Aliases: STK1, FLK2, CD135.
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 |
|---|---|---|
| Acute Myeloid Leukemia with CEBPA Somatic Mutations | modifier somatic |
scoped to subtype: CEBPA bZIP In-Frame-Indel AML
|
| Acute Promyelocytic Leukemia, PML-RARA | cooperating somatic |
mechanism: FLT3-ITD-Driven Proliferative Signaling
animal model: Mus musculus
|
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 |
|---|---|---|---|
| leukemia, acute myeloid, susceptibility to MONDO:0100173 | AD | Limited 2025-11-18 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.