C57BL/6NTac-Ctsdtm1a(EUCOMM)Wtsi/Ics
Status | Available to order |
EMMA ID | EM:06216 |
International strain name | C57BL/6NTac-Ctsdtm1a(EUCOMM)Wtsi/Ics |
Alternative name | EPD0105_1_A12 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Ctsdtm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Ctsd |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
|
Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0105_1_A12. 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 | ICS, Institut Clinique de la Souris, Illkirch-Graffenstaden, France |
Animals used for archiving | heterozygous C57BL/6N Tac, wild-type C57BL/6N Tac |
Stage of embryos | 2-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- CLN10 disease / Orphanet_228337
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- abnormal microglial cell morphology / MGI
- abnormal hair cycle / MGI
- abnormal crypts of Lieberkuhn morphology / MGI
- abnormal intestinal mucosa morphology / MGI
- weakness / MGI
- hippocampal neuron degeneration / MGI
- decreased body weight / MGI
- abnormal retina morphology / MGI
- ataxia / MGI
- abnormal apoptosis / MGI
- thymus hypoplasia / MGI
- abnormal antigen presentation / MGI
- deafness / MGI
- blindness / MGI
- seizures / MGI
- premature death / MGI
- abnormal spleen white pulp morphology / MGI
- abnormal ileum morphology / MGI
- tonic seizures / MGI
- abnormal cochlear ganglion morphology / MGI
- neuron degeneration / MGI
- axonal dystrophy / MGI
- thymus atrophy / MGI
- decreased lymphocyte cell number / MGI
- abnormal thrombosis / MGI
- lysosomal protein accumulation / MGI
- decreased double-positive T cell number / MGI
- cachexia / MGI
- bradykinesia / MGI
- cellular phenotype / MGI
- retinal photoreceptor degeneration / MGI
- abnormal spleen B cell follicle morphology / MGI
- abnormal stomach wall morphology / MGI
- lethality at weaning, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
- increased or absent threshold for auditory brainstem response / MGI
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).