Aliases: SLC55A1, Mdm38.
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 |
|---|---|---|
| LETM1-Related Childhood-Onset Neurodegeneration | causative germline | |
| Wolf-Hirschhorn_Syndrome | susceptibility |
mechanism: Candidate Multigene Neuronal-Communication Dysfunction; LETM1 Haploinsufficiency and Mitochondrial Ion Dyshomeostasis
animal model: Mus musculus; Rattus norvegicus
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.