PROKR1

prokineticin receptor 1
OMIM: 607122, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green PROKR1 in Paediatric pseudo-obstruction syndrome


Level 2: Gastrohepatology
Version 2.5
Latest signed off version: v2.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Hirschsprung disease, MONDO:0018309
Tags
  • gene-checked