Phenotypes associated with this allele

• Allele Symbol: Ccnt2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5637066
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ccnt2^tm1b(EUCOMM)Wtsi/Ccnt2^tm1b(EUCOMM)Wtsi	C57BL/6N-Ccnt2^tm1b(EUCOMM)Wtsi/Bay	MGI:5812997
ht2	Ccnt2^tm1b(EUCOMM)Wtsi/Ccnt2^+	C57BL/6N-Ccnt2^tm1b(EUCOMM)Wtsi/Bay	MGI:6262060

Genotype
MGI:5812997

hm1

• Allelic Composition: Ccnt2^{tm1b(EUCOMM)Wtsi}/Ccnt2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Ccnt2^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0116_1_G01

Data Sources

IMPC Data for Ccnt2

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

behavior/neurological

unresponsive to tactile stimuli ( J:211773 )

IMPC - BCM

cardiovascular system

abnormal retina blood vessel morphology ( J:211773 )

IMPC - BCM

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

IMPC - BCM

reproductive system

female infertility ( J:211773 )

♀

IMPC - BCM

male infertility ( J:211773 )

♂

IMPC - BCM

vision/eye

abnormal retina blood vessel morphology ( J:211773 )

IMPC - BCM

Genotype
MGI:6262060

ht2

• Allelic Composition: Ccnt2^{tm1b(EUCOMM)Wtsi}/Ccnt2⁺
• Genetic Background: C57BL/6N-Ccnt2^{tm1b(EUCOMM)Wtsi}/Bay
• Cell Lines: EPD0116_1_G01

Data Sources

IMPC Data for Ccnt2

behavior/neurological

unresponsive to tactile stimuli ( J:211773 )

IMPC - BCM

integument

abnormal skin coloration ( J:211773 )

IMPC - BCM

vision/eye

abnormal retina outer nuclear layer morphology ( J:211773 )

IMPC - BCM

decreased total retina thickness ( J:211773 )

IMPC - BCM