In the knowledge base ยท 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
Familial Visceral Neuropathy 2 causative germline loss of function
mechanism: Biallelic ERBB2 Kinase-Domain Variant
Gastric Adenocarcinoma somatic driver somatic
mechanism: Receptor Tyrosine Kinase Amplification
subtype: CIN
biochemical: HER2 (ERBB2) Overexpression or Amplification
scoped to subtype: CIN
Thymic Neuroendocrine Carcinoma biomarker somatic
Breast Carcinoma untyped
Amplification or overexpression
somatic
Cervical Adenocarcinoma untyped
Somatic Mutation / Amplification
Endometrial Carcinoma untyped
Somatic amplification or overexpression
scoped to subtype: Copy-Number High p53-Abnormal
Esophageal Adenocarcinoma untyped
Somatic Amplification
Esophageal Carcinoma untyped
Somatic Amplification
Ethmoid Sinus Adenocarcinoma untyped
Not amplified or overexpressed
Gallbladder Cancer untyped
Somatic Amplification/Activating Mutation
HER2-Positive Breast Cancer untyped
Somatic Amplification
Ovarian Mucinous Carcinoma untyped
HER2 gene amplification/overexpression in a targetable subset
BRAF V600E-Mutant Non-Small Cell Lung Cancer no genetic record
mechanism: MAPK Reactivation and Bypass Resistance
Small Intestine Cancer no genetic record
subtype: Adenocarcinoma
Vulvar Adenocarcinoma no genetic record
mechanism: HER2-Positive EMPD Signaling (Cross-Site Case Evidence)

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