Phenotypes Associated with This Genotype

Genotype
MGI:6461168

ht2

• Allelic Composition: Cog7^{tm1b(EUCOMM)Hmgu}/Cog7⁺
• Genetic Background: B6N(Cg)-Cog7^{tm1b(EUCOMM)Hmgu}/J
• Cell Lines: HEPD0681_4_B12

Data Sources

IMPC Data for Cog7

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

behavior/neurological

impaired pupillary reflex ( J:211773 )

♀

IMPC - JAX

cardiovascular system

abnormal sinus arrhythmia ( J:211773 )

♀

IMPC - JAX

vision/eye

impaired pupillary reflex ( J:211773 )

♀

IMPC - JAX

cornea deposits ( J:211773 )

♀

IMPC - JAX