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Symbol
Name
ID
Slc4a1
solute carrier family 4 (anion exchanger), member 1
MGI:109393
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Muscle weakness
Disease(s) Associated with SLC4A1
hereditary spherocytosis

Mouse Phenotypes
decreased ventricle muscle contractility
Availability Mouse Genotype
Slc4a1tm1Llp/Slc4a1tm1Llp

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
04/23/2024
MGI 6.23
The Jackson Laboratory