Phenotypes associated with this allele

• Allele Symbol: Mkrn2^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548531
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Mkrn2^tm1b(KOMP)Wtsi/Mkrn2^tm1b(KOMP)Wtsi	C57BL/6N-Mkrn2^tm1b(KOMP)Wtsi/Wtsi	MGI:5797656

Genotype
MGI:5797656

hm1

• Allelic Composition: Mkrn2^{tm1b(KOMP)Wtsi}/Mkrn2^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Mkrn2^{tm1b(KOMP)Wtsi}/Wtsi
• Cell Lines: EPD0748_1_C12

Data Sources

IMPC Data for Mkrn2

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

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - WTSI

hematopoietic system

decreased dendritic epidermal T cell number ( J:211773 )

IMPC - WTSI

homeostasis/metabolism

increased circulating aspartate transaminase level ( J:211773 )

♀

IMPC - WTSI

immune system

decreased dendritic epidermal T cell number ( J:211773 )

IMPC - WTSI

integument

decreased dendritic epidermal T cell number ( J:211773 )

IMPC - WTSI

reproductive system

male infertility ( J:211773 )

♂

IMPC - WTSI