PROKR1

prokineticin receptor 1
OMIM: 607122, Gene2Phenotype

1 panel

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


Version 1.5
Latest signed off version: v1.0 (22 Mar 2023)

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