Phenotypes associated with this allele

• Allele Symbol: Cstb^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5790639
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cstb^tm1b(EUCOMM)Wtsi/Cstb^tm1b(EUCOMM)Wtsi	C57BL/6N-Cstb^tm1b(EUCOMM)Wtsi/Orl	MGI:6262218

Genotype
MGI:6262218

hm1

• Allelic Composition: Cstb^{tm1b(EUCOMM)Wtsi}/Cstb^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Cstb^{tm1b(EUCOMM)Wtsi}/Orl
• Cell Lines: EPD0533_5_G04

Data Sources

IMPC Data for Cstb

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

behavior/neurological

hyperactivity ( J:211773 )

♂

IMPC - ICS

increased vertical activity ( J:211773 )

♂

IMPC - ICS

growth/size/body

decreased body length ( J:211773 )

♂

IMPC - ICS

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - ICS

hematopoietic system

decreased lymphocyte cell number ( J:211773 )

IMPC - ICS

increased monocyte cell number ( J:211773 )

♂

IMPC - ICS

homeostasis/metabolism

decreased circulating creatinine level ( J:211773 )

IMPC - ICS

increased circulating triglyceride level ( J:211773 )

♂

IMPC - ICS

immune system

decreased lymphocyte cell number ( J:211773 )

IMPC - ICS

increased monocyte cell number ( J:211773 )

♂

IMPC - ICS

limbs/digits/tail

short tibia ( J:211773 )

IMPC - ICS

skeleton

short tibia ( J:211773 )

IMPC - ICS

vision/eye

abnormal eye anterior chamber depth ( J:211773 )

♀

IMPC - ICS

abnormal retina outer nuclear layer morphology ( J:211773 )

IMPC - ICS

decreased total retina thickness ( J:211773 )

♀

IMPC - ICS