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Symbol
Name
ID

Six1
sine oculis-related homeobox 1
MGI:102780

Phenotype annotations related to renal/urinary system

Darker colors indicate more annotations

Human Phenotypes	Vesicoureteral reflux	Nephroblastoma
Disease(s) Associated with SIX1	Vesicoureteral reflux	Nephroblastoma
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	enlarged kidney	abnormal kidney morphology	abnormal kidney development	absent metanephros	small kidney	renal hypoplasia	absent kidney	short ureter
	Six1^Cwe/Six1^Cwe
	Six1^tm1Kwk/Six1^tm1Kwk
	Six1^tm1Mair/Six1^tm1Mair
	Six1^tm1Rsd/Six1^tm1Rsd
	Six1^em1(IMPC)Mbp/Six1⁺

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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