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Allele : Eya1<bor> EYA transcriptional coactivator and phosphatase 1; branchio otorenal syndrome

Primary Identifier	MGI:1857803	Allele Type	Spontaneous
Gene	Eya1	Inheritance Mode	Recessive
Strain of Origin	C3HeB/FeJ	Is Recombinase	false
Is Wild Type	false

molecularNote

Insertion of an intracisternal A particle (IAP) element in intron 7. The presence of the IAP insertion was associated with reduced expression of the normal mRNA and aberrant splicing.

mutations:
Transposon insertion

earliestPublication:
Johnson KR, et al. (1999) Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome. Hum Mol Genet 8(4):645-53

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

Other

4 Carried By

0 Driven By

10 Publication categories

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