- increased monocyte cell number / IMPC
- abnormal auditory brainstem response / IMPC
- small superior vagus ganglion / IMPC
- small testis / IMPC
- decreased lean body mass / IMPC
- decreased total retina thickness / IMPC
- increased circulating phosphate level / IMPC
- decreased circulating serum albumin level / IMPC
- decreased prepulse inhibition / IMPC
- abnormal retina outer nuclear layer morphology / IMPC
- increased total body fat amount / IMPC
- abnormal startle reflex / IMPC
- male infertility / IMPC
- decreased startle reflex / IMPC
- increased neutrophil cell number / IMPC
- abnormal retina morphology / IMPC
- increased leukocyte cell number / IMPC
- increased lymphocyte cell number / IMPC
- decreased circulating total protein level / IMPC
- increased heart rate / IMPC
- female infertility / IMPC
- decreased locomotor activity / IMPC
- decreased lymphocyte cell number / IMPC
C57BL/6N-Sun1tm1a(EUCOMM)Wtsi/CipheOrl
Status | Available to order |
EMMA ID | EM:09532 |
Citation information | RRID:IMSR_EM:09532 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-Sun1tm1a(EUCOMM)Wtsi/CipheOrl |
Alternative name | EPD0325_5_F03 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Sun1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Sun1 |
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 | Centre d'ImmunoPhenomique - Ciphe |
Provider affiliation | Centre d |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0325_5_F03. 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 males |
Disease and phenotype information
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- small cerebellum / MGI
- abnormal cerebellum development / MGI
- abnormal cerebellar foliation / MGI
- abnormal cerebellum external granule cell layer morphology / MGI
- abnormal Purkinje cell morphology / MGI
- ectopic Purkinje cell / MGI
- small ovary / MGI
- small testis / MGI
- ataxia / MGI
- impaired coordination / MGI
- male infertility / MGI
- female infertility / MGI
- abnormal muscle morphology / MGI
- decreased brain weight / MGI
- absent ovarian follicles / MGI
- no phenotypic analysis / MGI
- abnormal cochlear outer hair cell morphology / MGI
- cochlear outer hair cell degeneration / MGI
- absent oocytes / MGI
- decreased testis weight / MGI
- decreased male germ cell number / MGI
- azoospermia / MGI
- abnormal female meiosis / MGI
- abnormal male meiosis / MGI
- absent pinna reflex / MGI
- abnormal spermatocyte morphology / MGI
- arrest of male meiosis / MGI
- absent cerebellum fissure / MGI
- abnormal chromosomal synapsis / MGI
- abnormal Purkinje cell migration / MGI
- increased or absent threshold for auditory brainstem response / MGI
- increased ovary apoptosis / MGI
- increased testis apoptosis / MGI
- abnormal meiotic attachment of telomere to nuclear envelope / MGI