Wikidata entity: Q18043108
| P1057 | chromosome | ... | Q638893 (human chromosome 2) | human chromosome 2 |
| P4196 | cytogenetic location | String | 2q32.3 | ??? |
| P688 | encodes | ... | Q21118254 (HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2) | HECT, C2 and WW domain containing E3 ubiquitin protein ligase 2 |
| P2888 | exact match | Url | None | ??? |
| P5572 | expressed in | ... | Q9384 (testicle) | testicle |
| P5572 | expressed in | ... | Q3497796 (visceral pleura) | visceral pleura |
| P5572 | expressed in | ... | Q4973067 (Brodmann area 23) | Brodmann area 23 |
| P5572 | expressed in | ... | Q4973094 (Brodmann area 46) | Brodmann area 46 |
| P5572 | expressed in | ... | Q5407200 (middle temporal gyrus) | middle temporal gyrus |
| P5572 | expressed in | ... | Q5938041 (right lung) | right lung |
| P5572 | expressed in | ... | Q28656741 (upper lobe of lung) | upper lobe of lung |
| P5572 | expressed in | ... | Q28656761 (upper lobe of left lung) | upper lobe of left lung |
| P5572 | expressed in | ... | Q66504996 (myocardium of left ventricle) | myocardium of left ventricle |
| P5572 | expressed in | ... | Q66531315 (primary visual cortex) | primary visual cortex |
| P703 | found in taxon | ... | Q15978631 (Homo sapiens) | Homo sapiens |
| P2293 | genetic association | ... | Q55785166 (neurodevelopmental disorder with hypotonia, seizures, and absent language; NDHSAL) | neurodevelopmental disorder with hypotonia, seizures, and absent language; NDHSAL |
| P645 | genomic end | String | 196593684 | ??? |
| P645 | genomic end | String | 197458416 | ??? |
| P644 | genomic start | String | 196189099 | ??? |
| P644 | genomic start | String | 197059094 | ??? |
| P593 | HomoloGene ID | String | 66192 | ??? |
| P31 | instance of | ... | Q7187 (gene) | gene |
| P684 | ortholog | ... | Q18302547 (Hecw2) | Hecw2 |
| P684 | ortholog | ... | Q24395835 (Hecw2) | Hecw2 |
| P684 | ortholog | ... | Q29753878 (hecw2b) | hecw2b |
| P2548 | strand orientation | ... | Q22809711 (reverse strand) | reverse strand |
| P279 | subclass of | ... | Q20747295 (protein-coding gene) | protein-coding gene |
| P594 | Ensembl gene ID | ENSG00000138411 |
| P704 | Ensembl transcript ID | ENST00000260983 |
| P704 | Ensembl transcript ID | ENST00000427457 |
| P704 | Ensembl transcript ID | ENST00000462290 |
| P704 | Ensembl transcript ID | ENST00000498146 |
| P704 | Ensembl transcript ID | ENST00000642318 |
| P704 | Ensembl transcript ID | ENST00000642531 |
| P704 | Ensembl transcript ID | ENST00000642884 |
| P704 | Ensembl transcript ID | ENST00000644030 |
| P704 | Ensembl transcript ID | ENST00000644256 |
| P704 | Ensembl transcript ID | ENST00000644405 |
| P704 | Ensembl transcript ID | ENST00000644421 |
| P704 | Ensembl transcript ID | ENST00000644978 |
| P704 | Ensembl transcript ID | ENST00000645468 |
| P704 | Ensembl transcript ID | ENST00000645770 |
| P704 | Ensembl transcript ID | ENST00000647236 |
| P704 | Ensembl transcript ID | ENST00000647314 |
| P704 | Ensembl transcript ID | ENST00000647402 |
| P351 | Entrez Gene ID | 57520 |
| P646 | Freebase ID | /m/0125ykg7 |
| P353 | HGNC gene symbol | HECW2 |
| P354 | HGNC ID | 29853 |
| P492 | OMIM ID | 617245 |
| P492 | OMIM ID | 617245 |
| P639 | RefSeq RNA ID | NM_001304840 |
| P639 | RefSeq RNA ID | NM_001348768 |
| P639 | RefSeq RNA ID | NM_020760 |
| P639 | RefSeq RNA ID | XM_006712646 |
| P639 | RefSeq RNA ID | XM_006712648 |
| P639 | RefSeq RNA ID | XM_024453020 |
| P639 | RefSeq RNA ID | XM_024453021 |
| P639 | RefSeq RNA ID | XM_047445194 |
| P639 | RefSeq RNA ID | XM_047445195 |
| P639 | RefSeq RNA ID | XM_047445196 |
| P639 | RefSeq RNA ID | XM_047445197 |
| P639 | RefSeq RNA ID | XM_047445198 |
| P2892 | UMLS CUI | C1539660 |
Why not click here or view trends?
log id: 5202557