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Btbd9tm1d(EUCOMM)Wtsi
Targeted Allele Detail
Nomenclature
Symbol: Btbd9tm1d(EUCOMM)Wtsi
Name: BTB (POZ) domain containing 9; targeted mutation 1d, Wellcome Trust Sanger Institute
MGI ID: MGI:6488232
Gene: Btbd9  Location: Chr17:30434498-30795462 bp, - strand  Genetic Position: Chr17, 15.62 cM, cytoband B1
Mutation
origin
Mutant Cell Line:  EPD0631_3_A09
Germline Transmission:  Earliest citation of germline transmission: J:282582
Parent Cell Line:  JM8A3.N1 (ES Cell)
Strain of Origin:  C57BL/6N-Atm1Brd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion     Vector: L1L2_Bact_P
 
Mutation detailsCre-mediated excision of the floxed B9d1tm1c(EUCOMM)Wtsi allele removed exon 4. (J:282582)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Btbd9 Mutation:  40 strains or lines available
References
Original:  J:282582 Lyu S, et al., The role of BTBD9 in the cerebral cortex and the pathogenesis of restless legs syndrome. Exp Neurol. 2020 Jan;323:113111
All:  4 reference(s)

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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last database update
01/18/2022
MGI 6.17
The Jackson Laboratory