Phenotypes associated with this allele

• Allele Symbol: Slc7a11^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548466
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Slc7a11^tm1b(EUCOMM)Wtsi/Slc7a11^tm1b(EUCOMM)Wtsi	C57BL/6N-Slc7a11^tm1b(EUCOMM)Wtsi/Ics	MGI:5757733

Genotype
MGI:5757733

hm1

• Allelic Composition: Slc7a11^{tm1b(EUCOMM)Wtsi}/Slc7a11^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Slc7a11^{tm1b(EUCOMM)Wtsi}/Ics
• Cell Lines: EPD0508_3_E02

Data Sources

IMPC Data for Slc7a11

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

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - ICS

homeostasis/metabolism

increased circulating glucose level ( J:211773 )

♂

IMPC - ICS

nervous system

abnormal optic disk morphology ( J:211773 )

♀

IMPC - ICS

vision/eye

abnormal optic disk morphology ( J:211773 )

♀

IMPC - ICS

abnormal vitreous body morphology ( J:211773 )

IMPC - ICS