Aliases: FLG1, FLG-1.
ai-gene-review has this gene at status unknown; the description is shown only once the review is complete. Read the draft upstream.
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 |
|---|---|---|
| Ichthyosis Vulgaris | causative germline loss of function |
mechanism: FLG Loss-of-Function Variants
subtype: Mild IV; Severe IV
|
| X-linked Reticulate Pigmentary Disorder | modifier | |
| Atopic Dermatitis |
untyped
Associated
|
mechanism: Epidermal Barrier Dysfunction
|
| Contact Dermatitis |
untyped
Risk Factor
|
scoped to subtype: Allergic Contact Dermatitis, Irritant Contact Dermatitis
|
| Inherited Ichthyosis |
untyped
Causative biallelic loss-of-function variants in ichthyosis vulgaris
|
mechanism: Disrupted Keratinocyte Differentiation and Cornification
subtype: Ichthyosis Vulgaris
scoped to subtype: Ichthyosis Vulgaris
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.