Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases associated to Myoc by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Juvenile Glaucoma | Ocular hypertension | ORPHA:98977 | |
Glaucoma 1, Open Angle, A | OMIM:137750 | ||
Congenital Glaucoma | ORPHA:98976 |
The table below shows human diseases predicted to be associated to Myoc by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Glaucoma 1, Primary Open Angle, C | Ocular hypertension | OMIM:601682 | |
Glaucoma 1, Open Angle, F | Ocular hypertension | OMIM:603383 | |
Glaucoma 3, Primary Congenital, E | Ocular hypertension | OMIM:617272 | |
Glaucoma 3, Primary Congenital, A | Ocular hypertension | OMIM:231300 | |
Microphthalmia, Isolated 6 | Ocular hypertension | OMIM:613517 | |
Microcoria, Congenital | Ocular hypertension | OMIM:156600 | |
Glaucoma, Primary Closed-Angle | Ocular hypertension | OMIM:618880 | |
Brachydactyly, Coloboma, And Anterior Segment Dysgenesis | Ocular hypertension | OMIM:610023 | |
Idiopathic Uveal Effusion Syndrome | Abnormal intraocular pressure | ORPHA:209956 | |
Irvan Syndrome | Ocular hypertension | ORPHA:209943 | |
Weill-Marchesani Syndrome 3 | Ocular hypertension | OMIM:614819 | |
Neovascular Glaucoma | Ocular hypertension | ORPHA:94058 | |
Birdshot Chorioretinopathy | Ocular hypertension | ORPHA:179 | |
Anterior Segment Dysgenesis 1 | Ocular hypertension | OMIM:107250 | |
Exfoliation Syndrome | Asymmetry of intraocular pressure | OMIM:177650 | |
Hyperostosis Cranialis Interna | Ocular hypertension | OMIM:144755 | |
Macrophthalmia, Colobomatous, With Microcornea | Ocular hypertension | OMIM:602499 | |
Anterior Segment Dysgenesis 7 | Ocular hypertension | OMIM:269400 | |
Uveal Melanoma | Ocular hypertension | ORPHA:39044 | |
Weill-Marchesani Syndrome 4 | Ocular hypertension | OMIM:613195 | |
1P31P32 Microdeletion Syndrome | Ocular hypertension | ORPHA:401986 | |
Craniofacial Anomalies And Anterior Segment Dysgenesis Syndrome | Ocular hypertension | OMIM:614195 | |
Juvenile Glaucoma | Ocular hypertension | ORPHA:98977 | |
Anterior Segment Dysgenesis 2 | Ocular hypertension | OMIM:610256 | |
Idiopathic Panuveitis | Ocular hypertension | ORPHA:280921 | |
Wagro Syndrome | Ocular hypertension | OMIM:612469 | |
Dural Sinus Malformation | Ocular hypertension | ORPHA:97339 | |
Posterior Polymorphous Corneal Dystrophy | Ocular hypertension | ORPHA:98973 | |
Musculocontractural Ehlers-Danlos Syndrome | Ocular hypertension | ORPHA:2953 | |
Late-Onset Retinal Degeneration | Ocular hypertension | ORPHA:67042 | |
Congenital Microcoria | Ocular hypertension | ORPHA:566 | |
Fuchs Heterochromic Iridocyclitis | Ocular hypertension | ORPHA:263479 | |
Nail-Patella Syndrome | Ocular hypertension | ORPHA:2614 | |
Diabetes Mellitus, Neonatal, With Congenital Hypothyroidism | Ocular hypertension | OMIM:610199 | |
Spondylometaphyseal Dysplasia, 'Corner Fracture' Type | Ocular hypertension | ORPHA:93315 | |
Facial Dysmorphism, Lens Dislocation, Anterior Segment Abnormalities, And Spontaneous Filtering Blebs | Ocular hypertension | OMIM:601552 | |
Oculoauricular Syndrome | Ocular hypertension | OMIM:612109 | |
Sympathetic Ophthalmia | Ocular hypertension | ORPHA:79098 | |
Phacoanaphylactic Uveitis | Ocular hypertension | ORPHA:209959 | |
Tubulointerstitial Nephritis And Uveitis Syndrome | Ocular hypertension | ORPHA:91500 | |
Glaucoma 1, Open Angle, A | OMIM:137750 | ||
Congenital Glaucoma | ORPHA:98976 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Myoctm1a(EUCOMM)Hmgu | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
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