyrotropin-releasing hormone deficiency
TRH

References:

1.

Krashes MJ et al. (2014) An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger.

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2.

Yamada M et al. (1991) Assignment of human preprothyrotropin-releasing hormone (TRH) gene to chromosome 3.

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3.

Yamada M et al. (1990) Cloning and structure of human genomic DNA and hypothalamic cDNA encoding human prepro thyrotropin-releasing hormone.

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4.

Roller ML et al. (1995) Localization of the thyrotropin-releasing hormone gene, Trh, on mouse chromosome 6.

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5.

Yamada M et al. (1999) Assignment of the thyrotropin-releasing hormone gene (TRH) to human chromosome 3q13.3-->q21 by in situ hybridization.

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6.

Gáspár E et al. (2010) Thyrotropin releasing hormone (TRH): a new player in human hair-growth control.

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7.

NCBI article

NCBI 7200 external link
8.

OMIM.ORG article

Omim 613879 external link
9.

Orphanet article

Orphanet ID 120259 external link
10.

Wikipedia article

Wikipedia EN (Thyrotropin-releasing_hormone) external link
Update: Aug. 14, 2020
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