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THRA

thyroid hormone receptor alpha

HCNC Approved Symbol
THRA (HGNC:11796)
Genomic Coordinates
17:40,062,193 - 40,093,867 (17q21.1)
Synonyms
EAR-7.1/EAR-7.2, THRA3, AR7, ERBA, NR1A1, TRalpha, TRalpha1, TRalpha2, c-ERBA-1, c-erbA, THRalpha, THRalpha1, THRalpha2, THRA1, THRA2, ERBA1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Hypothyroidism, congenital, nongoitrous, 6
614450AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the THRA gene.

Frequently observed phenotypes

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

No Results