Phenotypes associated with this allele

• Allele Symbol: Rab3gap2^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5629315
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Rab3gap2^tm1b(KOMP)Wtsi/Rab3gap2^tm1b(KOMP)Wtsi	C57BL/6N-Rab3gap2^tm1b(KOMP)Wtsi/J	MGI:6263301

Genotype
MGI:6263301

hm1

• Allelic Composition: Rab3gap2^{tm1b(KOMP)Wtsi}/Rab3gap2^{tm1b(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Rab3gap2^{tm1b(KOMP)Wtsi}/J
• Cell Lines: EPD0731_3_F01

Data Sources

IMPC Data for Rab3gap2

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

behavior/neurological

hyperactivity ( J:211773 )

IMPC - JAX

cardiovascular system

decreased heart rate ( J:211773 )

♂

IMPC - JAX

prolonged RR interval ( J:211773 )

♂

IMPC - JAX

craniofacial

abnormal snout morphology ( J:211773 )

♀

IMPC - JAX

growth/size/body

abnormal snout morphology ( J:211773 )

♀

IMPC - JAX

hematopoietic system

decreased hematocrit ( J:211773 )

♂

IMPC - JAX

thrombocytopenia ( J:211773 )

♂

IMPC - JAX

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

♂

IMPC - JAX

decreased circulating HDL cholesterol level ( J:211773 )

♂

IMPC - JAX

increased circulating alkaline phosphatase level ( J:211773 )

♂

IMPC - JAX

nervous system

abnormal optic disk morphology ( J:211773 )

♀

IMPC - JAX

vision/eye

abnormal optic disk morphology ( J:211773 )

♀

IMPC - JAX

cataract ( J:211773 )

IMPC - JAX

persistence of hyaloid vascular system ( J:211773 )

IMPC - JAX

narrow eye opening ( J:211773 )

♂

IMPC - JAX