C57BL/6N-Nptntm1a(EUCOMM)Hmgu/H

Status

Available to order

EMMA IDEM:06125
Citation informationRRID:IMSR_EM:06125 

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International strain nameC57BL/6N-Nptntm1a(EUCOMM)Hmgu/H
Alternative nameHEPD0633_1_A06
Strain typeTargeted Mutant Strains
Allele/Transgene symbolNptntm1a(EUCOMM)Hmgu
Gene/Transgene symbolNptn
DisclaimerPlease note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
  1. We can not guarantee a null mutation for Knock-out first alleles (tm1a alleles, see http://www.mousephenotype.org/about-ikmc/targeting-strategies) as the critical exon has not been deleted.
  2. That the structure of the targeted mutation in the ES cells obtained from EUCOMM/KOMP to generate EUCOMM/KOMP mice is not verified by INFRAFRONTIER/EMMA. It is recommended that the recipient confirms the mutation structure.
  3. No check for determining the copy number of the targeting construct in ES cells obtained from EUCOMM/KOMP is done by INFRAFRONTIER/EMMA.
  4. The level of quality control before mice are released is to confirm the individual mouse genotype by short range PCR.

Information from provider

Provider MRC, Medical Research Council
Provider affiliationMary Lyon Centre at MRC Harwell
Genetic informationThis mouse line originates from EUCOMM ES clone HEPD0633_1_A06. For further details on the construction of this clone see the page at the IMPC portal.
Phenotypic informationPotential phenotyping data in the IMPC portal
ReferencesNone available

Information from EMMA

Archiving centreMary Lyon Centre at MRC Harwell, Oxford, United Kingdom

Disease and phenotype information

IMPC phenotypes (gene matching)
  • decreased prepulse inhibition / IMPC
  • abnormal gait / IMPC
  • abnormal behavior / IMPC
  • increased circulating iron level / IMPC
  • hyperactivity / IMPC
  • abnormal iris morphology / IMPC
  • abnormal auditory brainstem response / IMPC
  • decreased anxiety-related response / IMPC
  • decreased total body fat amount / IMPC
  • increased circulating phosphate level / IMPC
  • limb grasping / IMPC
  • decreased thigmotaxis / IMPC
  • abnormal startle reflex / IMPC
  • decreased locomotor activity / IMPC
  • abnormal ear morphology / IMPC
  • increased mean corpuscular volume / IMPC
  • increased bone mineral content / IMPC
  • increased circulating cholesterol level / IMPC
  • tremors / IMPC
  • increased heart weight / IMPC
  • increased mean corpuscular hemoglobin / IMPC
  • increased hemoglobin content / IMPC
MGI phenotypes (gene matching)
  • trunk curl / MGI
  • impaired swimming / MGI
  • impaired righting response / MGI
  • abnormal CNS synaptic transmission / MGI
  • nervous system phenotype / MGI
  • decreased cochlear outer hair cell number / MGI
  • abnormal cochlear inner hair cell physiology / MGI
  • abnormal inner hair cell synaptic ribbon morphology / MGI
  • abnormal miniature excitatory postsynaptic currents / MGI
  • decreased CNS synapse formation / MGI
  • head tilt / MGI
  • impaired hearing / MGI
  • abnormal miniature inhibitory postsynaptic currents / MGI
  • abnormal dendritic spine morphology / MGI
  • increased or absent threshold for auditory brainstem response / MGI

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Genotyping protocol

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