- delayed bone ossification / MGI
- decreased compact bone thickness / MGI
- abnormal vertebral body morphology / MGI
- kyphosis / MGI
- scoliosis / MGI
- lordosis / MGI
- abnormal long bone hypertrophic chondrocyte zone / MGI
- megacephaly / MGI
- domed cranium / MGI
- abnormal small intestine morphology / MGI
- abnormal corpus callosum morphology / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal hippocampus morphology / MGI
- abnormal dentate gyrus morphology / MGI
- dilated lateral ventricles / MGI
- dilated third ventricle / MGI
- weight loss / MGI
- decreased body size / MGI
- delayed eyelid opening / MGI
- ataxia / MGI
- limb grasping / MGI
- hydroencephaly / MGI
- abnormal craniofacial bone morphology / MGI
- abnormal brain morphology / MGI
- no abnormal phenotype detected / MGI
- increased brain weight / MGI
- abnormal inner ear canal morphology / MGI
- abnormal cranial suture morphology / MGI
- abnormal bone mineralization / MGI
- abnormal long bone epiphyseal plate morphology / MGI
- delayed endochondral bone ossification / MGI
- abnormal long bone epiphyseal plate proliferative zone / MGI
- abnormal intervertebral disk morphology / MGI
- abnormal spine curvature / MGI
- intervertebral disk degeneration / MGI
- abnormal timing of postnatal eyelid opening / MGI
- craniofacial phenotype / MGI
- increased long bone epiphyseal plate size / MGI
- abnormal hippocampus CA1 region morphology / MGI
- slow postnatal weight gain / MGI
- enlarged lateral ventricles / MGI
- decreased trabecular bone thickness / MGI
- decreased trabecular bone mass / MGI
- lethality at weaning, incomplete penetrance / MGI
C57BL/6NTac-Nfixem6(IMPC)H/H
Status | Available to order |
EMMA ID | EM:12649 |
Citation information | RRID:IMSR_EM:12649 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-Nfixem6(IMPC)H/H |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Nfixem6(IMPC)H |
Gene/Transgene symbol | Nfix |
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
- Malan overgrowth syndrome / Orphanet_420179
- Marshall-Smith syndrome / Orphanet_561
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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