Wikidata entity: Q14905729

| P1057 | chromosome | ... | Q668633 (human chromosome 3) | human chromosome 3 |
| P4196 | cytogenetic location | String | 3p22.2 | ??? |
| P688 | encodes | ... | Q3459294 (Sodium voltage-gated channel alpha subunit 5) | Sodium voltage-gated channel alpha subunit 5 |
| P2888 | exact match | Url | None | ??? |
| P5572 | expressed in | ... | Q9384 (testicle) | testicle |
| P5572 | expressed in | ... | Q213456 (gonad) | gonad |
| P5572 | expressed in | ... | Q6135922 (sural nerve) | sural nerve |
| P5572 | expressed in | ... | Q876089 (left ventricle) | left ventricle |
| P5572 | expressed in | ... | Q1308310 (right ventricle) | right ventricle |
| P5572 | expressed in | ... | Q66502809 (apex of heart) | apex of heart |
| P5572 | expressed in | ... | Q66502834 (right auricle of heart) | right auricle of heart |
| P5572 | expressed in | ... | Q66502871 (cardiac muscle tissue of right atrium) | cardiac muscle tissue of right atrium |
| P5572 | expressed in | ... | Q66504996 (myocardium of left ventricle) | myocardium of left ventricle |
| P5572 | expressed in | ... | Q66509944 (secondary oocyte) | secondary oocyte |
| P703 | found in taxon | ... | Q15978631 (Homo sapiens) | Homo sapiens |
| P2293 | genetic association | ... | Q189331 (heart arrhythmia) | heart arrhythmia |
| P2293 | genetic association | ... | Q161801 (sudden infant death syndrome) | sudden infant death syndrome |
| P2293 | genetic association | ... | Q724714 (Romano–Ward syndrome) | Romano–Ward syndrome |
| P2293 | genetic association | ... | Q815819 (atrial fibrillation) | atrial fibrillation |
| P2293 | genetic association | ... | Q1361515 (heart conduction disease) | heart conduction disease |
| P2293 | genetic association | ... | Q27677682 (Brugada syndrome 1) | Brugada syndrome 1 |
| P2293 | genetic association | ... | Q28024556 (dilated cardiomyopathy 1E) | dilated cardiomyopathy 1E |
| P2293 | genetic association | ... | Q32139750 (long QT syndrome 3) | long QT syndrome 3 |
| P2293 | genetic association | ... | Q32146767 (progressive familial heart block) | progressive familial heart block |
| P2293 | genetic association | ... | Q55783351 (idiopathic ventricular fibrillation, non Brugada type) | idiopathic ventricular fibrillation, non Brugada type |
| P645 | genomic end | String | 38649687 | ??? |
| P645 | genomic end | String | 38691164 | ??? |
| P644 | genomic start | String | 38548057 | ??? |
| P644 | genomic start | String | 38589548 | ??? |
| P593 | HomoloGene ID | String | 22738 | ??? |
| P31 | instance of | ... | Q7187 (gene) | gene |
| P684 | ortholog | ... | Q14905730 (Scn5a) | Scn5a |
| P684 | ortholog | ... | Q24381410 (Scn5a) | Scn5a |
| P684 | ortholog | ... | Q29711938 (para) | para |
| P684 | ortholog | ... | Q29749344 (scn12aa) | scn12aa |
| P684 | ortholog | ... | Q29763502 (scn5lab) | scn5lab |
| P2548 | strand orientation | ... | Q22809711 (reverse strand) | reverse strand |
| P279 | subclass of | ... | Q20747295 (protein-coding gene) | protein-coding gene |
| P594 | Ensembl gene ID | ENSG00000183873 |
| P704 | Ensembl transcript ID | ENST00000327956 |
| P704 | Ensembl transcript ID | ENST00000333535 |
| P704 | Ensembl transcript ID | ENST00000413689 |
| P704 | Ensembl transcript ID | ENST00000414099 |
| P704 | Ensembl transcript ID | ENST00000423572 |
| P704 | Ensembl transcript ID | ENST00000449557 |
| P704 | Ensembl transcript ID | ENST00000450102 |
| P704 | Ensembl transcript ID | ENST00000455624 |
| P704 | Ensembl transcript ID | ENST00000464652 |
| P704 | Ensembl transcript ID | ENST00000476683 |
| P704 | Ensembl transcript ID | ENST00000491944 |
| P351 | Entrez Gene ID | 6331 |
| P646 | Freebase ID | /m/0h050j |
| P353 | HGNC gene symbol | SCN5A |
| P354 | HGNC ID | 10593 |
| P6366 | Microsoft Academic ID (discontinued) | 2776250582 |
| P492 | OMIM ID | 600163 |
| P492 | OMIM ID | 600163 |
| P10283 | OpenAlex ID | C2776250582 |
| P639 | RefSeq RNA ID | NM_000335 |
| P639 | RefSeq RNA ID | NM_001099404 |
| P639 | RefSeq RNA ID | NM_001099405 |
| P639 | RefSeq RNA ID | NM_001160160 |
| P639 | RefSeq RNA ID | NM_001160161 |
| P639 | RefSeq RNA ID | NM_001354701 |
| P639 | RefSeq RNA ID | NM_198056 |
| P639 | RefSeq RNA ID | XM_011533991 |
| P2892 | UMLS CUI | C1419864 |
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log id: 3049061