Phenotypes associated with this allele

• Allele Symbol: Sh3gl2^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5513818
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Sh3gl2^tm1b(EUCOMM)Wtsi/Sh3gl2^tm1b(EUCOMM)Wtsi	C57BL/6N-Sh3gl2^tm1b(EUCOMM)Wtsi/Tcp	MGI:5757703

Genotype
MGI:5757703

hm1

• Allelic Composition: Sh3gl2^{tm1b(EUCOMM)Wtsi}/Sh3gl2^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-Sh3gl2^{tm1b(EUCOMM)Wtsi}/Tcp
• Cell Lines: EPD0147_3_E02

Data Sources

IMPC Data for Sh3gl2

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

behavior/neurological

decreased exploration in new environment ( J:211773 )

IMPC - TCP

decreased grip strength ( J:211773 )

♀

IMPC - TCP

homeostasis/metabolism

increased circulating alanine transaminase level ( J:211773 )

♂

IMPC - TCP

increased circulating aspartate transaminase level ( J:211773 )

♂

IMPC - TCP

skeleton

decreased bone mineral content ( J:211773 )

♀

IMPC - TCP

decreased bone mineral density ( J:211773 )

IMPC - TCP