Phenotypes associated with this allele

• Allele Symbol: Fbxw9^{tm1a(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1a, Wellcome Trust Sanger Institute
• Allele ID: MGI:4441814
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fbxw9^tm1a(EUCOMM)Wtsi/Fbxw9^tm1a(EUCOMM)Wtsi	C57BL/6N-Fbxw9^tm1a(EUCOMM)Wtsi/Bay	MGI:5757108
ht2	Fbxw9^tm1a(EUCOMM)Wtsi/Fbxw9^+	C57BL/6N-Fbxw9^tm1a(EUCOMM)Wtsi/Bay	MGI:5757107

Genotype
MGI:5757108

hm1

• Allelic Composition: Fbxw9^{tm1a(EUCOMM)Wtsi}/Fbxw9^{tm1a(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Fbxw9^{tm1a(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0485_1_H05

Data Sources

IMPC Data for Fbxw9

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

endocrine/exocrine glands

abnormal thyroid gland morphology ( J:211773 )

♂

IMPC - BCM

immune system

absent lymph nodes ( J:211773 )

♂

IMPC - BCM

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

♀

IMPC - BCM

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - BCM

respiratory system

abnormal trachea morphology ( J:211773 )

♂

IMPC - BCM

vision/eye

anophthalmia ( J:211773 )

♂

IMPC - BCM

Genotype
MGI:5757107

ht2

• Allelic Composition: Fbxw9^{tm1a(EUCOMM)Wtsi}/Fbxw9⁺
• Genetic Background: C57BL/6N-Fbxw9^{tm1a(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0485_1_H05

Data Sources

IMPC Data for Fbxw9

hematopoietic system

absent spleen ( J:211773 )

♀

IMPC - BCM

immune system

absent spleen ( J:211773 )

♀

IMPC - BCM