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PROKR2

prokineticin receptor 2

HCNC Approved Symbol
PROKR2 (HGNC:15836)
Genomic Coordinates
20:5,299,218 - 5,316,954 (20p12.3)
Synonyms
GPR73b, PKR2, GPRg2, dJ680N4.3, GPR73L1, KAL3
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 PROKR2 gene.

Frequently observed phenotypes

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

Micropenis
 2 (100.0%)
Bilateral cleft lip and palate
 1 (50.0%)
Chronic kidney disease
 1 (50.0%)
Cryptorchidism
 1 (50.0%)
Gastroesophageal reflux disease
 1 (50.0%)
PROKR2 - Gene browser | 3billion