Symbol Name ID |
Krt16
keratin 16 MGI:96690 |
* | 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 |
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Availability | Mouse Genotype | |||||
Krt16tm1(KOMP)Vlcg/Krt16tm1(KOMP)Vlcg | * |
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 |
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