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Symbol Name ID |
Whrn whirlin MGI:2682003 |
Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases
Whrntm1a(EUCOMM)Wtsi
whirlin; targeted mutation 1a, Wellcome Trust Sanger Institute 4 Targeted (Floxed/Frt) behavior, hearing/vestibular/ear, integument
Whrntm1Tili
whirlin; targeted mutation 1, Tiansen Li 4 Targeted (knock-out) hearing/vestibular/ear, nervous system, vision/eye Usher Syndrome, Type Iid; USH2D 611383
Whrnwi
whirlin; whirler 4 wi Spontaneous adipose, behavior, cardiovascular, endocrine/exocrine, growth/size, hearing/vestibular/ear, hematopoietic, homeostasis, immune, liver/biliary, nervous system, pigmentation, renal/urinary, reproductive, vision/eye Deafness, Autosomal Recessive 31; DFNB31 607084
Whrntm1e(EUCOMM)Wtsi
whirlin; targeted mutation 1e, Wellcome Trust Sanger Institute 4 Targeted (Reporter)
(Cell Line)
Whrntm2a(EUCOMM)Wtsi
whirlin; targeted mutation 2a, Wellcome Trust Sanger Institute 4 Targeted (Floxed/Frt)
(Cell Line)
Whrntm2e(EUCOMM)Wtsi
whirlin; targeted mutation 2e, Wellcome Trust Sanger Institute 4 Targeted (Reporter)
(Cell Line)
Whrntm3a(EUCOMM)Wtsi
whirlin; targeted mutation 3a, Wellcome Trust Sanger Institute 4 Targeted (Floxed/Frt)
(Cell Line)
Whrntm3e(EUCOMM)Wtsi
whirlin; targeted mutation 3e, Wellcome Trust Sanger Institute 4 Targeted (Reporter)
(Cell Line)
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/12/2013 MGI 5.14 |
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