Phenotypes associated with this allele

• Allele Symbol: Snrnp27^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5548525
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Snrnp27^tm1b(EUCOMM)Wtsi/Snrnp27^tm1b(EUCOMM)Wtsi	C57BL/6N-Snrnp27^tm1b(EUCOMM)Wtsi/Wtsi	MGI:5757752
ht2	Snrnp27^tm1b(EUCOMM)Wtsi/Snrnp27^+	C57BL/6N-Snrnp27^tm1b(EUCOMM)Wtsi/Wtsi	MGI:5757751

Genotype
MGI:5757752

hm1

• Allelic Composition: Snrnp27^{tm1b(EUCOMM)Wtsi}/Snrnp27^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Snrnp27^{tm1b(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0635_3_C07

Data Sources

IMPC Data for Snrnp27

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

mortality/aging

embryonic lethality prior to tooth bud stage ( J:211773 )

IMPC - BCM

embryonic lethality prior to organogenesis ( J:211773 )

IMPC - BCM

preweaning lethality, complete penetrance ( J:211773 )

IMPC - BCM

Genotype
MGI:5757751

ht2

• Allelic Composition: Snrnp27^{tm1b(EUCOMM)Wtsi}/Snrnp27⁺
• Genetic Background: C57BL/6N-Snrnp27^{tm1b(EUCOMM)Wtsi}/Wtsi
• Cell Lines: EPD0635_3_C07

Data Sources

IMPC Data for Snrnp27

behavior/neurological

hyperactivity ( J:211773 )

♀

IMPC - BCM

digestive/alimentary system

abnormal esophagus morphology ( J:211773 )

♂

IMPC - BCM

vision/eye

abnormal retina morphology ( J:211773 )

IMPC - BCM