Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 7252
MIM: 188540
HGNC: 12372
Ensembl: ENSG00000134200
Variants:
dbSNP: 7252
ClinVar: 7252
TCGA: ENSG00000134200
COSMIC: TSHB
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000134200 | ENST00000256592 | P01222 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32242612 | 2020 | Cold Exposure Distinctively Modulates Parathyroid and Thyroid Hormones in Cold-Acclimatized and Non-Acclimatized Humans. | 10 |
| 32738139 | 2020 | The Human TSHβ Subunit Proteins and Their Binding Sites on the TSH Receptor Using Molecular Dynamics Simulation. | 1 |
| 32769997 | 2020 | GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. | 47 |
| 32242612 | 2020 | Cold Exposure Distinctively Modulates Parathyroid and Thyroid Hormones in Cold-Acclimatized and Non-Acclimatized Humans. | 10 |
| 32738139 | 2020 | The Human TSHβ Subunit Proteins and Their Binding Sites on the TSH Receptor Using Molecular Dynamics Simulation. | 1 |
| 32769997 | 2020 | GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. | 47 |
| 30940720 | 2019 | Thyrotropin aggravates atherosclerosis by promoting macrophage inflammation in plaques. | 6 |
| 31166470 | 2019 | A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. | 1 |
| 31703413 | 2019 | The Pathogenic TSH β-subunit Variant C105Vfs114X Causes a Modified Signaling Profile at TSHR. | 3 |
| 31914441 | 2019 | Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ. | 1 |
| 30940720 | 2019 | Thyrotropin aggravates atherosclerosis by promoting macrophage inflammation in plaques. | 6 |
| 31166470 | 2019 | A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING. | 1 |
| 31703413 | 2019 | The Pathogenic TSH β-subunit Variant C105Vfs114X Causes a Modified Signaling Profile at TSHR. | 3 |
| 31914441 | 2019 | Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβ. | 1 |
| 26898119 | 2017 | Serum cytokine profile in patients with breast cancer. | 17 |
Citation
Dessen P
TSHB (thyroid stimulating hormone subunit beta)
Atlas Genet Cytogenet Oncol Haematol. 2012-06-01
Online version: http://atlasgeneticsoncology.org/gene/52753/tshb
