- 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/Orl
Status | Available to order |
EMMA ID | EM:01216 |
International strain name | B6.129S2-Evx2/Hoxd13tm4(cre)Ddu/Orl |
Alternative name | B6.129S2 TgN13(d11Cre) |
Strain type | Targeted Mutant Strains : Knock-in |
Allele/Transgene symbol | Evx2/Hoxd13tm4(cre)Ddu |
Gene/Transgene symbol | Hoxd13 |
Information from provider
Provider | Duboule Denis |
Provider affiliation | Laboratoire Moléculaire et Morphogenèse |
Genetic information | Insertion, by homologous recombination, of the Hoxd11Cre transgene between Evx2 and Hoxd13. In this transgene the sequence of cre recombinase with a polyadenylation signal is introduced within the first exon of inserted Hoxd11 gene; the partial gene replacement leads to the synthesis of the cre recombinase without any residues from Hoxd11. |
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
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).