- preweaning lethality, complete penetrance / IMPC
B6NCrl;B6N-Atm1Brd Tdgf1tm1a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:12813 |
Citation information | RRID:IMSR_EM:12813 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 Tdgf1tm1a(EUCOMM)Hmgu/Ieg |
Alternative name | HEPD0737_8_E09 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Tdgf1tm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Cripto |
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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Provider affiliation | Institute of Experimental Genetics, Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH) |
Genetic information | This mouse line originates from EUCOMM ES clone HEPD0737_8_E09. 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 | Helmholtz Zentrum Muenchen - German Research Center for Environmental Health (GmbH), Oberschleißheim, Germany |
Animals used for archiving | heterozygous C57BL/6N 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
- Septopreoptic holoprosencephaly / Orphanet_280195
- Semilobar holoprosencephaly / Orphanet_220386
- Lobar holoprosencephaly / Orphanet_93924
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal heart morphology / MGI
- abnormal heart development / MGI
- absent notochord / MGI
- abnormal germ layer development / MGI
- abnormal mesoderm development / MGI
- absent mesoderm / MGI
- abnormal endoderm development / MGI
- failure of primitive streak formation / MGI
- abnormal gastrulation / MGI
- abnormal embryo turning / MGI
- absent vitelline blood vessels / MGI
- embryonic growth arrest / MGI
- premature death / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal extraembryonic tissue morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal primitive streak formation / MGI
- abnormal chorion morphology / MGI
- abnormal cell adhesion / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- absent prechordal plate / MGI
- abnormal amnion morphology / MGI
- holoprosencephaly / MGI
- cyclopia / MGI
- abnormal rostral-caudal axis patterning / MGI
- embryo phenotype / MGI
- absent somites / MGI
- abnormal mesendoderm development / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal visceral endoderm morphology / MGI
- abnormal visceral yolk sac blood island morphology / MGI
- abnormal neural fold morphology / MGI
- decreased fibroblast proliferation / MGI
- fused somites / MGI
- decreased midbrain size / MGI
- decreased forebrain size / MGI
- rostral body truncation / MGI
- short rostral-caudal axis / MGI
- absent anterior definitive endoderm / MGI
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