All Phenotypes Tardbp<tm1b(EUCOMM)Wtsi> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Tardbp^{tm1b(EUCOMM)Wtsi}
targeted mutation 1b, Wellcome Trust Sanger Institute
MGI:5692816

Summary

2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Tardbp^{tm1b(EUCOMM)Wtsi}/Tardbp^{tm1b(EUCOMM)Wtsi}	C57BL/6N-Tardbp^{tm1b(EUCOMM)Wtsi}/H	MGI:5767821
ht2	Tardbp^{tm1b(EUCOMM)Wtsi}/Tardbp⁺	C57BL/6N-Tardbp^{tm1b(EUCOMM)Wtsi}/H	MGI:5797852

Allelic Composition	Tardbp^{tm1b(EUCOMM)Wtsi}/Tardbp^{tm1b(EUCOMM)Wtsi}
Genetic Background	C57BL/6N-Tardbp^{tm1b(EUCOMM)Wtsi}/H
Cell Lines	EPD0828_4_C03

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tardbp^{tm1b(EUCOMM)Wtsi} mutation (0 available); any Tardbp mutation (68 available)

Data Sources

IMPC Data for Tardbp

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

mortality/aging

embryonic lethality prior to organogenesis ( J:211773 )

IMPC - HAR

preweaning lethality, complete penetrance ( J:211773 )

IMPC - HAR

Allelic Composition	Tardbp^{tm1b(EUCOMM)Wtsi}/Tardbp⁺
Genetic Background	C57BL/6N-Tardbp^{tm1b(EUCOMM)Wtsi}/H
Cell Lines	EPD0828_4_C03

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tardbp^{tm1b(EUCOMM)Wtsi} mutation (0 available); any Tardbp mutation (68 available)

Data Sources

IMPC Data for Tardbp

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

behavior/neurological

abnormal startle reflex ( J:211773 )

IMPC - HAR

hematopoietic system

decreased mean platelet volume ( J:211773 )

IMPC - HAR

homeostasis/metabolism

decreased blood urea nitrogen level ( J:211773 )

IMPC - HAR

skeleton

decreased bone mineral content ( J:211773 )

IMPC - HAR

decreased bone mineral density ( J:211773 )

IMPC - HAR

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)
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