Phenotypes associated with this allele

• Allele Symbol: Oplah^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548658
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Oplah^tm1b(KOMP)Wtsi/Oplah^tm1b(KOMP)Wtsi	C57BL/6N-Oplah^tm1b(KOMP)Wtsi/Ieg	MGI:5757459

Genotype
MGI:5757459

hm1

• Allelic Composition: Oplah^{tm1b(KOMP)Wtsi}/Oplah^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Oplah^{tm1b(KOMP)Wtsi}/Ieg
• Cell Lines: EPD0244_4_F09

Data Sources

IMPC Data for Oplah

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

behavior/neurological

increased startle reflex ( J:211773 )

♂

IMPC - HMGU

cardiovascular system

decreased heart rate ( J:211773 )

♀

IMPC - HMGU

hematopoietic system

decreased red blood cell distribution width ( J:211773 )

♀

IMPC - HMGU

homeostasis/metabolism

decreased circulating unsaturated transferrin level ( J:211773 )

♀

IMPC - HMGU

vision/eye

abnormal lens morphology ( J:211773 )

♂

IMPC - HMGU

cataract ( J:211773 )

♂

IMPC - HMGU