Phenotypes associated with this allele

• Allele Symbol: Grm6^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548472
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Grm6^tm1b(EUCOMM)Wtsi/Grm6^tm1b(EUCOMM)Wtsi	C57BL/6N-Grm6^tm1b(EUCOMM)Wtsi/H	MGI:5757203

Genotype
MGI:5757203

hm1

• Allelic Composition: Grm6^{tm1b(EUCOMM)Wtsi}/Grm6^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Grm6^{tm1b(EUCOMM)Wtsi}/H
• Cell Lines: EPD0326_1_G06

Data Sources

IMPC Data for Grm6

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

behavior/neurological

impaired pupillary reflex ( J:211773 )

IMPC - HAR

hyperactivity ( J:211773 )

IMPC - HAR

cardiovascular system

increased heart weight ( J:211773 )

♀

IMPC - HAR

growth/size/body

increased heart weight ( J:211773 )

♀

IMPC - HAR

increased kidney weight ( J:211773 )

IMPC - HAR

renal/urinary system

increased kidney weight ( J:211773 )

IMPC - HAR

vision/eye

impaired pupillary reflex ( J:211773 )

IMPC - HAR

abnormal eye morphology ( J:211773 )

♂

IMPC - HAR

mydriasis ( J:211773 )

IMPC - HAR

cataract ( J:211773 )

♂

IMPC - HAR