- 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 |
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'ImmunoPhenomique - Ciphe |
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 |
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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