Phenotypes associated with this allele

• Allele Symbol: Epb41l1^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5661983
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Epb41l1^tm1b(EUCOMM)Wtsi/Epb41l1^tm1b(EUCOMM)Wtsi	C57BL/6N-Epb41l1^tm1b(EUCOMM)Wtsi/J	MGI:6262378

Genotype
MGI:6262378

hm1

• Allelic Composition: Epb41l1^{tm1b(EUCOMM)Wtsi}/Epb41l1^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Epb41l1^{tm1b(EUCOMM)Wtsi}/J
• Cell Lines: EPD0628_1_C10

Data Sources

IMPC Data for Epb41l1

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

adipose tissue

decreased total body fat amount ( J:211773 )

♂

IMPC - JAX

behavior/neurological

increased exploration in new environment ( J:211773 )

IMPC - JAX

decreased thigmotaxis ( J:211773 )

♀

IMPC - JAX

increased startle reflex ( J:211773 )

♂

IMPC - JAX

decreased grip strength ( J:211773 )

♂

IMPC - JAX

abnormal locomotor behavior ( J:211773 )

♀

IMPC - JAX

hyperactivity ( J:211773 )

IMPC - JAX

growth/size/body

increased lean body mass ( J:211773 )

♂

IMPC - JAX

homeostasis/metabolism

increased fasting circulating glucose level ( J:211773 )

♀

IMPC - JAX

increased circulating aspartate transaminase level ( J:211773 )

♂

IMPC - JAX

improved glucose tolerance ( J:211773 )

♂

IMPC - JAX

pigmentation

abnormal iris pigmentation ( J:211773 )

♂

IMPC - JAX

skeleton

increased bone mineral content ( J:211773 )

♂

IMPC - JAX

vision/eye

abnormal iris pigmentation ( J:211773 )

♂

IMPC - JAX

sclerocornea ( J:211773 )

♂

IMPC - JAX

abnormal eyelid morphology ( J:211773 )

♂

IMPC - JAX