SLC6A4 - dismech genes

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.

Disorder	Relationship	Where the gene appears
Dissociative Identity Disorder	susceptibility germline
Fibromyalgia	untyped Risk Factor
Generalized Anxiety Disorder	untyped Risk Factor
Major Depressive Disorder	untyped Risk Factor
Cocaine Intoxication	no genetic record	mechanism: Monoamine Transporter Blockade

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 disease	MOI	Classification	dismech entry
autism spectrum disorder MONDO:0005258	AD	Disputed 2021-01-06	Autism Spectrum Disorder not named

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