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

Mouse Phenotypes
abnormal blood homeostasis
increased blood osmolality
acidemia
increased blood urea nitrogen level
decreased circulating bicarbonate level
increased circulating phosphate level
dehydration
increased circulating chloride level
metabolic acidosis
abnormal urine homeostasis
increased urine calcium level
decreased urine osmolality
increased urine pH
abnormal physiological response to xenobiotic
increased sensitivity to xenobiotic induced morbidity/mortality
Availability Mouse Genotype
Slc4a1tm1Llp/Slc4a1tm1Llp
Slc4a1tm1Llp/Slc4a1+

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
01/07/2020
MGI 6.14
The Jackson Laboratory