C57BL/6N-Katnb1^{tm1a(EUCOMM)Hmgu}/Cnrm

Status	Available to order
EMMA ID	EM:06113
Citation information	RRID:IMSR_EM:06113 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/6N-Katnb1^{tm1a(EUCOMM)Hmgu}/Cnrm
Alternative name	HEPD0636_3_B09
Strain type	Targeted Mutant Strains
Allele/Transgene symbol	Katnb1^{tm1a(EUCOMM)Hmgu}
Gene/Transgene symbol	Katnb1
Disclaimer	Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA: 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. 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. No check for determining the copy number of the targeting construct in ES cells obtained from EUCOMM/KOMP is done by INFRAFRONTIER/EMMA. The level of quality control before mice are released is to confirm the individual mouse genotype by short range PCR.

Information from provider

Provider	CNR, Consiglio Nazionale delle Ricerche
Provider affiliation	EMMA-Monterotondo Campus International Development, CNR, Consiglio Nazionale delle Ricerche
Genetic information	This mouse line originates from EUCOMM ES clone HEPD0636_3_B09. 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	CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy

Disease and phenotype information

Orphanet associated rare diseases, based on orthologous gene matching

Lissencephaly syndrome, Norman-Roberts type / Orphanet_89844

IMPC phenotypes (gene matching)

preweaning lethality, complete penetrance / IMPC

MGI phenotypes (allele matching)

abnormal erythropoiesis / MGI
abnormal cell morphology / MGI
pale liver / MGI
decreased brain size / MGI
abnormal forebrain morphology / MGI
anophthalmia / MGI
microphthalmia / MGI
decreased embryo size / MGI
loss of cortex neurons / MGI
binucleate / MGI
aneuploidy / MGI
abnormal mitosis / MGI
small limb buds / MGI
abnormal neuronal precursor proliferation / MGI
decreased neuronal precursor cell number / MGI
holoprosencephaly / MGI
thin cerebral cortex / MGI
abnormal cortical ventricular zone morphology / MGI
abnormal mitotic spindle morphology / MGI
lethality throughout fetal growth and development, complete penetrance / MGI
decreased fibroblast proliferation / MGI
abnormal primary cilium morphology / MGI
abnormal embryo morphology / MGI
increased brain apoptosis / MGI

MGI phenotypes (gene matching)

abnormal erythropoiesis / MGI
abnormal cell morphology / MGI
pale liver / MGI
decreased brain size / MGI
abnormal forebrain morphology / MGI
small testis / MGI
anophthalmia / MGI
microphthalmia / MGI
decreased embryo size / MGI
male infertility / MGI
asthenozoospermia / MGI
globozoospermia / MGI
oligozoospermia / MGI
loss of cortex neurons / MGI
binucleate / MGI
aneuploidy / MGI
abnormal mitosis / MGI
small limb buds / MGI
abnormal neuronal precursor proliferation / MGI
decreased neuronal precursor cell number / MGI
holoprosencephaly / MGI
abnormal male meiosis / MGI
reproductive system phenotype / MGI
thin cerebral cortex / MGI
abnormal spermatid morphology / MGI
abnormal cortical ventricular zone morphology / MGI
abnormal sperm flagellum morphology / MGI
abnormal manchette morphology / MGI
abnormal mitotic spindle morphology / MGI
abnormal meiotic spindle morphology / MGI
abnormal sperm axoneme morphology / MGI
increased Sertoli cell phagocytosis / MGI
lethality throughout fetal growth and development, complete penetrance / MGI
decreased fibroblast proliferation / MGI
abnormal primary cilium morphology / MGI
abnormal embryo morphology / MGI
increased brain apoptosis / MGI

Information on how we integrate external resources can be found here

Order

Availabilities

Requesting frozen sperm or embryos is generally advisable wherever possible, in order to minimise the shipment of live mice.

Frozen sperm. Delivered in 4 weeks (after paperwork in place). €1740^*
Rederivation of mice from frozen stock, delivery time available upon request . €3880^*

Due to the dynamic nature of our processes strain availability may change at short notice. The local repository manager will advise you in these circumstances.

^* In addition users have to cover all the shipping costs (including the cost for returning dry-shippers, where applicable).

More details on pricing and delivery times

Practical information

Genotyping protocol

Example health report
(Current health report will be provided later)

Material Transfer Agreement (MTA)
Distribution of this strain is subject to a provider MTA. Both signing of the MTA and submission of the online EMMA Mutant Request Form are required before material can be shipped.

EMMA conditions
Legally binding conditions for the transfer

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C57BL/6N-Katnb1tm1a(EUCOMM)Hmgu/Cnrm