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Symbol
Name
ID
Krt16
keratin 16
MGI:96690
Phenotype annotations related to integument
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Palmoplantar blistering
Palmoplantar hyperhidrosis
Palmoplantar keratoderma
Palmar hyperkeratosis
Alopecia
Fingernail dysplasia
Paronychia
Nail dystrophy
Onychogryposis of fingernail
Onychogryposis of toenails
Keratosis pilaris
Cutaneous cyst
Epidermoid cyst
Eruptive vellus hair cyst
Follicular hyperkeratosis
Linear arrays of macular hyperkeratoses in flexural areas
Perioral hyperkeratosis
Congenital bullous ichthyosiform erythroderma
Steatocystoma multiplex
Disease(s) Associated with KRT16
focal nonepidermolytic palmoplantar keratoderma 1
pachyonychia congenita

Mouse Phenotypes
integument phenotype
impaired skin barrier function
hyperkeratosis
skin lesions
thick skin
Availability Mouse Genotype
Krt16tm1(KOMP)Vlcg/Krt16tm1(KOMP)Vlcg *

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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory