- preweaning lethality, incomplete penetrance / IMPC
B6NCrl;B6N-Atm1Brd Cdontm1a(EUCOMM)Hmgu/Orl
Status | Available to order |
EMMA ID | EM:09568 |
Citation information | RRID:IMSR_EM:09568 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 | B6NCrl;B6N-Atm1Brd Cdontm1a(EUCOMM)Hmgu/Orl |
Alternative name | HEPD0610_4_C03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cdontm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Cdon |
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 | Institut de Transgenose, INTRAGENE |
Provider affiliation | TAAM-CDTA UPS44, Institut de Transgenose, INTRAGENE |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0610_4_C03. 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
Orphanet associated rare diseases, based on orthologous gene matching
- Alobar holoprosencephaly / Orphanet_93925
- Midline interhemispheric variant of holoprosencephaly / Orphanet_93926
- Microform holoprosencephaly / Orphanet_280200
- Pituitary stalk interruption syndrome / Orphanet_95496
- Septopreoptic holoprosencephaly / Orphanet_280195
- Semilobar holoprosencephaly / Orphanet_220386
- Lobar holoprosencephaly / Orphanet_93924
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal craniofacial morphology / MGI
- absent maxillary shelf / MGI
- domed cranium / MGI
- abnormal maxilla morphology / MGI
- weakness / MGI
- abnormal forebrain morphology / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal brain ventricle morphology / MGI
- decreased body size / MGI
- abnormal blood vessel morphology / MGI
- hydroencephaly / MGI
- hemorrhage / MGI
- premature death / MGI
- abnormal nose morphology / MGI
- abnormal premaxilla morphology / MGI
- nervous system phenotype / MGI
- abnormal craniofacial development / MGI
- small basisphenoid bone / MGI
- basisphenoid bone foramen / MGI
- abnormal maxillary shelf morphology / MGI
- absent upper incisors / MGI
- abnormal neuronal precursor proliferation / MGI
- holoprosencephaly / MGI
- thin cerebral cortex / MGI
- enlarged lateral ventricles / MGI
- abnormal palate development / MGI
- decreased maxillary shelf size / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- perinatal lethality, incomplete penetrance / MGI
- abnormal philtrum morphology / MGI
- absent lamina terminalis / MGI
- abnormal upper incisor morphology / MGI
- small nasal septum / MGI
- absent nasal septum cartilage / MGI
- nasal septum cartilage hypoplasia / MGI
- piriform aperture stenosis / MGI
- absent primary palate / MGI
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