Statements (32)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:gene
|
| gptkbp:alias |
gptkb:ATFB10
gptkb:IRK1 gptkb:KIR2.1 gptkb:LQT7 gptkb:HHF2 CMH7 |
| gptkbp:approvedBy |
gptkb:potassium_inwardly_rectifying_channel_subfamily_J_member_2
|
| gptkbp:approvedSymbol |
gptkb:KCNJ2
|
| gptkbp:associatedWith |
gptkb:Andersen-Tawil_syndrome
gptkb:Familial_atrial_fibrillation gptkb:Long_QT_syndrome_7 |
| gptkbp:Entrez_Gene_ID |
3759
ENSG00000123684 |
| gptkbp:function |
encodes a potassium channel protein
|
| gptkbp:HGNC_ID |
gptkb:HGNC:6054
|
| https://www.w3.org/2000/01/rdf-schema#label |
HGNC:6054
|
| gptkbp:locatedOnChromosome |
17
|
| gptkbp:location |
17q24.3
|
| gptkbp:locusType |
gptkb:gene
gene with protein product |
| gptkbp:OMIM |
600681
|
| gptkbp:previousSymbols |
gptkb:IRK1
gptkb:HHF2 |
| gptkbp:proteinFamily |
gptkb:inwardly_rectifying_potassium_channels
gptkb:potassium_channels |
| gptkbp:RefSeq |
NM_000891
|
| gptkbp:species |
gptkb:Homo_sapiens
|
| gptkbp:symbol |
approved
|
| gptkbp:UniProtID |
P63252
|
| gptkbp:bfsParent |
gptkb:IMPDH1_gene
|
| gptkbp:bfsLayer |
7
|