Statements (65)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:associatedWith |
gptkb:Tangier_disease
gptkb:familial_high-density_lipoprotein_deficiency |
| gptkbp:encodes |
gptkb:ATP-binding_cassette_sub-family_A_member_1
|
| gptkbp:Entrez_Gene_ID |
19
|
| gptkbp:geneType |
protein-coding
|
| gptkbp:hasTranscript |
gptkb:ENST00000544455
ENST00000263253 ENST00000544456 ENST00000544457 ENST00000544458 ENST00000544459 ENST00000544460 ENST00000544461 ENST00000544462 ENST00000544463 ENST00000544464 ENST00000544465 ENST00000544466 ENST00000544467 ENST00000544468 ENST00000544469 ENST00000544470 ENST00000544471 ENST00000544472 ENST00000544473 ENST00000544474 ENST00000544475 ENST00000544476 ENST00000544477 ENST00000544478 ENST00000544479 ENST00000544480 ENST00000544481 ENST00000544482 ENST00000544483 ENST00000544484 ENST00000544485 ENST00000544486 ENST00000544487 ENST00000544488 ENST00000544489 ENST00000544490 ENST00000544491 ENST00000544492 ENST00000544493 ENST00000544494 ENST00000544495 ENST00000544496 ENST00000544497 ENST00000544498 ENST00000544499 ENST00000544500 |
| gptkbp:HGNC_ID |
gptkb:HGNC:29
|
| https://www.w3.org/2000/01/rdf-schema#label |
ENSG00000102974
|
| gptkbp:locatedOnChromosome |
chromosome 1
|
| gptkbp:OMIM |
600046
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:startPoint |
10606737
10736634 |
| gptkbp:strand |
plus
|
| gptkbp:symbol |
gptkb:ABCA1
|
| gptkbp:UniProtID |
gptkb:O95477
|
| gptkbp:bfsParent |
gptkb:CTCF
|
| gptkbp:bfsLayer |
8
|