Previous symbols: NRAMP2. Aliases: DCT1, DMT1, DMT-1, FLJ37416.
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 |
|---|---|---|
| Cadmium Poisoning | susceptibility | |
| Microcytic Anemia With Liver Iron Overload | causative |
mechanism: SLC11A2/DMT1 Loss of Function
|
| Manganism | no genetic record |
mechanism: Manganese Transport Across the Blood-Brain Barrier
|
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 |
|---|---|---|---|
| microcytic anemia with liver iron overload MONDO:0008787 | AR | Definitive 2025-04-25 |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.