Aliases: LKLF.
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 |
|---|---|---|
| Splenic Marginal Zone Lymphoma | somatic driver somatic | |
| Hairy Cell Leukemia |
untyped
Recurrent cooperating mutation
|
|
| Marginal Zone Lymphoma | no genetic record |
mechanism: Deregulation of Marginal Zone B-Cell Differentiation Signalling
|
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 |
|---|---|---|---|
| pulmonary arterial hypertension MONDO:0015924 | AD | Limited 2022-11-03 |
Pulmonary_hypertension
not named
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.