Phenotypes associated with this allele

• Allele Symbol: Cnih2^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5635040
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cnih2^tm1b(KOMP)Wtsi/Cnih2^tm1b(KOMP)Wtsi	B6N(Cg)-Cnih2^tm1b(KOMP)Wtsi/J	MGI:6262172

Genotype
MGI:6262172

hm1

• Allelic Composition: Cnih2^{tm1b(KOMP)Wtsi}/Cnih2^{tm1b(KOMP)Wtsi}
• Genetic Background: B6N(Cg)-Cnih2^{tm1b(KOMP)Wtsi}/J
• Cell Lines: EPD0742_2_D11

Data Sources

IMPC Data for Cnih2

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

behavior/neurological

increased exploration in new environment ( J:211773 )

IMPC - JAX

abnormal locomotor behavior ( J:211773 )

IMPC - JAX

hyperactivity ( J:211773 )

IMPC - JAX

increased vertical activity ( J:211773 )

♀

IMPC - JAX

homeostasis/metabolism

decreased circulating calcium level ( J:211773 )

IMPC - JAX

increased circulating alkaline phosphatase level ( J:211773 )

IMPC - JAX

skeleton

abnormal bone structure ( J:211773 )

♀

IMPC - JAX