Symbol Name ID |
Spta1
spectrin alpha, erythrocytic 1 MGI:98385 |
Darker colors indicate more annotations |
Human Phenotypes | Hepatomegaly |
Cholelithiasis |
Jaundice |
Disease(s) Associated with SPTA1 | |||
hereditary spherocytosis |
Mouse Phenotypes | dilated liver sinusoidal space |
liver vascular congestion |
focal hepatic necrosis |
enlarged liver |
increased liver iron level |
gallstones |
abnormal liver morphology |
liver degeneration |
jaundice |
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Availability | Mouse Genotype | |||||||||
Spta1ihj/Spta1ihj | ||||||||||
Spta1sph-2Bc/Spta1sph-2Bc | ||||||||||
Spta1sph-3J/Spta1sph-3J | ||||||||||
Spta1sph-4J/Spta1sph-4J | ||||||||||
Spta1sph-Dem/Spta1sph-Dem | ||||||||||
Spta1sph-ha/Spta1sph-ha | ||||||||||
Spta1sph/Spta1sph |
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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