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NR1H4

nuclear receptor subfamily 1 group H member 4

HCNC Approved Symbol
NR1H4 (HGNC:7967)
Genomic Coordinates
12:100,473,866 - 100,564,414 (12q23.1)
Synonyms
FXR, RIP14, HRR1, HRR-1
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the NR1H4 gene.

Frequently observed phenotypes

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

No Results
NR1H4 - Gene browser | 3billion