- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Katnb1tm1a(EUCOMM)Hmgu/Cnrm
Status | Available to order |
EMMA ID | EM:06113 |
International strain name | C57BL/6N-Katnb1tm1a(EUCOMM)Hmgu/Cnrm |
Alternative name | HEPD0636_3_B09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Katnb1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Katnb1 |
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 | 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)
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
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