Species | Gene symbol | Count | Best | Best reverse | Method Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN |
---|---|---|---|---|---|
Homo sapiens | PRAMEF13 | 3 of 10 | Yes | Yes | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF4 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF1 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF2 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF20 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF7 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF27 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF5 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF12 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF9 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF11 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF6 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF17 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF26 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF8 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF25 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF10 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF15 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF19 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF33 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Homo sapiens | PRAMEF18 | 3 of 10 | Yes | No | ☑☐☐☐☑☐☐☑☐☐ |
Rattus norvegicus | Pramef8-ps1 | 8 of 9 | Yes | Yes | ☑ ☑☑☑☐☑☑☑☑ |
Rattus norvegicus | Pramel36 | 8 of 9 | Yes | Yes | ☑ ☑☑☑☐☑☑☑☑ |
Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
---|---|---|---|---|---|---|---|
NC_000071.7:g.94761670C>T | variant | SNP
| |||||
NC_000071.7:g.94761362T>A | variant | SNP
| |||||
NC_000071.7:g.94761398G>A | variant | SNP
| |||||
NC_000071.7:g.94761655T>G | variant | SNP
| |||||
NC_000071.7:g.94763814C>T | variant | SNP
| |||||
NC_000071.7:g.94761098C>A | variant | SNP
| |||||
NC_000071.7:g.94762318G>A | variant | SNP
|