POGLUT1 - 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
Autosomal Recessive Limb-Girdle Muscular Dystrophy	causative	mechanism: Reduced Notch Signalling in Muscle Progenitors subtype: LGMD2Z scoped to subtype: LGMD2Z
Dowling-Degos Disease	causative	mechanism: Notch Pathway Glycosylation and Cleavage Deficiency subtype: DDD4 scoped to subtype: DDD4

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
autosomal recessive limb-girdle muscular dystrophy MONDO:0015152	AR	Definitive 2024-08-14	Autosomal Recessive Limb-Girdle Muscular Dystrophy causative

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