- hemorrhage / IMPC
- abnormal blood vessel morphology / IMPC
- microphthalmia / IMPC
- prenatal lethality / IMPC
- abnormal vitelline vasculature morphology / IMPC
- decreased respiratory quotient / IMPC
- decreased fluid intake / IMPC
- embryonic growth retardation / IMPC
- edema / IMPC
- abnormal embryo development / IMPC
- abnormal embryo size / IMPC
- abnormal visceral yolk sac morphology / IMPC
- abnormal hindbrain morphology / IMPC
- abnormal head shape / IMPC
- abnormal embryo turning / IMPC
- unresponsive to tactile stimuli / IMPC
- abnormal head size / IMPC
- no spontaneous movement / IMPC
- abnormal eye morphology / IMPC
- preweaning lethality, complete penetrance / IMPC
- decreased food intake / IMPC
C57BL/6N-Phgdhem1(IMPC)Wtsi/WtsiCnbc
Status | Available to order |
EMMA ID | EM:13924 |
Citation information | RRID:IMSR_EM:13924 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 | C57BL/6N-Phgdhem1(IMPC)Wtsi/WtsiCnbc |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Phgdhem1(IMPC)Wtsi |
Gene/Transgene symbol | Phgdh |
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 | CNB-CSIC, Centro Nacional de Biotecnologia, Madrid, Spain |
Animals used for archiving | heterozygous C57BL/6N males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Neu-Laxova syndrome / Orphanet_2671
- 3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form / Orphanet_79351
- Neu-laxova syndrome due to 3-phosphoglycerate dehydrogenase deficiency / Orphanet_583607
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- interdigital webbing / MGI
- decreased brain size / MGI
- forebrain hypoplasia / MGI
- abnormal embryonic neuroepithelial layer differentiation / MGI
- absent cerebellum / MGI
- abnormal brain development / MGI
- exencephaly / MGI
- decreased embryo size / MGI
- absent olfactory bulb / MGI
- abnormal nervous system development / MGI
- abnormal embryonic/fetal subventricular zone morphology / MGI
- enlarged lateral ventricles / MGI
- abnormal neuron differentiation / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
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