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Symbol
Name
ID
Slc11a1
solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1
MGI:1345275
Phenotype annotations related to integument
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
Availability Mouse Genotype
Slc11a1em1(IMPC)Mbp/Slc11a1em1(IMPC)Mbp

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
03/19/2024
MGI 6.23
The Jackson Laboratory