Wikidata entity: Q14914141
| P1057 | chromosome | ... | Q668633 (human chromosome 3) | human chromosome 3 |
| P4196 | cytogenetic location | String | 3p22.2 | ??? |
| P688 | encodes | ... | Q6981561 (Sodium voltage-gated channel alpha subunit 11) | Sodium voltage-gated channel alpha subunit 11 |
| P2888 | exact match | Url | None | ??? |
| P5572 | expressed in | ... | Q9371 (spleen) | spleen |
| P5572 | expressed in | ... | Q9384 (testicle) | testicle |
| P5572 | expressed in | ... | Q213456 (gonad) | gonad |
| P5572 | expressed in | ... | Q776972 (trigeminal ganglion) | trigeminal ganglion |
| P5572 | expressed in | ... | Q1395415 (spinal ganglia) | spinal ganglia |
| P5572 | expressed in | ... | Q6135922 (sural nerve) | sural nerve |
| P5572 | expressed in | ... | Q28455175 (ventricular zone) | ventricular zone |
| P5572 | expressed in | ... | Q66502829 (right testis) | right testis |
| P5572 | expressed in | ... | Q66502830 (left testis) | left testis |
| P5572 | expressed in | ... | Q116529247 (buccal mucosa cell) | buccal mucosa cell |
| P703 | found in taxon | ... | Q15978631 (Homo sapiens) | Homo sapiens |
| P2293 | genetic association | ... | Q50349715 (hereditary sensory and autonomic neuropathy type 7) | hereditary sensory and autonomic neuropathy type 7 |
| P2293 | genetic association | ... | Q55784748 (familial episodic pain syndrome with predominantly lower limb involvement) | familial episodic pain syndrome with predominantly lower limb involvement |
| P2293 | genetic association | ... | Q55785424 (autosomal dominant hereditary sensory and autonomic neuropathy) | autosomal dominant hereditary sensory and autonomic neuropathy |
| P645 | genomic end | String | 38992052 | ??? |
| P645 | genomic end | String | 39052157 | ??? |
| P644 | genomic start | String | 38845764 | ??? |
| P644 | genomic start | String | 38887260 | ??? |
| P593 | HomoloGene ID | String | 8041 | ??? |
| P31 | instance of | ... | Q7187 (gene) | gene |
| P684 | ortholog | ... | Q14914142 (Scn11a) | Scn11a |
| P684 | ortholog | ... | Q24382075 (Scn11a) | Scn11a |
| P684 | ortholog | ... | Q29711938 (para) | para |
| P2548 | strand orientation | ... | Q22809711 (reverse strand) | reverse strand |
| P279 | subclass of | ... | Q20747295 (protein-coding gene) | protein-coding gene |
| P594 | Ensembl gene ID | ENSG00000168356 |
| P704 | Ensembl transcript ID | ENST00000302328 |
| P704 | Ensembl transcript ID | ENST00000444237 |
| P704 | Ensembl transcript ID | ENST00000456224 |
| P704 | Ensembl transcript ID | ENST00000665106 |
| P704 | Ensembl transcript ID | ENST00000668754 |
| P704 | Ensembl transcript ID | ENST00000674755 |
| P704 | Ensembl transcript ID | ENST00000674979 |
| P704 | Ensembl transcript ID | ENST00000675223 |
| P704 | Ensembl transcript ID | ENST00000675269 |
| P704 | Ensembl transcript ID | ENST00000675672 |
| P704 | Ensembl transcript ID | ENST00000675892 |
| P704 | Ensembl transcript ID | ENST00000676045 |
| P704 | Ensembl transcript ID | ENST00000676176 |
| P704 | Ensembl transcript ID | ENST00000676333 |
| P351 | Entrez Gene ID | 11280 |
| P646 | Freebase ID | /m/03bxypj |
| P353 | HGNC gene symbol | SCN11A |
| P354 | HGNC ID | 10583 |
| P6366 | Microsoft Academic ID (discontinued) | 2777776202 |
| P492 | OMIM ID | 604385 |
| P492 | OMIM ID | 604385 |
| P639 | RefSeq RNA ID | NM_001287223 |
| P639 | RefSeq RNA ID | NM_001349253 |
| P639 | RefSeq RNA ID | NM_014139 |
| P639 | RefSeq RNA ID | NR_164473 |
| P639 | RefSeq RNA ID | XM_011533321 |
| P639 | RefSeq RNA ID | XM_017005650 |
| P639 | RefSeq RNA ID | XM_017005651 |
| P639 | RefSeq RNA ID | XM_017005653 |
| P639 | RefSeq RNA ID | XM_047447378 |
| P2892 | UMLS CUI | C1419854 |
Why not click here or view trends?
log id: 2104250