Previous symbols: KPP. Aliases: K10, CK10.
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 |
|---|---|---|
| Epidermolytic Hyperkeratosis 2 | causative germline dominant negativeloss of function |
mechanism: Biallelic KRT10 Null Alleles and Keratin 10 Absence; KRT10 Dominant-Negative Rod-Domain Variant
subtype: AEI1; EHK2A; EHK2B
scoped to subtype: EHK2B
|
| Inherited Ichthyosis |
untyped
Causative heterozygous pathogenic variants in epidermolytic ichthyosis
|
mechanism: Disrupted Keratinocyte Differentiation and Cornification
subtype: Keratinopathic Ichthyosis
scoped to subtype: Keratinopathic Ichthyosis
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.