- decreased body weight / MGI
C57BL/6N-Atm1Brd Ripk4tm1a(EUCOMM)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:05792 |
Citation information | RRID:IMSR_EM:05792 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-Atm1Brd Ripk4tm1a(EUCOMM)Wtsi/WtsiOrl |
Alternative name | EPD0521_3_G01 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ripk4tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ripk4 |
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 EPD0521_3_G01. 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 | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac males |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Bartsocas-Papas syndrome / Orphanet_1234
- CHAND syndrome / Orphanet_1401
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- short limbs / MGI
- abnormal hindlimb morphology / MGI
- interdigital webbing / MGI
- short tail / MGI
- thick skin / MGI
- thick epidermis / MGI
- epidermal hyperplasia / MGI
- abnormal epidermis suprabasal layer morphology / MGI
- absent epidermis stratum corneum / MGI
- decreased body weight / MGI
- absent vibrissae / MGI
- abnormal vibrissa morphology / MGI
- abnormal tail morphology / MGI
- abnormal nose morphology / MGI
- abnormal keratinocyte differentiation / MGI
- anal atresia / MGI
- esophageal atresia / MGI
- parakeratosis / MGI
- craniofacial phenotype / MGI
- immune system phenotype / MGI
- hematopoietic system phenotype / MGI
- oral atresia / MGI
- abnormal skin appearance / MGI
- perinatal lethality, complete penetrance / MGI
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