Wikidata entity: Q14865150
| P1057 | chromosome | ... | Q847096 (human chromosome 11) | human chromosome 11 |
| P4196 | cytogenetic location | String | 11p15.5-p15.4 | ??? |
| P688 | encodes | ... | Q6449560 (Potassium voltage-gated channel subfamily Q member 1) | Potassium voltage-gated channel subfamily Q member 1 |
| P2888 | exact match | Url | None | ??? |
| P5572 | expressed in | ... | Q134955 (duodenum) | duodenum |
| P5572 | expressed in | ... | Q107244 (monocyte) | monocyte |
| P5572 | expressed in | ... | Q876089 (left ventricle) | left ventricle |
| P5572 | expressed in | ... | Q3270352 (body of stomach) | body of stomach |
| P5572 | expressed in | ... | Q4936946 (body of pancreas) | body of pancreas |
| P5572 | expressed in | ... | Q66502809 (apex of heart) | apex of heart |
| P5572 | expressed in | ... | Q66508047 (right lobe of thyroid gland) | right lobe of thyroid gland |
| P5572 | expressed in | ... | Q66508049 (left lobe of thyroid gland) | left lobe of thyroid gland |
| P5572 | expressed in | ... | Q66566695 (right adrenal cortex) | right adrenal cortex |
| P5572 | expressed in | ... | Q66566697 (left adrenal cortex) | left adrenal cortex |
| P703 | found in taxon | ... | Q15978631 (Homo sapiens) | Homo sapiens |
| P692 | Gene Atlas image | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20CD44%20204489%20s%20at%20fs.png | ??? |
| P692 | Gene Atlas image | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20CD44%20204490%20s%20at%20fs.png | ??? |
| P692 | Gene Atlas image | CommonsMedia | http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20CD44%20212063%20at%20fs.png | ??? |
| P2293 | genetic association | ... | Q653924 (long QT syndrome) | long QT syndrome |
| P2293 | genetic association | ... | Q724714 (Romano–Ward syndrome) | Romano–Ward syndrome |
| P2293 | genetic association | ... | Q1484058 (short QT syndrome) | short QT syndrome |
| P2293 | genetic association | ... | Q3025883 (type 2 diabetes) | type 2 diabetes |
| P2293 | genetic association | ... | Q3304152 (Jervell-Lange Nielsen syndrome) | Jervell-Lange Nielsen syndrome |
| P2293 | genetic association | ... | Q5432932 (familial atrial fibrillation) | familial atrial fibrillation |
| P645 | genomic end | String | 2870339 | ??? |
| P645 | genomic end | String | 2849105 | ??? |
| P644 | genomic start | String | 2444684 | ??? |
| P644 | genomic start | String | 2465914 | ??? |
| P593 | HomoloGene ID | String | 85014 | ??? |
| P31 | instance of | ... | Q7187 (gene) | gene |
| P684 | ortholog | ... | Q14865151 (Kcnq1) | Kcnq1 |
| P684 | ortholog | ... | Q24425205 (Kcnq1) | Kcnq1 |
| P684 | ortholog | ... | Q29659956 (kqt-3) | kqt-3 |
| P684 | ortholog | ... | Q29773399 (kcnq1.1) | kcnq1.1 |
| P2548 | strand orientation | ... | Q22809680 (forward strand) | forward strand |
| P279 | subclass of | ... | Q20747295 (protein-coding gene) | protein-coding gene |
| P594 | Ensembl gene ID | ENSG00000053918 |
| P594 | Ensembl gene ID | ENSG00000282076 |
| P704 | Ensembl transcript ID | ENST00000155840 |
| P704 | Ensembl transcript ID | ENST00000335475 |
| P704 | Ensembl transcript ID | ENST00000345015 |
| P704 | Ensembl transcript ID | ENST00000380776 |
| P704 | Ensembl transcript ID | ENST00000496887 |
| P704 | Ensembl transcript ID | ENST00000526095 |
| P704 | Ensembl transcript ID | ENST00000632153 |
| P704 | Ensembl transcript ID | ENST00000632981 |
| P704 | Ensembl transcript ID | ENST00000633370 |
| P704 | Ensembl transcript ID | ENST00000646564 |
| P351 | Entrez Gene ID | 3784 |
| P646 | Freebase ID | /m/05fpht |
| P353 | HGNC gene symbol | KCNQ1 |
| P354 | HGNC ID | 6294 |
| P8408 | KBpedia ID | KvLQT1 |
| P6366 | Microsoft Academic ID (discontinued) | 60983044 |
| P492 | OMIM ID | 607542 |
| P492 | OMIM ID | 607542 |
| P639 | RefSeq RNA ID | NM_000218 |
| P639 | RefSeq RNA ID | NM_181797 |
| P639 | RefSeq RNA ID | NM_181798 |
| P2892 | UMLS CUI | C1416612 |
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log id: 1247970