- decreased body weight / MGI
C57BL/6N-Atm1Brd Ripk4tm1a(EUCOMM)Wtsi/WtsiOrl
Status | Available to order |
EMMA ID | EM:05792 |
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/6N Tac |
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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