Phenotypes associated with this allele

• Allele Symbol: Ucp1^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5692920
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ucp1^tm1b(EUCOMM)Hmgu/Ucp1^tm1b(EUCOMM)Hmgu	C57BL/6N-Ucp1^tm1b(EUCOMM)Hmgu/Ieg	MGI:5757852

Genotype
MGI:5757852

hm1

• Allelic Composition: Ucp1^{tm1b(EUCOMM)Hmgu}/Ucp1^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Ucp1^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0676_4_E07

Data Sources

IMPC Data for Ucp1

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

cardiovascular system

thick ventricular wall ( J:211773 )

♀

IMPC - HMGU

abnormal sinus arrhythmia ( J:211773 )

IMPC - HMGU

abnormal QT variability ( J:211773 )

♀

IMPC - HMGU

hematopoietic system

increased erythrocyte cell number ( J:211773 )

♂

IMPC - HMGU

increased hematocrit ( J:211773 )

♂

IMPC - HMGU

homeostasis/metabolism

decreased circulating triglyceride level ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

♂

IMPC - HMGU

cataract ( J:211773 )

IMPC - HMGU