- preweaning lethality, incomplete penetrance / IMPC
B6NCrl;B6N-Atm1Brd Cdontm1a(EUCOMM)Hmgu/Orl
Status | Available to order |
EMMA ID | EM:09568 |
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 |
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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