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TSHB

thyroid stimulating hormone subunit beta

HCNC Approved Symbol
TSHB (HGNC:12372)
Genomic Coordinates
1:115,029,826 - 115,034,309 (1p13.2)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the TSHB gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Central hypothyroidism
 1 (100.0%)
Hypocortisolism
 1 (100.0%)
TSHB - Gene browser | 3billion