- abnormal snout morphology / IMPC
- abnormal gait / IMPC
- hypoplasia / IMPC
- process of degenerative change / IMPC
- abnormal eye size / IMPC
- decreased body weight / IMPC
- abnormal humerus morphology / IMPC
- excessive tearing / IMPC
- abnormal joint morphology / IMPC
- synechia / IMPC
- preweaning lethality, incomplete penetrance / IMPC
- abnormal cornea morphology / IMPC
- developmental and structural abnormality / IMPC
- abnormal response to new environment / IMPC
- abnormal cranium morphology / IMPC
- abnormal tooth morphology / IMPC
C57BL/6N-Nsun2tm1c(EUCOMM)Wtsi/WtsiOulu
Status | Available to order |
EMMA ID | EM:11650 |
International strain name | C57BL/6N-Nsun2tm1c(EUCOMM)Wtsi/WtsiOulu |
Alternative name | EPD0105_2_F10 |
Strain type | Targeted Mutant Strains : Targeted Conditional |
Allele/Transgene symbol | Nsun2tm1c(EUCOMM)Wtsi |
Gene/Transgene symbol | Nsun2 |
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 line originates from EUCOMM ES clone EPD0105_2_F10, after breeding with a Flp recombinase deleter line to convert the original targeted allele tm1a (knock-out first allele) into a conditional allele tm1c. 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 | University of Oulu, Oulu, Finland |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Autosomal recessive non-syndromic intellectual disability / Orphanet_88616
- Dubowitz syndrome / Orphanet_235
IMPC phenotypes (gene matching)
MGI phenotypes (gene matching)
- decreased bone mineral density / MGI
- abnormal rib morphology / MGI
- kyphosis / MGI
- lordosis / MGI
- decreased circulating LDL cholesterol level / MGI
- decreased circulating HDL cholesterol level / MGI
- alopecia / MGI
- abnormal hair cycle / MGI
- abnormal cranium morphology / MGI
- abnormal snout morphology / MGI
- abnormal liver physiology / MGI
- abnormal forebrain morphology / MGI
- abnormal dorsal root ganglion morphology / MGI
- small superior cervical ganglion / MGI
- abnormal testis morphology / MGI
- abnormal epidermis stratum basale morphology / MGI
- decreased body length / MGI
- decreased body weight / MGI
- decreased body size / MGI
- abnormal lens morphology / MGI
- cataract / MGI
- abnormal cornea morphology / MGI
- hyperactivity / MGI
- male infertility / MGI
- abnormal tooth morphology / MGI
- abnormal fertility/fecundity / MGI
- abnormal thymus capsule morphology / MGI
- decreased mean corpuscular volume / MGI
- oligozoospermia / MGI
- decreased circulating free fatty acid level / MGI
- abnormal joint morphology / MGI
- increased erythrocyte cell number / MGI
- decreased circulating glycerol level / MGI
- abnormal eye muscle morphology / MGI
- decreased lean body mass / MGI
- retroesophageal right subclavian artery / MGI
- abnormal spine curvature / MGI
- abnormal optic stalk morphology / MGI
- abnormal optic cup morphology / MGI
- abnormal deltoid tuberosity morphology / MGI
- basisphenoid bone foramen / MGI
- fusion of vertebral arches / MGI
- absent stapedial artery / MGI
- decreased length of long bones / MGI
- increased energy expenditure / MGI
- decreased energy expenditure / MGI
- decreased circulating cholesterol level / MGI
- increased oxygen consumption / MGI
- improved glucose tolerance / MGI
- abnormal humerus morphology / MGI
- decreased percent body fat/body weight / MGI
- decreased circulating glucose level / MGI
- decreased mean corpuscular hemoglobin / MGI
- decreased circulating amylase level / MGI
- abnormal hair cycle anagen phase / MGI
- abnormal hair shedding / MGI
- thoracoschisis / MGI
- increased carbon dioxide production / MGI
- abnormal optic chiasm morphology / MGI
- decreased total body fat amount / MGI
- decreased grip strength / MGI
- decreased bone mineral content / MGI
- lethality, incomplete penetrance / MGI
- abnormal systemic artery morphology / MGI
- testis degeneration / MGI
- absent hypoglossal canal / MGI
- thin hypoglossal nerve / MGI
- absent hypoglossal nerve / MGI
- abnormal hypoglossal nerve topology / MGI
- absent segment of posterior cerebral artery / MGI
- ductus venosus stenosis / MGI
- subcutaneous edema / MGI
- trigeminal neuroma / MGI
- absent ductus venosus valve / MGI
- abnormal ductus venosus valve morphology / MGI
- thin motoric part of trigeminal nerve / MGI
- intraembryonal intestine elongation / MGI
- abnormal infrahyoid muscle connection / MGI
- reduced sympathetic cervical ganglion size / MGI
- persistent dorsal ophthalmic artery / MGI
- abnormal external carotid artery origin / MGI
- abnormal vertebral artery topology / MGI
- persistent trigeminal artery / MGI
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