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Symbol Name ID |
Fermt1
fermitin family member 1 MGI:2443583 |
| Darker colors indicate more annotations |
| Human Phenotypes | Palmoplantar hyperkeratosis |
Telangiectasia of the skin |
Ridged nail |
Acral blistering |
Spotty hyperpigmentation |
Spotty hypopigmentation |
Cutaneous photosensitivity |
Fragile skin |
Dermal atrophy |
Diffuse skin atrophy |
Poikiloderma |
| Disease(s) Associated with FERMT1 | |||||||||||
| Kindler syndrome |
| Mouse Phenotypes | decreased keratinocyte adhesion |
decreased keratinocyte proliferation |
thin epidermis |
skin atrophy |
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| Availability | Mouse Genotype | ||||
| Fermt1tm1Ref/Fermt1tm1Ref | |||||
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 04/16/2024 MGI 6.23 |
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