C57BL/6NTac-Bmp7tm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:04863 |
International strain name | C57BL/6NTac-Bmp7tm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0510_3_C07 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Bmp7tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Bmp7 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0510_3_C07. For further details on the construction of this clone see the 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 |
Animals used for archiving | heterozygous C57BL/6NTac |
Breeding at archiving centre | Chimeras were mated to C57BL/6NTac USA and maintained on this background thereafter. |
Disease and phenotype information
IMPC phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal cochlea morphology / MGI
- delayed bone ossification / MGI
- decreased bone mineral density / MGI
- abnormal basioccipital bone morphology / MGI
- abnormal basisphenoid bone morphology / MGI
- cleft palate / MGI
- growth retardation of molars / MGI
- abnormal vertebrae morphology / MGI
- rib bifurcation / MGI
- rib fusion / MGI
- abnormal sternum morphology / MGI
- abnormal xiphoid process morphology / MGI
- abnormal hair follicle morphology / MGI
- abnormal craniofacial morphology / MGI
- abnormal cranium morphology / MGI
- abnormal maxilla morphology / MGI
- abnormal mandible morphology / MGI
- abnormal kidney development / MGI
- hydroureter / MGI
- polydactyly / MGI
- kinked tail / MGI
- tremors / MGI
- exencephaly / MGI
- decreased body weight / MGI
- decreased body size / MGI
- abnormal eye development / MGI
- abnormal lens vesicle development / MGI
- anophthalmia / MGI
- microphthalmia / MGI
- impaired coordination / MGI
- abnormal apical ectodermal ridge morphology / MGI
- premature death / MGI
- abnormal vibrissa morphology / MGI
- abnormal tooth morphology / MGI
- abnormal digit morphology / MGI
- abnormal axial skeleton morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal cricoid cartilage morphology / MGI
- abnormal thyroid cartilage morphology / MGI
- abnormal semicircular canal morphology / MGI
- abnormal molar morphology / MGI
- small kidney / MGI
- abnormal sacral vertebrae morphology / MGI
- abnormal hyoid bone morphology / MGI
- aphakia / MGI
- abnormal soft palate morphology / MGI
- abnormal alisphenoid bone morphology / MGI
- decreased rib number / MGI
- renal hypoplasia / MGI
- dilated renal glomerular capsule / MGI
- kidney cysts / MGI
- abnormal hard palate morphology / MGI
- abnormal craniofacial development / MGI
- decreased fetal size / MGI
- small pterygoid bone / MGI
- small basisphenoid bone / MGI
- basisphenoid bone foramen / MGI
- decreased renal glomerulus number / MGI
- abnormal maxillary shelf morphology / MGI
- broad limb buds / MGI
- fusion of vertebral bodies / MGI
- decreased lumbar vertebrae number / MGI
- xiphoid process foramen / MGI
- abnormal nasal capsule morphology / MGI
- abnormal distal convoluted tubule morphology / MGI
- absent upper incisors / MGI
- abnormal retinal pigmentation / MGI
- abnormal middle ear ossicle morphology / MGI
- eyelids fail to open / MGI
- abnormal retinal pigment epithelium morphology / MGI
- abnormal renal glomerulus morphology / MGI
- cardiovascular system phenotype / MGI
- skeleton phenotype / MGI
- abnormal skeleton morphology / MGI
- retinal pigment epithelium atrophy / MGI
- decreased molar number / MGI
- asymmetric sternocostal joints / MGI
- abnormal sternocostal joint morphology / MGI
- polycystic kidney / MGI
- abnormal vibrissa number / MGI
- decreased birth weight / MGI
- palatal shelf hypoplasia / MGI
- palatal shelves fail to meet at midline / MGI
- hair follicle outer root sheath hyperplasia / MGI
- abnormal kidney mesenchyme morphology / MGI
- postnatal lethality, complete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- preweaning lethality, complete penetrance / MGI
- decreased nephron number / MGI
- absent metanephric mesenchyme / MGI
- short rostral-caudal axis / MGI
- small Meckel's cartilage / MGI
- abnormal lower incisor morphology / MGI
- abnormal nasal septum cartilage morphology / MGI
- abnormal temporal bone petrous part morphology / MGI
- absent thyroid cartilage / MGI
- absent cricoid cartilage / MGI
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