Phenotypes associated with this allele

• Allele Symbol: Tmem51^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5792558
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Tmem51^tm1b(EUCOMM)Hmgu/Tmem51^tm1b(EUCOMM)Hmgu	C57BL/6N-Tmem51^tm1b(EUCOMM)Hmgu/H	MGI:6263722

Genotype
MGI:6263722

hm1

• Allelic Composition: Tmem51^{tm1b(EUCOMM)Hmgu}/Tmem51^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Tmem51^{tm1b(EUCOMM)Hmgu}/H
• Cell Lines: HEPD0725_6_C05

Data Sources

IMPC Data for Tmem51

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

behavior/neurological

abnormal startle reflex ( J:211773 )

IMPC - HAR

decreased startle reflex ( J:211773 )

IMPC - HAR

abnormal gait ( J:211773 )

IMPC - HAR

hearing/vestibular/ear

abnormal auditory brainstem response ( J:211773 )

IMPC - HAR

homeostasis/metabolism

decreased circulating fructosamine level ( J:211773 )

♀

IMPC - HAR

increased circulating HDL cholesterol level ( J:211773 )

♂

IMPC - HAR

nervous system

decreased prepulse inhibition ( J:211773 )

IMPC - HAR

vision/eye

abnormal retina morphology ( J:211773 )

♂

IMPC - HAR