- increased circulating glucose level / IMPC
- decreased locomotor activity / IMPC
- abnormal retina vasculature morphology / IMPC
- decreased hematocrit / IMPC
- abnormal auditory brainstem response / IMPC
- abnormal retina inner nuclear layer morphology / IMPC
- abnormal retina blood vessel morphology / IMPC
- decreased circulating HDL cholesterol level / IMPC
- persistence of hyaloid vascular system / IMPC
- decreased circulating cholesterol level / IMPC
- increased mean corpuscular volume / IMPC
- increased heart weight / IMPC
- decreased total retina thickness / IMPC
- increased mean corpuscular hemoglobin / IMPC
- decreased hemoglobin content / IMPC
- abnormal optic disk morphology / IMPC
- decreased erythrocyte cell number / IMPC
- increased startle reflex / IMPC
- decreased circulating triglyceride level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased circulating alkaline phosphatase level / IMPC
- increased fluid intake / IMPC
- decreased circulating total protein level / IMPC
- increased grip strength / IMPC
STOCK Dbnltm1a(KOMP)Wtsi/CipheOrl
Status | Available to order |
EMMA ID | EM:09624 |
Citation information | RRID:IMSR_EM:09624 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 Dbnltm1a(KOMP)Wtsi/CipheOrl |
Alternative name | EPD0504_4_A04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Dbnltm1a(KOMP)Wtsi |
Gene/Transgene symbol | Dbnl |
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 | Centre d'ImmunoPhenomique - Ciphe |
Provider affiliation | Centre d |
Genetic information | This mouse line originates from KOMP ES clone EPD0504_4_A04. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NCrl males |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- ruffled hair / MGI
- tremors / MGI
- paresis / MGI
- hindlimb paralysis / MGI
- convulsive seizures / MGI
- abnormal lung morphology / MGI
- decreased body weight / MGI
- impaired coordination / MGI
- limb grasping / MGI
- impaired swimming / MGI
- abnormal cardiovascular system physiology / MGI
- decreased IgM level / MGI
- abnormal T cell activation / MGI
- respiratory distress / MGI
- emphysema / MGI
- abnormal motor capabilities/coordination/movement / MGI
- abnormal T cell physiology / MGI
- decreased immunoglobulin level / MGI
- abnormal synaptic vesicle recycling / MGI
- increased spleen weight / MGI
- decreased T cell proliferation / MGI
- immune system phenotype / MGI
- reproductive system phenotype / MGI
- decreased IgG1 level / MGI
- decreased interleukin-2 secretion / MGI
- prenatal lethality, incomplete penetrance / MGI
- generalized edema / MGI
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