Previous symbols: ICR2B. Aliases: DKFZP434G232, LI2.
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 |
|---|---|---|
| Autosomal Recessive Congenital Ichthyosis | causative germline |
mechanism: Biallelic ARCI Gene Defects; Epidermal Lipid Processing and Transport Defect
subtype: ARCI4A
scoped to subtype: ARCI4A
|
| Inherited Ichthyosis |
untyped
Causative biallelic pathogenic variants in autosomal recessive congenital ichthyosis, including harlequin ichthyosis
|
mechanism: Epidermal Lipid Metabolism Defect
subtype: Autosomal Recessive Congenital Ichthyosis
scoped to subtype: Autosomal Recessive Congenital Ichthyosis
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.