Phenotypes associated with this allele

• Allele Symbol: Rcc2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5692719
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Rcc2^tm1b(EUCOMM)Wtsi/Rcc2^tm1b(EUCOMM)Wtsi	C57BL/6N-Rcc2^tm1b(EUCOMM)Wtsi/H	MGI:5757610

Genotype
MGI:5757610

hm1

• Allelic Composition: Rcc2^{tm1b(EUCOMM)Wtsi}/Rcc2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Rcc2^{tm1b(EUCOMM)Wtsi}/H
• Cell Lines: EPD0546_4_B10

Data Sources

IMPC Data for Rcc2

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

cardiovascular system

increased heart weight ( J:211773 )

IMPC - HAR

growth/size/body

increased heart weight ( J:211773 )

IMPC - HAR

hematopoietic system

decreased mean corpuscular volume ( J:211773 )

♂

IMPC - HAR

homeostasis/metabolism

decreased circulating serum albumin level ( J:211773 )

IMPC - HAR

decreased circulating total protein level ( J:211773 )

IMPC - HAR

integument

abnormal coat/hair pigmentation ( J:211773 )

♀

IMPC - HAR

nervous system

abnormal optic disk morphology ( J:211773 )

♂

IMPC - HAR

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

♀

IMPC - HAR

vision/eye

abnormal optic disk morphology ( J:211773 )

♂

IMPC - HAR

abnormal retina morphology ( J:211773 )

IMPC - HAR