Phenotypes associated with this allele

• Allele Symbol: Fam53b^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5548690
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Fam53b^tm1b(EUCOMM)Hmgu/Fam53b^tm1b(EUCOMM)Hmgu	C57BL/6N-Fam53b^tm1b(EUCOMM)Hmgu/Cnrm	MGI:5757087

Genotype
MGI:5757087

hm1

• Allelic Composition: Fam53b^{tm1b(EUCOMM)Hmgu}/Fam53b^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Fam53b^{tm1b(EUCOMM)Hmgu}/Cnrm
• Cell Lines: HEPD0667_7_D08

Data Sources

IMPC Data for Fam53b

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

cardiovascular system

increased cardiac stroke volume ( J:211773 )

♀

IMPC - HMGU

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - HMGU

hematopoietic system

decreased erythrocyte cell number ( J:211773 )

IMPC - HMGU

increased mean corpuscular hemoglobin ( J:211773 )

IMPC - HMGU

increased mean corpuscular volume ( J:211773 )

IMPC - HMGU

decreased red blood cell distribution width ( J:211773 )

IMPC - HMGU

homeostasis/metabolism

increased circulating fructosamine level ( J:211773 )

IMPC - HMGU

increased circulating sodium level ( J:211773 )

♀

IMPC - HMGU

nervous system

decreased prepulse inhibition ( J:211773 )

♀

IMPC - HMGU