Previous symbols: LENG4. Aliases: BB1, hMBOA-7, LPLAT, LPIAT1, LPLAT11.
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 Non-Syndromic Intellectual Disability | causative germline |
mechanism: Impaired Synaptic Transmission and Plasticity
subtype: MRT57
scoped to subtype: MRT57
|
| Metabolic Dysfunction-Associated Steatotic Liver Disease | susceptibility germline |
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 |
|---|---|---|---|
| complex neurodevelopmental disorder MONDO:0100038 | AR | Definitive 2023-11-21 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.