- abnormal heart morphology / IMPC
- enlarged heart / IMPC
- abnormal urinary bladder morphology / IMPC
- abnormal thymus morphology / IMPC
- small thymus / IMPC
- enlarged thymus / IMPC
- abnormal testis morphology / IMPC
- small testis / IMPC
- abnormal retina morphology / IMPC
- decreased exploration in new environment / IMPC
- abnormal seminal vesicle morphology / IMPC
- abnormal skin morphology / IMPC
- short tibia / IMPC
- increased NK cell number / IMPC
- enlarged urinary bladder / IMPC
- increased fasting circulating glucose level / IMPC
C57BL/6NCrl-Crxem1(IMPC)Ccpcz/Ph
Status | Available to order |
EMMA ID | EM:12278 |
International strain name | C57BL/6NCrl-Crxem1(IMPC)Ccpcz/Ph |
Alternative name | |
Strain type | Endonuclease-mediated |
Allele/Transgene symbol | Crxem1(IMPC)Ccpcz |
Gene/Transgene symbol | Crx |
Information from provider
Provider | Institute of Molecular Genetics |
Provider affiliation | Department of Transgenic Models of Diseases, Institute of Molecular Genetics |
Genetic information | This mouse line originates from CRISPR zygote microinjection. For further details see the project page at the IMPC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institute of Molecular Genetics, Prague, Czech Republic |
Animals used for archiving | heterozygous C57BL/6NCrl |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Cone rod dystrophy / Orphanet_1872
- Leber congenital amaurosis / Orphanet_65
- Retinitis pigmentosa / Orphanet_791
IMPC phenotypes (allele matching)
IMPC phenotypes (gene matching)
- enlarged thymus / IMPC
- increased fasting circulating glucose level / IMPC
- enlarged heart / IMPC
- abnormal thymus morphology / IMPC
- enlarged urinary bladder / IMPC
- abnormal testis morphology / IMPC
- small testis / IMPC
- abnormal heart morphology / IMPC
- abnormal urinary bladder morphology / IMPC
- abnormal skin morphology / IMPC
- increased NK cell number / IMPC
- abnormal retina morphology / IMPC
- short tibia / IMPC
- small thymus / IMPC
- decreased exploration in new environment / IMPC
- abnormal seminal vesicle morphology / IMPC
MGI phenotypes (gene matching)
- abnormal retinal photoreceptor morphology / MGI
- abnormal retinal cone cell morphology / MGI
- abnormal retina morphology / MGI
- blindness / MGI
- abnormal blood circulation / MGI
- abnormal ocular fundus morphology / MGI
- abnormal retinal layer morphology / MGI
- abnormal retinal photoreceptor layer morphology / MGI
- abnormal photoreceptor outer segment morphology / MGI
- abnormal photoreceptor inner segment morphology / MGI
- abnormal retinal outer nuclear layer morphology / MGI
- abnormal retinal outer plexiform layer morphology / MGI
- abnormal rod electrophysiology / MGI
- abnormal cone electrophysiology / MGI
- abnormal retinal pigmentation / MGI
- vision/eye phenotype / MGI
- abnormal eye electrophysiology / MGI
- abnormal horizontal cell morphology / MGI
- abnormal retinal bipolar cell morphology / MGI
- abnormal retinal rod bipolar cell morphology / MGI
- abnormal retinal cone bipolar cell morphology / MGI
- decreased retinal cone cell number / MGI
- retinal photoreceptor degeneration / MGI
- abnormal retinal rod cell outer segment morphology / MGI
- thin retinal outer nuclear layer / MGI
- retinal outer nuclear layer degeneration / MGI
- thin retinal outer plexiform layer / MGI
- short photoreceptor inner segment / MGI
- absent photoreceptor inner segment / MGI
- absent photoreceptor outer segment / MGI
- abnormal retinal blood vessel morphology / MGI
- abnormal retinal outer nuclear layer thickness / MGI
- abnormal electroretinogram waveform feature / MGI
- decreased a wave amplitude / MGI
- decreased b wave amplitude / MGI
- retinal spots / MGI
- abnormal circadian behavior / MGI
- delayed circadian behavior phase / MGI
Information on how we integrate external resources can be found here
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