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Symbol
Name
ID
Slc45a2
solute carrier family 45, member 2
MGI:2153040
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Blue irides
Macular hypoplasia
Hypopigmentation of the fundus
Nystagmus
Visual impairment
Disease(s) Associated with SLC45A2
oculocutaneous albinism type IV

Mouse Phenotypes
abnormal eye pigmentation
absent eye pigmentation
decreased eye pigmentation
Availability Mouse Genotype
Slc45a2Ltct/Slc45a2Ltct
Slc45a2uw-2Btlr/Slc45a2uw-2Btlr
Slc45a2uw-3Btlr/Slc45a2uw-3Btlr
Slc45a2uw-4Btlr/Slc45a2uw-4Btlr
Slc45a2uw-4J/Slc45a2uw-4J
Slc45a2uw-5J/Slc45a2uw-5J
Slc45a2uw-6Btlr/Slc45a2uw-6Btlr
Slc45a2uw-6J/Slc45a2uw-6J
Slc45a2uw-7Btlr/Slc45a2uw-7Btlr
Slc45a2uw-7J/Slc45a2uw-7J
Slc45a2uw-Btlr/Slc45a2uw-Btlr
Slc45a2uw-d/Slc45a2uw-d
Slc45a2uw/Slc45a2uw

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
05/21/2024
MGI 6.23
The Jackson Laboratory