- 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 |
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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