- preweaning lethality, complete penetrance / IMPC
B6NCrl;B6N-Atm1Brd Tdgf1tm1a(EUCOMM)Hmgu/Ieg
Status | Available to order |
EMMA ID | EM:12813 |
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:
|
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 |
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
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).