C57BL/6N-Nrastm1a(EUCOMM)Hmgu/H
Status | Available to order |
EMMA ID | EM:10426 |
International strain name | C57BL/6N-Nrastm1a(EUCOMM)Hmgu/H |
Alternative name | HEPD0719_5_C04 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Nrastm1a(EUCOMM)Hmgu |
Gene/Transgene symbol | Nras |
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 HEPD0719_5_C04. For further details on the construction of this clone see the page at the IKMC 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 |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Large congenital melanocytic nevus / Orphanet_626
- RAS-associated autoimmune leukoproliferative disease / Orphanet_268114
- Juvenile myelomonocytic leukemia / Orphanet_86834
- Differentiated thyroid carcinoma / Orphanet_146
- Noonan syndrome / Orphanet_648
- Langerhans cell histiocytosis / Orphanet_389
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal leukocyte cell number / MGI
- decreased monocyte cell number / MGI
- increased granulocyte number / MGI
- pale liver / MGI
- abnormal thymus morphology / MGI
- decreased body weight / MGI
- weight loss / MGI
- postnatal growth retardation / MGI
- no abnormal phenotype detected / MGI
- no phenotypic analysis / MGI
- decreased spleen weight / MGI
- increased T cell number / MGI
- abnormal granulocyte differentiation / MGI
- preweaning lethality, complete penetrance / MGI
- chylous ascites / MGI
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