Phenotypes associated with this allele

• Allele Symbol: Ginm1^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5692806
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ginm1^tm1b(EUCOMM)Wtsi/Ginm1^tm1b(EUCOMM)Wtsi	C57BL/6N-Ginm1^tm1b(EUCOMM)Wtsi/BayMmucd	MGI:6370408

Genotype
MGI:6370408

hm1

• Allelic Composition: Ginm1^{tm1b(EUCOMM)Wtsi}/Ginm1^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Ginm1^{tm1b(EUCOMM)Wtsi}/BayMmucd
• Cell Lines: EPD0196_3_H04

Data Sources

IMPC Data for Ginm1

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

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

♀

IMPC - BCM

nervous system

abnormal optic disk morphology ( J:211773 )

♂

IMPC - BCM

vision/eye

abnormal optic disk morphology ( J:211773 )

♂

IMPC - BCM

abnormal retina inner nuclear layer morphology ( J:211773 )

IMPC - BCM

abnormal retina outer nuclear layer morphology ( J:211773 )

♀

IMPC - BCM

decreased total retina thickness ( J:211773 )

IMPC - BCM