Phenotypes associated with this allele

• Allele Symbol: Ropn1l^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548780
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ropn1l^tm1b(EUCOMM)Wtsi/Ropn1l^tm1b(EUCOMM)Wtsi	C57BL/6N-Ropn1l^tm1b(EUCOMM)Wtsi/Wtsi	MGI:5757651

Genotype
MGI:5757651

hm1

• Allelic Composition: Ropn1l^{tm1b(EUCOMM)Wtsi}/Ropn1l^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Ropn1l^{tm1b(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0654_2_A03

Data Sources

IMPC Data for Ropn1l

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

behavior/neurological

decreased grip strength ( J:211773 )

♂

IMPC - WTSI

craniofacial

abnormal tooth morphology ( J:211773 )

IMPC - WTSI

abnormal snout morphology ( J:211773 )

IMPC - WTSI

growth/size/body

abnormal tooth morphology ( J:211773 )

IMPC - WTSI

abnormal snout morphology ( J:211773 )

IMPC - WTSI

skeleton

abnormal tooth morphology ( J:211773 )

IMPC - WTSI

abnormal spine curvature ( J:211773 )

♂

IMPC - WTSI

kyphosis ( J:211773 )

♂

IMPC - WTSI