Phenotypes associated with this allele

• Allele Symbol: Tmem79^{tm1.1(KOMP)Wtsi}
• Allele Name: targeted mutation 1.1, Wellcome Trust Sanger Institute
• Allele ID: MGI:5632528
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Tmem79^tm1.1(KOMP)Wtsi/Tmem79^tm1.1(KOMP)Wtsi	C57BL/6N-Tmem79^tm1.1(KOMP)Wtsi/J	MGI:5797874

Genotype
MGI:5797874

hm1

• Allelic Composition: Tmem79^{tm1.1(KOMP)Wtsi}/Tmem79^{tm1.1(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Tmem79^{tm1.1(KOMP)Wtsi}/J
• Cell Lines: EPD0391_7_D08

Data Sources

IMPC Data for Tmem79

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

behavior/neurological

decreased locomotor activity ( J:211773 )

IMPC - JAX

abnormal sleep behavior ( J:211773 )

IMPC - JAX

cardiovascular system

increased heart weight ( J:211773 )

♂

IMPC - JAX

growth/size/body

increased heart weight ( J:211773 )

♂

IMPC - JAX

hematopoietic system

increased mean corpuscular hemoglobin ( J:211773 )

♂

IMPC - JAX

homeostasis/metabolism

decreased fasting circulating glucose level ( J:211773 )

IMPC - JAX

integument

abnormal coat/ hair morphology ( J:211773 )

IMPC - JAX

abnormal coat appearance ( J:211773 )

IMPC - JAX

vision/eye

abnormal retina morphology ( J:211773 )

♀

IMPC - JAX