Normal function · from ai-gene-review (Q9UM73, commit 79fe13b38970) · AI-generated, not KB evidence

ai-gene-review has this gene at status DRAFT; the description is shown only once the review is complete. Read the draft upstream.

In the knowledge base · computed from kb/ at build time

Disorders

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.

DisorderRelationshipWhere the gene appears
ALK-Rearranged Non-Small Cell Lung Cancer somatic driver somatic
mechanism: ALK fusion oncoprotein formation; ALK kinase-domain mutation-mediated resistance
Anaplastic Large Cell Lymphoma somatic driver somatic
mechanism: ALK-Driven STAT3 Activation; Constitutive ALK Fusion Kinase Activity
animal model: Mus musculus
scoped to subtype: Systemic ALK-Positive
Inflammatory Myofibroblastic Tumor untyped
Causal somatic gene rearrangement
Malignant Peritoneal Mesothelioma untyped
Rare Recurrent Rearrangement
subtype: ALK-Rearranged
scoped to subtype: ALK-Rearranged
Neuroblastoma untyped
Oncogenic Driver Mutations
Non-Small Cell Lung Cancer untyped
Gene Rearrangements
ClinGen gene–disease validity · snapshot 2026-10-03 · matched to entries by MONDO

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 diseaseMOIClassificationdismech entry
neuroblastoma, susceptibility to, 3 MONDO:0013083 AD Definitive
2022-12-30
no dismech entry
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.