- 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 |
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 |
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
Information on how we integrate external resources can be found here
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