Gene symbol | Rank | Alignment Length (aa) | Similarity % | Identity % | Method Count | Method Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD |
---|---|---|---|---|---|---|
Cep85l | 1 | 859 | 50 | 33 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
Species | Gene | Association | Disease Qualifier | Disease | Evidence | Source | Based On | References |
---|---|---|---|---|---|---|---|---|
No records match query. Try removing filters. |
Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_051340.1:g.146380542A>G | variant | SNP
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NC_051340.1:g.146387754T>C | variant | SNP
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NC_051340.1:g.146392003G>A | variant | SNP
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NC_051340.1:g.146400582T>C | variant | SNP
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NC_051340.1:g.146359119T>A | variant | SNP
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NC_051340.1:g.146401244A>G | variant | SNP
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NC_051340.1:g.146402663G>A | variant | SNP
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NC_051340.1:g.146399009T>C | variant | SNP
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NC_051340.1:g.146359761C>T | variant | SNP
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NC_051340.1:g.146402493C>T | variant | SNP
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