Phenotypes associated with this allele

• Allele Symbol: Myo7a^{tm1a(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4431921
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myo7a^tm1a(EUCOMM)Wtsi/Myo7a^tm1a(EUCOMM)Wtsi	C57BL/6N-Myo7a^tm1a(EUCOMM)Wtsi/Wtsi	MGI:5608435

Genotype
MGI:5608435

hm1

• Allelic Composition: Myo7a^{tm1a(EUCOMM)Wtsi}/Myo7a^{tm1a(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Myo7a^{tm1a(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0381_2_B08

Data Sources

IMPC Data for Myo7a

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

behavior/neurological

absent pinna reflex ( J:211773 )

IMPC - WTSI

impaired righting response ( J:211773 )

IMPC - WTSI

trunk curl ( J:211773 )

IMPC - WTSI

stereotypic behavior ( J:211773 )

IMPC - WTSI

homeostasis/metabolism

increased circulating sodium level ( J:211773 )

IMPC - WTSI

increased blood urea nitrogen level ( J:211773 )

♂

IMPC - WTSI

vision/eye

persistence of hyaloid vascular system ( J:211773 )

♀

IMPC - WTSI