Phenotypes associated with this allele

• Allele Symbol: Trim39^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5775770
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Trim39^tm1b(EUCOMM)Hmgu/Trim39^tm1b(EUCOMM)Hmgu	C57BL/6N-Trim39^tm1b(EUCOMM)Hmgu/H	MGI:6263769

Genotype
MGI:6263769

hm1

• Allelic Composition: Trim39^{tm1b(EUCOMM)Hmgu}/Trim39^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Trim39^{tm1b(EUCOMM)Hmgu}/H
• Cell Lines: HEPD0583_9_C02

Data Sources

IMPC Data for Trim39

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

adipose tissue

decreased total body fat amount ( J:211773 )

IMPC - HAR

behavior/neurological

increased grip strength ( J:211773 )

♀

IMPC - HAR

abnormal gait ( J:211773 )

IMPC - HAR

decreased locomotor activity ( J:211773 )

IMPC - HAR

growth/size/body

increased lean body mass ( J:211773 )

IMPC - HAR

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - HAR

hematopoietic system

increased lymphocyte cell number ( J:211773 )

IMPC - HAR

decreased monocyte cell number ( J:211773 )

IMPC - HAR

homeostasis/metabolism

decreased fasting circulating glucose level ( J:211773 )

IMPC - HAR

increased fasting circulating glucose level ( J:211773 )

♂

IMPC - HAR

immune system

increased lymphocyte cell number ( J:211773 )

IMPC - HAR

decreased monocyte cell number ( J:211773 )

IMPC - HAR

integument

abnormal vibrissa morphology ( J:211773 )

IMPC - HAR

absent vibrissae ( J:211773 )

♂

IMPC - HAR

skeleton

increased bone mineral content ( J:211773 )

IMPC - HAR

vision/eye

cornea opacity ( J:211773 )

IMPC - HAR

abnormal retina morphology ( J:211773 )

IMPC - HAR