Aliases: FLI, FLIL, Fli1, MGC39265.
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 |
|---|---|---|
| Dilated Cardiomyopathy |
untyped
Pathogenic Variants
|
mechanism: Sarcomeric and Cytoskeletal Dysfunction
|
| Dilated Cardiomyopathy 2J |
untyped
germline
partial loss of function
CLINGEN: moderate
|
mechanism: Biallelic FLII Variants; Reduced Flightless-I Function in Cardiomyocytes
|
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 |
|---|---|---|---|
| cardiomyopathy, dilated, 2j MONDO:0957984 | AR | Moderate 2026-03-04 |
Dilated Cardiomyopathy 2J
untyped
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.