- abnormal salivary gland morphology / IMPC
- increased circulating iron level / IMPC
- abnormal pancreas morphology / IMPC
- increased brain size / IMPC
- increased mean corpuscular hemoglobin / IMPC
- increased hemoglobin content / IMPC
- decreased body weight / IMPC
- decreased startle reflex / IMPC
- kyphosis / IMPC
- increased circulating alanine transaminase level / IMPC
- decreased heart rate / IMPC
- increased mean corpuscular volume / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- abnormal spine curvature / IMPC
- decreased locomotor activity / IMPC
- increased circulating aspartate transaminase level / IMPC
- abnormal brain morphology / IMPC
- abnormal skin morphology / IMPC
STOCK Bmp6tm1Rob/H
| Status | Available to order |
| EMMA ID | EM:02505 |
| Citation information | RRID:IMSR_EM:02505 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 | STOCK Bmp6tm1Rob/H |
| Alternative name | Bmp6 |
| Strain type | Targeted Mutant Strains : Knock-out |
| Allele/Transgene symbol | Bmp6tm1Rob |
| Gene/Transgene symbol | Bmp6 |
Information from provider
| Provider | Elizabeth Robertson |
| Provider affiliation | Sir William Dunn School of Pathology, University of Oxford |
| Genetic information | Mice carry a null mutation in Bmp6. Locus contains neo cassette. |
| Phenotypic information | Mice show no overt phenotype but can be used for studying the genetic redundancy of signally in the Bmp growth factor family. |
| Breeding history | Outcrossed onto CD1 background. |
| References |
|
| Homozygous fertile | yes |
| Homozygous viable | yes |
| Homozygous matings required | no |
| Immunocompromised | not known |
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
- Hemochromatosis type 5 / Orphanet_447792
IMPC phenotypes (gene matching)
Literature references
- Mice lacking Bmp6 function.;Solloway M J, Dudley A T, Bikoff E K, Lyons K M, Hogan B L, Robertson E J, ;1998;Developmental genetics;22;321-39; 9664685
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