Statements (23)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:protein
|
| gptkbp:alsoKnownAs |
gptkb:SLC46A1
|
| gptkbp:associatedWith |
gptkb:hereditary_folate_malabsorption
|
| gptkbp:Entrez_Gene_ID |
ENSG00000141504
113235 |
| gptkbp:expressedIn |
gptkb:kidney
gptkb:small_intestine liver |
| gptkbp:fullName |
heme carrier protein 1
|
| gptkbp:function |
folate transporter
heme transporter |
| gptkbp:gene |
gptkb:SLC46A1
|
| https://www.w3.org/2000/01/rdf-schema#label |
HCP1
|
| gptkbp:locatedOnChromosome |
gptkb:chromosome_17
|
| gptkbp:location |
gptkb:cell_membrane
|
| gptkbp:mutationAssociatedWith |
causes hereditary folate malabsorption
|
| gptkbp:OMIM |
611672
|
| gptkbp:organism |
gptkb:Homo_sapiens
|
| gptkbp:transportation |
hemoglobin
folate |
| gptkbp:UniProtID |
Q96NT5
|
| gptkbp:bfsParent |
gptkb:SLC46A1
|
| gptkbp:bfsLayer |
7
|