- abnormal heart morphology / IMPC
- abnormal behavior / IMPC
- decreased thigmotaxis / IMPC
- enlarged spleen / IMPC
- abnormal spleen morphology / IMPC
- abnormal lymph node morphology / IMPC
- enlarged lymph nodes / IMPC
- abnormal eye morphology / IMPC
- hyperplasia / IMPC
- decreased anxiety-related response / IMPC
- small kidney / IMPC
- abnormal kidney morphology / IMPC
- increased heart atrium size / IMPC
- abnormal skin morphology / IMPC
- abnormal lung morphology / IMPC
- single kidney / IMPC
- enlarged kidney / IMPC
- decreased locomotor activity / IMPC
B10.Cg-Ncf1m1J H2q/Kctt
Status | Available to order |
EMMA ID | EM:01353 |
Citation information | RRID:IMSR_EM:01353 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 | B10.Cg-Ncf1m1J H2q/Kctt |
Alternative name | RHo-7 |
Strain type | Spontaneous |
Allele/Transgene symbol | Ncf1m1J, H2q |
Gene/Transgene symbol | Ncf1, H2 |
Information from provider
Provider | Rikard Holmdahl |
Provider affiliation | Lund University, CMB, Section for medical inflammation reseach |
Genetic information | The strain lacks expression of Ncf1 when homozygous for the mutation. The strain is based on The Jackson Laboratory's strain B6.Cg-Dock7m +/+ Leprdb/J (JAX stock ID 000697). However, this strain lacks the Lepr mutation, and basically only the Ncf1 gene remains from the original strain (minimal fragment). It is also backcrossed to C57BL/10.Q to a pure background (speed congenics). |
Phenotypic information | None. |
Breeding history | Backcrossed to B10.Q for more than 10 generations by speed congenics. |
References |
|
Information from EMMA
Archiving centre | Karolinska Institutet, Stockholm, Sweden |
Stage of embryos | 2-cell |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Chronic granulomatous disease / Orphanet_379
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased hematocrit / MGI
- abnormal liver physiology / MGI
- abnormal T cell differentiation / MGI
- increased susceptibility to bacterial infection / MGI
- abnormal immunoglobulin level / MGI
- increased IgM level / MGI
- abnormal cytokine secretion / MGI
- thyroid inflammation / MGI
- increased autoantibody level / MGI
- insulitis / MGI
- increased susceptibility to autoimmune diabetes / MGI
- decreased susceptibility to autoimmune diabetes / MGI
- decreased susceptibility to parasitic infection / MGI
- immune system phenotype / MGI
- periinsulitis / MGI
- abnormal T cell number / MGI
- decreased CD4-positive, alpha beta T cell number / MGI
- increased CD8-positive, alpha-beta T cell number / MGI
- decreased IgG1 level / MGI
- decreased IgG2a level / MGI
- increased physiological sensitivity to xenobiotic / MGI
- decreased physiological sensitivity to xenobiotic / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- abnormal angiogenesis / MGI
- abnormal heart morphology / MGI
- altered response to myocardial infarction / MGI
- abnormal lung morphology / MGI
- skin lesions / MGI
- abnormal spatial learning / MGI
- reduced long term potentiation / MGI
- abnormal cardiovascular system physiology / MGI
- cardiac hypertrophy / MGI
- abnormal postnatal growth / MGI
- abnormal inflammatory response / MGI
- abnormal respiratory system physiology / MGI
- abnormal tracheal smooth muscle morphology / MGI
- increased susceptibility to infection / MGI
- decreased susceptibility to viral infection / MGI
- abnormal macrophage physiology / MGI
- abnormal neutrophil physiology / MGI
- granulomatous inflammation / MGI
- dilated heart left ventricle / MGI
- increased systemic arterial blood pressure / MGI
- abnormal bile duct morphology / MGI
- abnormal cardiac muscle contractility / MGI
- enhanced long term potentiation / MGI
- decreased vasoconstriction / MGI
- increased angiotensin I-converting enzyme activity / MGI
- abnormal locomotor activation / MGI
- liver abscess / MGI
- increased circulating renin level / MGI
- abnormal intestinal goblet cell morphology / MGI
- oxidative stress / MGI
- abnormal vascular endothelial cell physiology / MGI
- abnormal vascular wound healing / MGI
- abnormal response to infection / MGI
- impaired granulocyte bactericidal activity / MGI
- increased acute inflammation / MGI
- immune system phenotype / MGI
- abnormal vascular smooth muscle physiology / MGI
- impaired cued conditioning behavior / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- increased lung compliance / MGI
- decreased airway resistance / MGI
Literature references
- Enhanced autoimmunity, arthritis, and encephalomyelitis in mice with a reduced oxidative burst due to a mutation in the Ncf1 gene.;Hultqvist Malin, Olofsson Peter, Holmberg Jens, Bäckström B Thomas, Tordsson Jesper, Holmdahl Rikard, ;2004;Proceedings of the National Academy of Sciences of the United States of America;101;12646-51; 15310853
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