- small ears / MGI
- lowered ear position / MGI
- belly spot / MGI
- decreased body size / MGI
- microphthalmia / MGI
- reduced female fertility / MGI
- coloboma / MGI
- embryonic lethality, complete penetrance / MGI
- absent snout / MGI
- anophthalmia / MGI
- decreased embryo size / MGI
- abnormal maxillary shelf morphology / MGI
- abnormal face development / MGI
C3H101H-Pax6Sey-H/H
Status | Available to order |
EMMA ID | EM:00437 |
International strain name | C3H101H-Pax6Sey-H/H |
Alternative name | Pax6{Sey-H} |
Strain type | Induced Mutant Strains : Radiation-induced |
Allele/Transgene symbol | Pax6Sey-H, |
Gene/Transgene symbol | Pax6 |
Information from provider
Provider | Jo Peters |
Provider affiliation | Institute of Hearing Research, MRC (Medical Research Council) |
Phenotypic information | Mice carrying the Pax6Sey-H mutation have small eyes. |
References | None available |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Isolated aniridia / Orphanet_250923
- Autosomal dominant keratitis / Orphanet_2334
- Coloboma of eyelid / Orphanet_98946
- Coloboma of optic disc / Orphanet_98947
- Peters anomaly / Orphanet_708
- Coloboma of iris / Orphanet_98944
- Coloboma of macula / Orphanet_98945
- Coloboma of choroid and retina / Orphanet_98942
- Isolated optic nerve hypoplasia/aplasia / Orphanet_137902
- Coloboma of eye lens / Orphanet_98943
- Foveal hypoplasia-presenile cataract syndrome / Orphanet_2253
- Aniridia-cerebellar ataxia-intellectual disability syndrome / Orphanet_1065
MGI phenotypes (allele matching)
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