- abnormal frontal bone morphology / MGI
- midline facial cleft / MGI
- abnormal scapula morphology / MGI
- abnormal craniofacial morphology / MGI
- abnormal head morphology / MGI
- increased cranium width / MGI
- abnormal carpal bone morphology / MGI
- abnormal hindlimb morphology / MGI
- abnormal tibia morphology / MGI
- polydactyly / MGI
- abnormal autopod morphology / MGI
- abnormal foot pad morphology / MGI
- clubfoot / MGI
- kinked tail / MGI
- thick tail / MGI
- abnormal diencephalon morphology / MGI
- cranioschisis / MGI
- decreased body weight / MGI
- decreased body size / MGI
- hunched posture / MGI
- decreased embryo size / MGI
- edema / MGI
- hydroencephaly / MGI
- infertility / MGI
- male infertility / MGI
- female infertility / MGI
- abnormal estrous cycle / MGI
- decreased litter size / MGI
- premature death / MGI
- abnormal eye morphology / MGI
- abnormal limb morphology / MGI
- abnormal digit morphology / MGI
- abnormal tail morphology / MGI
- abnormal fibula morphology / MGI
- delayed vaginal opening / MGI
- oligozoospermia / MGI
- short tibia / MGI
- abnormal long bone morphology / MGI
- polysyndactyly / MGI
- scapular bone foramen / MGI
- bowed tibia / MGI
- bowed ulna / MGI
- bowed fibula / MGI
- bowed radius / MGI
- broad limb buds / MGI
- increased lumbar vertebrae number / MGI
- decreased length of long bones / MGI
- decreased testis weight / MGI
- abnormal tarsal bone morphology / MGI
- limbs/digits/tail phenotype / MGI
- craniofacial phenotype / MGI
- abnormal skeleton morphology / MGI
- abnormal thoracic cage shape / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- Wormian bones / MGI
- broad snout / MGI
- wide sagittal suture / MGI
- abnormal anterior fontanelle morphology / MGI
- wide metopic suture / MGI
C3H101H-Dbf/H
Status | Available to order |
EMMA ID | EM:00058 |
Citation information | RRID:IMSR_EM:00058 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | C3H101H-Dbf/H |
Alternative name | Doublefoot, Dbf |
Strain type | Spontaneous |
Allele/Transgene symbol | Dbf |
Gene/Transgene symbol | Dbf |
Information from provider
Provider | Mary Lyon |
Provider affiliation | MRC Mammalian Genetics Unit |
Genetic information | This strain carries a spontaneous mutation which arose in the (C3H/HeH x 101/H)F1 stock. |
Phenotypic information | Mice carrying the Dbf mutation have numerous extra toes on all feet. |
References |
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Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
MGI phenotypes (gene matching)
Literature references
- Doublefoot: a new mouse mutant affecting development of limbs and head.;Lyon M F, Quinney R, Glenister P H, Kerscher S, Guillot P, Boyd Y, ;1996;Genetical research;68;221-31; 9062079
Information on how we integrate external resources can be found here
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