- decreased leukocyte cell number / IMPC
- abnormal head morphology / IMPC
- abnormal cranium morphology / IMPC
- decreased body weight / IMPC
- increased mean corpuscular volume / IMPC
- decreased erythrocyte cell number / IMPC
- decreased lean body mass / IMPC
- increased mean corpuscular hemoglobin / IMPC
- decreased bone mineral content / IMPC
- hypoplasia / IMPC
- hyperplasia / IMPC
- extramedullary hemopoiesis / IMPC
STOCK Cdk5rap2tm1a(EUCOMM)Wtsi/WtsiIeg
Status | Available to order |
EMMA ID | EM:05702 |
International strain name | STOCK Cdk5rap2tm1a(EUCOMM)Wtsi/WtsiIeg |
Alternative name | EPD0381_4_F01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cdk5rap2tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Cdk5rap2 |
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 | Wellcome Trust Sanger Institute |
Provider affiliation | Wellcome Trust Sanger Institute |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0381_4_F01. 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive primary microcephaly / Orphanet_2512
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- decreased body weight / IMPC
- decreased lean body mass / IMPC
- increased mean corpuscular volume / IMPC
- abnormal head morphology / IMPC
- hyperplasia / IMPC
- hypoplasia / IMPC
- decreased bone mineral content / IMPC
- extramedullary hemopoiesis / IMPC
- decreased leukocyte cell number / IMPC
- decreased erythrocyte cell number / IMPC
- increased mean corpuscular hemoglobin / IMPC
- abnormal cranium morphology / IMPC
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- kyphosis / MGI
- decreased leukocyte cell number / MGI
- abnormal erythropoiesis / MGI
- macrocytosis / MGI
- abnormal head morphology / MGI
- microcephaly / MGI
- abnormal cranium morphology / MGI
- decreased brain size / MGI
- abnormal cerebral cortex morphology / MGI
- abnormal spermatogenesis / MGI
- decreased body weight / MGI
- decreased body size / MGI
- anemia / MGI
- reduced fertility / MGI
- male infertility / MGI
- postnatal lethality / MGI
- premature death / MGI
- decreased germ cell number / MGI
- abnormal erythrocyte morphology / MGI
- increased mean corpuscular volume / MGI
- anisocytosis / MGI
- small olfactory bulb / MGI
- macrocytic anemia / MGI
- decreased erythrocyte cell number / MGI
- abnormal cell nucleus morphology / MGI
- increased neuron apoptosis / MGI
- abnormal forebrain development / MGI
- loss of cortex neurons / MGI
- abnormal plasma membrane morphology / MGI
- decreased lean body mass / MGI
- abnormal mitosis / MGI
- abnormal embryonic/fetal subventricular zone morphology / MGI
- premature hair loss / MGI
- cellular phenotype / MGI
- decreased oocyte number / MGI
- increased mean corpuscular hemoglobin / MGI
- thin cerebral cortex / MGI
- early cellular replicative senescence / MGI
- small hippocampus / MGI
- reticulocytopenia / MGI
- abnormal mitotic spindle morphology / MGI
- eye opacity / MGI
- abnormal neuron proliferation / MGI
- decreased bone mineral content / MGI
- enlarged brain ventricles / MGI
- increased ovary adenoma incidence / MGI
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