Phenotypes associated with this allele

• Allele Symbol: Myo10^{tm2(KOMP)Wtsi}
• Allele Name: targeted mutation 2, Wellcome Trust Sanger Institute
• Allele ID: MGI:4362966
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myo10^tm2(KOMP)Wtsi/Myo10^tm2(KOMP)Wtsi	C57BL/6N-Myo10^tm2(KOMP)Wtsi/Wtsi	MGI:5608409

Genotype
MGI:5608409

hm1

• Allelic Composition: Myo10^{tm2(KOMP)Wtsi}/Myo10^{tm2(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Myo10^{tm2(KOMP)Wtsi}/Wtsi
• Cell Lines: EPD0272_4_F10

Data Sources

IMPC Data for Myo10

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

behavior/neurological

abnormal response to new environment ( J:211773 )

♀

IMPC - WTSI

impaired pupillary reflex ( J:211773 )

♀

IMPC - WTSI

homeostasis/metabolism

decreased circulating creatinine level ( J:211773 )

♀

IMPC - WTSI

integument

abnormal coat/hair pigmentation ( J:211773 )

IMPC - WTSI

limbs/digits/tail

abnormal digit morphology ( J:211773 )

IMPC - WTSI

fused phalanges ( J:211773 )

IMPC - WTSI

abnormal tail morphology ( J:211773 )

IMPC - WTSI

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

IMPC - WTSI

skeleton

fused phalanges ( J:211773 )

IMPC - WTSI

vision/eye

impaired pupillary reflex ( J:211773 )

♀

IMPC - WTSI

abnormal iris morphology ( J:211773 )

IMPC - WTSI

abnormal cornea morphology ( J:211773 )

♀

IMPC - WTSI

cornea opacity ( J:211773 )

♀

IMPC - WTSI

abnormal lens morphology ( J:211773 )

IMPC - WTSI

fused cornea and lens ( J:211773 )

♀

IMPC - WTSI

cataract ( J:211773 )

IMPC - WTSI

persistence of hyaloid vascular system ( J:211773 )

IMPC - WTSI

abnormal retina morphology ( J:211773 )

♀

IMPC - WTSI