About Help FAQ

Symbol
Name
ID

Krt2
keratin 2
MGI:96699

Phenotype annotations related to integument

Darker colors indicate more annotations

Human Phenotypes	Palmoplantar keratoderma	Erythema	Abnormal blistering of the skin	Acantholysis	Thin skin	Ichthyosis	Congenital bullous ichthyosiform erythroderma
Disease(s) Associated with KRT2
bullous congenital ichthyosiform erythroderma

Mouse Phenotypes

abnormal keratinocyte differentiation

increased keratinocyte proliferation

increased ear pigmentation

impaired skin barrier function

skin inflammation

abnormal corneocyte morphology

hyperkeratosis

orthokeratosis

thick epidermis stratum granulosum

hypergranulosis

acanthosis

abnormal epidermis suprabasal layer morphology

epidermal hyperplasia

thick epidermis

scaly skin

abnormal skin pigmentation

increased foot pad pigmentation

increased tail pigmentation

Availability

Mouse Genotype

Krt2^Mhdadsk2/Krt2^Mhdadsk2

Krt2^{tm1a(KOMP)Wtsi}/Krt2^{tm1a(KOMP)Wtsi}

Krt2^Mhdadsk2/Krt2⁺

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/28/2024 MGI 6.13