Phenotypes associated with this allele

• Allele Symbol: Myo3b^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5603355
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myo3b^tm1b(EUCOMM)Hmgu/Myo3b^tm1b(EUCOMM)Hmgu	C57BL/6N-Myo3b^tm1b(EUCOMM)Hmgu/J	MGI:5797666

Genotype
MGI:5797666

hm1

• Allelic Composition: Myo3b^{tm1b(EUCOMM)Hmgu}/Myo3b^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Myo3b^{tm1b(EUCOMM)Hmgu}/J
• Cell Lines: HEPD0673_6_D02

Data Sources

IMPC Data for Myo3b

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

behavior/neurological

convulsive seizures ( J:211773 )

♀

IMPC - JAX

cardiovascular system

increased heart weight ( J:211773 )

♂

IMPC - JAX

growth/size/body

increased heart weight ( J:211773 )

♂

IMPC - JAX

hematopoietic system

decreased leukocyte cell number ( J:211773 )

♂

IMPC - JAX

immune system

decreased leukocyte cell number ( J:211773 )

♂

IMPC - JAX

nervous system

convulsive seizures ( J:211773 )

♀

IMPC - JAX

skeleton

abnormal bone structure ( J:211773 )

♀

IMPC - JAX

increased bone mineral content ( J:211773 )

IMPC - JAX