Phenotypes associated with this allele

• Allele Symbol: Ghrh^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5620318
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ghrh^tm1b(EUCOMM)Wtsi/Ghrh^tm1b(EUCOMM)Wtsi	C57BL/6N-Ghrh^tm1b(EUCOMM)Wtsi/Tcp	MGI:6262520

Genotype
MGI:6262520

hm1

• Allelic Composition: Ghrh^{tm1b(EUCOMM)Wtsi}/Ghrh^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Ghrh^{tm1b(EUCOMM)Wtsi}/Tcp
• Cell Lines: EPD0780_3_A01

Data Sources

IMPC Data for Ghrh

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

adipose tissue

increased total body fat amount ( J:211773 )

IMPC - UCD

behavior/neurological

decreased grip strength ( J:211773 )

♂

IMPC - UCD

cardiovascular system

decreased heart weight ( J:211773 )

IMPC - UCD

growth/size/body

decreased lean body mass ( J:211773 )

IMPC - UCD

decreased body length ( J:211773 )

IMPC - UCD

homeostasis/metabolism

decreased fasting circulating glucose level ( J:211773 )

IMPC - UCD

impaired glucose tolerance ( J:211773 )

IMPC - UCD

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

♀

IMPC - UCD

skeleton

abnormal bone structure ( J:211773 )

♀

IMPC - UCD

decreased bone mineral content ( J:211773 )

IMPC - UCD

decreased bone mineral density ( J:211773 )

IMPC - UCD