Phenotypes associated with this allele

• Allele Symbol: R3hcc1l^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5617141
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	R3hcc1l^tm1b(KOMP)Wtsi/R3hcc1l^tm1b(KOMP)Wtsi	C57BL/6N-R3hcc1l^tm1b(KOMP)Wtsi/J	MGI:5797754

Genotype
MGI:5797754

hm1

• Allelic Composition: R3hcc1l^{tm1b(KOMP)Wtsi}/R3hcc1l^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-R3hcc1l^{tm1b(KOMP)Wtsi}/J
• Cell Lines: EPD0815_3_G11

Data Sources

IMPC Data for R3hcc1l

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

hematopoietic system

decreased mean corpuscular hemoglobin ( J:211773 )

IMPC - JAX

decreased mean corpuscular volume ( J:211773 )

IMPC - JAX

vision/eye

abnormal iris morphology ( J:211773 )

♀

IMPC - JAX

abnormal placement of pupils ( J:211773 )

♀

IMPC - JAX

irregularly shaped pupil ( J:211773 )

♀

IMPC - JAX

mydriasis ( J:211773 )

♀

IMPC - JAX

persistence of hyaloid vascular system ( J:211773 )

♀

IMPC - JAX