Phenotypes associated with this allele

• Allele Symbol: Myb^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5692903
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Myb^tm1b(KOMP)Wtsi/Myb^tm1b(KOMP)Wtsi	C57BL/6N-Myb^tm1b(KOMP)Wtsi/Ucd	MGI:5785081
ht2	Myb^tm1b(KOMP)Wtsi/Myb^+	C57BL/6N-Myb^tm1b(KOMP)Wtsi/Ucd	MGI:5797663

Genotype
MGI:5785081

hm1

• Allelic Composition: Myb^{tm1b(KOMP)Wtsi}/Myb^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Myb^{tm1b(KOMP)Wtsi}/Ucd
• Cell Lines: EPD0322_1_H11

Data Sources

IMPC Data for Myb

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

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

homeostasis/metabolism

edema ( J:211773 )

IMPC - UCD

integument

abnormal skin appearance ( J:211773 )

IMPC - UCD

pallor ( J:211773 )

IMPC - UCD

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

Genotype
MGI:5797663

ht2

• Allelic Composition: Myb^{tm1b(KOMP)Wtsi}/Myb⁺
• Genetic Background: C57BL/6N-Myb^{tm1b(KOMP)Wtsi}/Ucd
• Cell Lines: EPD0322_1_H11

Data Sources

IMPC Data for Myb

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD