Aliases: TEL.
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 |
|---|---|---|
| Fibrosarcoma | somatic driver somatic | |
| Ewing Sarcoma | no genetic record |
mechanism: ETV6 GGAA Counter-Regulation
discussion: (unnamed)
|
| Mixed Phenotype Acute Leukemia | no genetic record |
mechanism: Immature T-Lineage Program with Retained Myeloid Potential
|
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 |
|---|---|---|---|
| thrombocytopenia 5 MONDO:0014536 | AD | Definitive 2020-01-22 |
no dismech entry |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.