Symbol Name ID |
Slc11a1
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 MGI:1345275 |
Darker colors indicate more annotations |
Human Phenotypes | Absent eyebrow |
Loss of eyelashes |
Gynecomastia |
Erythema |
Telangiectasia |
Erythema nodosum |
Discoid lupus rash |
Maculopapular exanthema |
Malar rash |
Patchy alopecia |
Alopecia |
Sparse body hair |
Hypohidrosis |
Abnormality of the skin |
Abnormal skin morphology |
Hyperpigmentation of the skin |
Hypopigmentation of the skin |
Cutaneous photosensitivity |
Hypopigmented macule |
Verrucous papule |
Skin nodule |
Subcutaneous nodule |
Skin plaque |
Urticarial plaque |
Acral ulceration |
Penetrating foot ulcers |
Hyperkeratosis |
Sclerodactyly |
Scleroderma |
Disease(s) Associated with SLC11A1 | |||||||||||||||||||||||||||||
Behcet's disease | |||||||||||||||||||||||||||||
leprosy | |||||||||||||||||||||||||||||
sarcoidosis | |||||||||||||||||||||||||||||
systemic lupus erythematosus | |||||||||||||||||||||||||||||
systemic scleroderma |
Mouse Phenotypes | abnormal skin morphology |
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Availability | Mouse Genotype | |
Slc11a1em1(IMPC)Mbp/Slc11a1em1(IMPC)Mbp |
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 03/19/2024 MGI 6.23 |
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