All Phenotypes Fam110b<tm1a(EUCOMM)Wtsi> MGI Mouse

About Help FAQ

Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Fam110b^{tm1a(EUCOMM)Wtsi}
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4433953

Summary

1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Fam110b^{tm1a(EUCOMM)Wtsi}/Fam110b⁺	C57BL/6N-Fam110b^{tm1a(EUCOMM)Wtsi}/Cnrm	MGI:5782079

Allelic Composition	Fam110b^{tm1a(EUCOMM)Wtsi}/Fam110b⁺
Genetic Background	C57BL/6N-Fam110b^{tm1a(EUCOMM)Wtsi}/Cnrm
Cell Lines	EPD0155_3_D10

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fam110b^{tm1a(EUCOMM)Wtsi} mutation (0 available); any Fam110b mutation (126 available)

Data Sources

IMPC Data for Fam110b

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

behavior/neurological

abnormal response to tactile stimuli ( J:165965 )

IMPC - HMGU

hematopoietic system

increased erythrocyte cell number ( J:165965 )

IMPC - HMGU

decreased mature B cell number ( J:165965 )

IMPC - HMGU

increased leukocyte cell number ( J:165965 )

IMPC - HMGU

homeostasis/metabolism

decreased blood urea nitrogen level ( J:165965 )

IMPC - HMGU

immune system

decreased mature B cell number ( J:165965 )

IMPC - HMGU

increased leukocyte cell number ( J:165965 )

IMPC - HMGU

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/12/2024 MGI 6.24