- abnormal whole-body plethysmography / IMPC
- decreased circulating amylase level / IMPC
- atrophy / IMPC
- decreased defecation amount / IMPC
- decreased body weight / IMPC
- abnormal heart morphology / IMPC
- increased cellular hemoglobin content / IMPC
- decreased circulating triglyceride level / IMPC
- decreased body temperature / IMPC
- increased circulating potassium level / IMPC
- increased mean corpuscular volume / IMPC
- decreased locomotor activity / IMPC
- increased blood uric acid level / IMPC
- increased mean corpuscular hemoglobin concentration / IMPC
- enlarged heart / IMPC
C3;CAnN-Pde6brd1-3H/H
Status | Available to order |
EMMA ID | EM:01295 |
International strain name | C3;CAnN-Pde6brd1-3H/H |
Alternative name | atrd6 |
Strain type | Induced Mutant Strains : Chemically-induced |
Allele/Transgene symbol | Pde6brd1-3H |
Gene/Transgene symbol | Pde6b |
Information from provider
Provider | Caroline Thaung |
Provider affiliation | MRC Mammalian Genetics Unit |
Phenotypic information | Slow onset retinal degeneration. Homozygotes have retinal degeneration. Compound heterozygotes with Pdebrd1 in background have slightly faster disease |
References |
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Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
MGI allele-associated human disease models
Orphanet associated rare diseases, based on orthologous gene matching
- Retinitis pigmentosa / Orphanet_791
- Congenital stationary night blindness / Orphanet_215
IMPC phenotypes (gene matching)
MGI phenotypes (allele matching)
- retinal degeneration / MGI
MGI phenotypes (gene matching)
- abnormal retinal rod cell morphology / MGI
- abnormal retina morphology / MGI
- retinal degeneration / MGI
- decreased retinal photoreceptor cell number / MGI
- blindness / MGI
- abnormal retinal vasculature morphology / MGI
- abnormal ocular fundus morphology / MGI
- abnormal photoreceptor outer segment morphology / MGI
- abnormal retinal outer nuclear layer morphology / MGI
- abnormal rod electrophysiology / MGI
- abnormal cone electrophysiology / MGI
- vision/eye phenotype / MGI
- abnormal Muller cell morphology / MGI
- abnormal eye electrophysiology / MGI
- decreased visual acuity / MGI
- impaired pupillary reflex / MGI
- abnormal optic disk morphology / MGI
- retinal photoreceptor degeneration / MGI
- retinal rod cell degeneration / MGI
- absent retinal rod cells / MGI
- thin retinal outer nuclear layer / MGI
- retinal outer nuclear layer degeneration / MGI
- absent photoreceptor outer segment / MGI
- abnormal retinal blood vessel morphology / MGI
- decreased total retina thickness / MGI
Literature references
- Novel ENU-induced eye mutations in the mouse: models for human eye disease.;Thaung Caroline, West Katrine, Clark Brian J, McKie Lisa, Morgan Joanne E, Arnold Karen, Nolan Patrick M, Peters Jo, Hunter A Jackie, Brown Steve D M, Jackson Ian J, Cross Sally H, ;2002;Human molecular genetics;11;755-67; 11929848
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