- corneal vascularization / IMPC
- preweaning lethality, complete penetrance / IMPC
- increased circulating HDL cholesterol level / IMPC
- embryonic lethality prior to tooth bud stage / IMPC
- decreased locomotor activity / IMPC
- increased grip strength / IMPC
- increased circulating triglyceride level / IMPC
- abnormal startle reflex / IMPC
- increased large unstained cell number / IMPC
- increased circulating cholesterol level / IMPC
C57BL/6NTac-Nodaltm1a(EUCOMM)Wtsi/H
Status | Available to order |
EMMA ID | EM:10453 |
International strain name | C57BL/6NTac-Nodaltm1a(EUCOMM)Wtsi/H |
Alternative name | EPD0197_2_B12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Nodaltm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Nodal |
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 | MRC, Medical Research Council |
Provider affiliation | Mary Lyon Centre at MRC Harwell |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0197_2_B12. 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 | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | heterozygous C57BL/6NTac |
Breeding at archiving centre | This mutation was made on a coisogenic C57BL/6NTac background |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Situs inversus totalis / Orphanet_101063
- 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 development / MGI
- abnormal heart looping / MGI
- abnormal interventricular septum morphology / MGI
- enlarged pericardium / MGI
- trabecula carnea hypoplasia / MGI
- abnormal foregut morphology / MGI
- right-sided isomerism / MGI
- right pulmonary isomerism / MGI
- abnormal liver morphology / MGI
- small liver / MGI
- pale liver / MGI
- abnormal spleen morphology / MGI
- small spleen / MGI
- spleen hypoplasia / MGI
- abnormal brain development / MGI
- absent floor plate / MGI
- absent notochord / MGI
- decreased body size / MGI
- abnormal ectoderm development / MGI
- failure of primitive streak formation / MGI
- abnormal gastrulation / MGI
- decreased embryo size / MGI
- abnormal embryo turning / MGI
- abnormal left-right axis patterning / MGI
- absent amniotic folds / MGI
- embryonic growth arrest / MGI
- pericardial edema / MGI
- premature death / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal extraembryonic tissue morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal gastrulation movements / MGI
- abnormal primitive streak formation / MGI
- abnormal primitive streak morphology / MGI
- small ectoplacental cone / MGI
- situs ambiguus / MGI
- aortic hypertrophy / MGI
- no phenotypic analysis / MGI
- absent allantois / MGI
- abnormal digestive system development / MGI
- absent placental labyrinth / MGI
- abnormal craniofacial development / MGI
- thin myocardium compact layer / MGI
- abnormal primitive node morphology / MGI
- transposition of great arteries / MGI
- heterotaxia / MGI
- abnormal direction of heart looping / MGI
- abnormal spongiotrophoblast layer morphology / MGI
- abnormal embryonic neuroepithelium morphology / MGI
- abnormal prechordal plate morphology / MGI
- absent prechordal plate / MGI
- truncated notochord / MGI
- abnormal neural fold formation / MGI
- absent amnion / MGI
- holoprosencephaly / MGI
- abnormal rostral-caudal axis patterning / MGI
- embryo phenotype / MGI
- right atrial isomerism / MGI
- abnormal heart position or orientation / MGI
- abnormal extraembryonic mesoderm development / MGI
- absent somites / MGI
- abnormal anterior visceral endoderm morphology / MGI
- abnormal hindgut morphology / MGI
- abnormal mesendoderm development / MGI
- absent primitive node / MGI
- increased trophoblast giant cell number / MGI
- abnormal lateral plate mesoderm morphology / MGI
- atrial septal defect / MGI
- common atrium / MGI
- abnormal extraembryonic ectoderm morphology / MGI
- abnormal stomach position or orientation / MGI
- neonatal lethality, complete penetrance / MGI
- perinatal lethality, complete penetrance / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
- embryonic lethality between somite formation and embryo turning, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- embryonic lethality, incomplete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- abnormal visceral endoderm morphology / MGI
- abnormal parietal yolk sac morphology / MGI
- absent visceral yolk sac / MGI
- thin placenta labyrinth / MGI
- fused somites / MGI
- absent heart tube / MGI
- delayed heart development / MGI
- absent foregut / MGI
- truncated foregut / MGI
- absent midbrain / MGI
- increased spongiotrophoblast size / MGI
- embryonic-extraembryonic boundary constriction / MGI
- absent forebrain / MGI
- rostral body truncation / MGI
- abnormal head development / MGI
- abnormal heart apex morphology / MGI
- decreased embryonic neuroepithelial cell proliferation / MGI
- absent head fold / MGI
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