- abnormal tibia morphology / IMPC
- abnormal femur morphology / IMPC
- abnormal autopod morphology / IMPC
- abnormal nail morphology / IMPC
- abnormal cornea morphology / IMPC
- abnormal digit morphology / IMPC
- abnormal joint morphology / IMPC
- vertebral transformation / IMPC
- polysyndactyly / IMPC
- fused phalanges / IMPC
- preweaning lethality, complete penetrance / IMPC
C57BL/6N-Pitx1em1(IMPC)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:11574 |
International strain name | C57BL/6N-Pitx1em1(IMPC)Wtsi/WtsiIeg |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Pitx1em1(IMPC)Wtsi |
Gene/Transgene symbol | Pitx1 |
Information from provider
Provider | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Familial clubfoot due to PITX1 point mutation / Orphanet_293150
- Brachydactyly-elbow wrist dysplasia syndrome / Orphanet_1275
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- abnormal tibia morphology / IMPC
- abnormal cornea morphology / IMPC
- polysyndactyly / IMPC
- abnormal digit morphology / IMPC
- abnormal joint morphology / IMPC
- fused phalanges / IMPC
- abnormal nail morphology / IMPC
- abnormal autopod morphology / IMPC
- abnormal femur morphology / IMPC
- vertebral transformation / IMPC
- preweaning lethality, complete penetrance / IMPC
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