- increased bone mineral density / IMPC
- decreased leukocyte cell number / IMPC
- abnormal forelimb morphology / IMPC
- abnormal hindlimb morphology / IMPC
- abnormal autopod morphology / IMPC
- decreased locomotor activity / IMPC
- abnormal gait / IMPC
- decreased exploration in new environment / IMPC
- limb grasping / IMPC
- abnormal digit morphology / IMPC
- decreased vertical activity / IMPC
- abnormal bone structure / IMPC
- decreased lymphocyte cell number / IMPC
C57BL/6NTac-Gdf5em1(IMPC)H/H
Status | Available to order |
EMMA ID | EM:14728 |
Citation information | RRID:IMSR_EM:14728 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 | C57BL/6NTac-Gdf5em1(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Gdf5em1(IMPC)H |
Gene/Transgene symbol | Gdf5 |
Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Acromesomelic dysplasia, Hunter-Thompson type / Orphanet_968
- Brachydactyly type C / Orphanet_93384
- Brachydactyly type A1 / Orphanet_93388
- Angel-shaped phalango-epiphyseal dysplasia / Orphanet_63442
- Fibular aplasia-complex brachydactyly syndrome / Orphanet_2639
- Acromesomelic dysplasia, Grebe type / Orphanet_2098
- Multiple synostoses syndrome / Orphanet_3237
- Proximal symphalangism / Orphanet_3250
- Brachydactyly type A2 / Orphanet_93396
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal autopod morphology / IMPC
- abnormal gait / IMPC
- decreased exploration in new environment / IMPC
- abnormal digit morphology / IMPC
- decreased grip strength / IMPC
- abnormal bone structure / IMPC
- increased bone mineral density / IMPC
- abnormal forelimb morphology / IMPC
- decreased lymphocyte cell number / IMPC
- decreased leukocyte cell number / IMPC
- abnormal hindlimb morphology / IMPC
- decreased locomotor activity / IMPC
- decreased vertical activity / IMPC
- limb grasping / IMPC
MGI phenotypes (gene matching)
- delayed bone ossification / MGI
- abnormal long bone epiphysis morphology / MGI
- abnormal cartilage morphology / MGI
- abnormal cartilage development / MGI
- decreased chondrocyte number / MGI
- short limbs / MGI
- abnormal carpal bone morphology / MGI
- abnormal tibia morphology / MGI
- abnormal femur morphology / MGI
- abnormal autopod morphology / MGI
- decreased body weight / MGI
- reduced male fertility / MGI
- decreased litter size / MGI
- abnormal limb morphology / MGI
- abnormal digit morphology / MGI
- abnormal limb bone morphology / MGI
- abnormal fibula morphology / MGI
- disproportionate dwarf / MGI
- brachyphalangia / MGI
- brachydactyly / MGI
- short tibia / MGI
- short fibula / MGI
- brachypodia / MGI
- abnormal long bone epiphyseal plate morphology / MGI
- abnormal metatarsal bone morphology / MGI
- abnormal metacarpal bone morphology / MGI
- short femur / MGI
- fused joints / MGI
- delayed endochondral bone ossification / MGI
- abnormal long bone morphology / MGI
- short humerus / MGI
- short radius / MGI
- short ulna / MGI
- short metacarpal bones / MGI
- short metatarsal bones / MGI
- decreased length of long bones / MGI
- abnormal tarsal bone morphology / MGI
- abnormal phalanx morphology / MGI
- abnormal patella morphology / MGI
- abnormal limb development / MGI
- abnormal digit development / MGI
- abnormal articular cartilage morphology / MGI
- abnormal endochondral bone ossification / MGI
- fused phalanges / MGI
- micromelia / MGI
- fused carpal bones / MGI
- decreased birth weight / MGI
- abnormal limb long bone morphology / MGI
- joint dislocation / MGI
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