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RORA

RAR related orphan receptor A

HCNC Approved Symbol
RORA (HGNC:10258)
Genomic Coordinates
15:60,488,284 - 61,229,302 (15q22.2)
Synonyms
RZRA, ROR1, ROR2, ROR3, NR1F1, ROR-alpha, RORalpha, RORa1, RORα
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the RORA gene.

Frequently observed phenotypes

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

Ataxia
 1 (50.0%)
Global developmental delay
 1 (50.0%)
Epilepsia partialis continua
 1 (50.0%)
RORA - Gene browser | 3billion