Gene symbol | Rank | Alignment Length (aa) | Similarity % | Identity % | Method Count | Method Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD |
---|---|---|---|---|---|---|
Chd1 | 1 | 1279 | 37 | 21 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd6 | 2 | 1306 | 34 | 21 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd2 | 3 | 1177 | 36 | 22 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Ercc6 | 4 | 1133 | 38 | 22 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Ercc6l | 5 | 1203 | 34 | 21 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd4 | 6 | 1170 | 35 | 22 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd5 | 7 | 1105 | 37 | 21 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Smarca4 | 8 | 1089 | 37 | 21 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd1l | 9 | 1028 | 38 | 23 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd3 | 10 | 1017 | 36 | 22 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Smarcal1 | 11 | 600 | 55 | 38 | 3 of 9 | ☑☐☐☐☐☐☑☑☐ |
Smarca2 | 12 | 924 | 38 | 24 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Smarca1 | 13 | 999 | 36 | 21 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd7 | 14 | 895 | 37 | 22 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Smarca5 | 15 | 845 | 39 | 23 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd9 | 16 | 712 | 39 | 24 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Btaf1 | 17 | 670 | 39 | 24 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Chd8 | 18 | 656 | 39 | 25 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Smarcad1 | 19 | 624 | 41 | 25 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Rad54b | 20 | 611 | 40 | 25 | 2 of 9 | ☑☐☐☐☐☐☐☑☐ |
Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
---|---|---|---|---|---|---|---|
NC_051348.1:g.39493488T>G | variant | SNP
| |||||
NC_051348.1:g.39441320G>A | variant | SNP
| |||||
NC_051348.1:g.39462224C>T | variant | SNP
| |||||
NC_051348.1:g.39463312A>G | variant | SNP
| |||||
NC_051348.1:g.39464015A>G | variant | SNP
| |||||
NC_051348.1:g.39465549T>G | variant | SNP
| |||||
NC_051348.1:g.39466224G>A | variant | SNP
| |||||
NC_051348.1:g.39466392G>A | variant | SNP
| |||||
NC_051348.1:g.39467416G>T | variant | SNP
| |||||
NC_051348.1:g.39479315T>A | variant | SNP
|