Symbol Name ID |
Slc4a1
solute carrier family 4 (anion exchanger), member 1 MGI:109393 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Hepatomegaly |
Abdominal distention |
Short stature |
Failure to thrive |
Growth delay |
Disease(s) Associated with SLC4A1 | ||||||
hereditary spherocytosis | ||||||
renal tubular acidosis |
Mouse Phenotypes | cardiac hypertrophy |
decreased body weight |
slow postnatal weight gain |
weight loss |
decreased body size |
postnatal growth retardation |
enlarged spleen |
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Availability | Mouse Genotype | |||||||
Slc4a1tm1Ahc/Slc4a1tm1Ahc | ||||||||
Slc4a1tm1Llp/Slc4a1tm1Llp | ||||||||
Slc4a1tm1Phsl/Slc4a1tm1Phsl |
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 04/16/2024 MGI 6.23 |
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