Ichthyosis Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores 2025
Category disease or phenotype associations
Type disease
Description An abnormality of the skin characterized the presence of excessive amounts of dry surface scales on the skin resulting from an abnormality of keratinization. (Human Phenotype Ontology, HP_0008064)
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Genes

12 genes involed in the disease Ichthyosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Symbol Name Standardized Value
ALOX12B arachidonate 12-lipoxygenase, 12R type 5.0
CASP14 caspase 14, apoptosis-related cysteine peptidase 5.0
LIPN lipase, family member N 5.0
TGM1 transglutaminase 1 5.0
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12 5.0
KRT10 keratin 10, type I 5.0
KRT1 keratin 1, type II 5.0
CERS3 ceramide synthase 3 5.0
NIPAL4 NIPA-like domain containing 4 5.0
CYP4F22 cytochrome P450, family 4, subfamily F, polypeptide 22 5.0
ALOXE3 arachidonate lipoxygenase 3 5.0
PNPLA1 patatin-like phospholipase domain containing 1 5.0