Phenotypes associated with this allele

• Allele Symbol: Myo9a^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5636908
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myo9a^tm1b(EUCOMM)Wtsi/Myo9a^tm1b(EUCOMM)Wtsi	C57BL/6N-Myo9a^tm1b(EUCOMM)Wtsi/Wtsi	MGI:5883882

Genotype
MGI:5883882

hm1

• Allelic Composition: Myo9a^{tm1b(EUCOMM)Wtsi}/Myo9a^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Myo9a^{tm1b(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0188_3_A12

Data Sources

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

cardiovascular system

retroesophageal right subclavian artery ( J:239583 )

DMDD

arteriovenous malformation ( J:239583 )

DMDD

embryo

abnormal Mullerian duct morphology ( J:239583 )

DMDD

abnormal Wolffian duct morphology ( J:239583 )

DMDD

homeostasis/metabolism

subcutaneous edema ( J:239583 )

DMDD

immune system

blood in lymph vessels ( J:239583 )

DMDD

integument

subcutaneous edema ( J:239583 )

DMDD

nervous system

small superior cervical ganglion ( J:239583 )

DMDD

reduced sympathetic cervical ganglion size ( J:239583 )

DMDD

renal/urinary system

bifid ureter ( J:239583 )

DMDD

skeleton

fusion of vertebral arches ( J:239583 )

DMDD