Previous symbols: GPR73L1, KAL3. Aliases: GPR73b, PKR2, GPRg2, dJ680N4.3.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Kallmann Syndrome | causative |
mechanism: Defective GnRH neuron and olfactory axon migration
subtype: PROKR2_PROK2
scoped to subtype: PROKR2_PROK2
|
| Congenital Aural Atresia | no genetic record |
mechanism: Dysregulated PROKR2 Expression
|
| Ectopic Pregnancy | no genetic record |
mechanism: Aberrant Tubal Receptivity
|
An entry matches when ClinGen's MONDO disease is the entry's own disease term, a subtype term, or an exact-match mapping. An amber status marks an entry ClinGen supports the gene for (Definitive, Strong or Moderate) whose own record does not type it. A Limited, Disputed or Refuted tier on such an entry is not a gap.
| ClinGen disease | MOI | Classification | dismech entry |
|---|---|---|---|
| hypogonadotropic hypogonadism 3 with or without anosmia MONDO:0009482 | AD | Definitive 2022-04-26 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.