- delayed bone ossification / MGI
- rectal prolapse / MGI
- abnormal forelimb morphology / MGI
- abnormal carpal bone morphology / MGI
- absent carpal bone / MGI
- polydactyly / MGI
- syndactyly / MGI
- interdigital webbing / MGI
- abnormal autopod morphology / MGI
- abnormal smooth muscle morphology / MGI
- decreased body weight / MGI
- reduced male fertility / MGI
- male infertility / MGI
- abnormal seminal vesicle morphology / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal digit morphology / MGI
- brachyphalangia / MGI
- brachydactyly / MGI
- abnormal metatarsal bone morphology / MGI
- abnormal metacarpal bone morphology / MGI
- delayed endochondral bone ossification / MGI
- polysyndactyly / MGI
- short radius / MGI
- short ulna / MGI
- bowed ulna / MGI
- bowed radius / MGI
- sacral vertebral fusion / MGI
- short metacarpal bones / MGI
- short metatarsal bones / MGI
- decreased metacarpal bone number / MGI
- decreased metatarsal bone number / MGI
- abnormal anus morphology / MGI
- abnormal tarsal bone morphology / MGI
- ectrodactyly / MGI
- abnormal phalanx morphology / MGI
- limbs/digits/tail phenotype / MGI
- endocrine/exocrine gland phenotype / MGI
- abnormal limb development / MGI
- abnormal digit development / MGI
- absent male preputial gland / MGI
- abnormal bone ossification / MGI
- abnormal hallux morphology / MGI
- abnormal internal anal sphincter morphology / MGI
- postaxial polydactyly / MGI
- absent female preputial gland / MGI
B6.129S2-Evx2/Hoxd13tm4(cre)Ddu Del(2Hoxd11-Hoxd13)27Ddu/Orl
Status | Available to order |
EMMA ID | EM:01220 |
Citation information | RRID:IMSR_EM:01220 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 | B6.129S2-Evx2/Hoxd13tm4(cre)Ddu Del(2Hoxd11-Hoxd13)27Ddu/Orl |
Alternative name | P1Del |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Evx2/Hoxd13tm4(cre)Ddu, Del(2Hoxd11-Hoxd13)27Ddu |
Gene/Transgene symbol | Hoxd13, Del(2Hoxd11-Hoxd13)27Ddu |
Information from provider
Provider | Duboule Denis |
Provider affiliation | Laboratoire Moléculaire et Morphogenèse |
Genetic information | Insertion of the Hoxd11Cre transgene between Evx2 and Hoxd13 and deletion of Hoxd13 to Hoxd11 genes by TArgeted MEiotic REcombination (TAMERE). |
Phenotypic information | None. |
Breeding history | Backcross: N=10; Intercross: N=10. |
References |
|
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Brachydactyly-syndactyly, Zhao type / Orphanet_93409
- Brachydactyly type E / Orphanet_93387
- Synpolydactyly type 1 / Orphanet_295195
- Zygodactyly type 3 / Orphanet_295191
- Syndactyly type 5 / Orphanet_93406
MGI phenotypes (gene matching)
Literature references
- A nested deletion approach to generate Cre deleter mice with progressive Hox profiles.;Hérault Yann, Kmita Marie, Sawaya Chadi C, Duboule Denis, ;2002;The International journal of developmental biology;46;185-91; 11902682
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