Symbol Name ID |
Six1
sine oculis-related homeobox 1 MGI:102780 |
Darker colors indicate more annotations |
Human Phenotypes | Vesicoureteral reflux |
Nephroblastoma |
Disease(s) Associated with SIX1 | ||
autosomal dominant nonsyndromic deafness 23 | ||
nephroblastoma |
Mouse Phenotypes | enlarged kidney |
abnormal kidney morphology |
abnormal kidney development |
absent metanephros |
small kidney |
renal hypoplasia |
absent kidney |
short ureter |
|
Availability | Mouse Genotype | ||||||||
Six1Cwe/Six1Cwe | |||||||||
Six1tm1Kwk/Six1tm1Kwk | |||||||||
Six1tm1Mair/Six1tm1Mair | |||||||||
Six1tm1Rsd/Six1tm1Rsd | |||||||||
Six1em1(IMPC)Mbp/Six1+ |
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 08/21/2024 MGI 6.24 |
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