- increased body length / IMPC
- abnormal behavior / IMPC
- decreased mean corpuscular hemoglobin / IMPC
- decreased circulating glucose level / IMPC
- process of degenerative change / IMPC
- increased circulating alkaline phosphatase level / IMPC
- hypoplasia / IMPC
- decreased circulating HDL cholesterol level / IMPC
- decreased circulating cholesterol level / IMPC
- increased lean body mass / IMPC
- decreased circulating LDL cholesterol level / IMPC
- decreased mean corpuscular volume / IMPC
- decreased hemoglobin content / IMPC
C57BL/6NTac-Sqstm1em1H/H
Status | Available to order |
EMMA ID | EM:14650 |
Citation information | RRID:IMSR_EM:14650 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-Sqstm1em1H/H |
Alternative name | SQSTM1-G331D-EM1-B6N |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Sqstm1em1H |
Gene/Transgene symbol | Sqstm1 |
Information from provider
Provider | MRC-Harwell |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | For detailed information on the genetic description of this strain, please have a look at this report. |
Phenotypic information | Homozygous:not knownHeterozygous:None reported |
Breeding history | Co-isogenic on original background |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | not known |
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
- Amyotrophic lateral sclerosis / Orphanet_803
- Frontotemporal dementia with motor neuron disease / Orphanet_275872
- Behavioral variant of frontotemporal dementia / Orphanet_275864
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal trabecular bone morphology / MGI
- kyphosis / MGI
- lordosis / MGI
- increased body length / MGI
- increased body weight / MGI
- abnormal osteoclast physiology / MGI
- hyperglycemia / MGI
- premature death / MGI
- abnormal bone mineralization / MGI
- increased susceptibility to age related obesity / MGI
- oxidative stress / MGI
- premature aging / MGI
- abnormal bone structure / MGI
- abnormal compact bone morphology / MGI
- abnormal behavior / MGI
- abnormal osteoclast morphology / MGI
- increased osteoclast cell number / MGI
- decreased osteoclast cell number / MGI
- decreased oxygen consumption / MGI
- impaired glucose tolerance / MGI
- skeleton phenotype / MGI
- decreased circulating glucose level / MGI
- decreased mean corpuscular hemoglobin / MGI
- increased circulating leptin level / MGI
- abnormal mitochondrial physiology / MGI
- abnormal bone ossification / MGI
- abnormal osteoclast differentiation / MGI
- decreased interleukin-6 secretion / MGI
- decreased subcutaneous adipose tissue amount / MGI
- increased neuron number / MGI
- rough coat / MGI
- abnormal respiratory electron transport chain / MGI
- abnormal aerobic respiration / MGI
- increased food intake / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).