|
gptkbp:instanceOf
|
gptkb:protein
|
|
gptkbp:alternativeName
|
gptkb:OCTN2
|
|
gptkbp:associatedWith
|
primary systemic carnitine deficiency
|
|
gptkbp:biologicalProcess
|
transmembrane transporter activity
carnitine transport
|
|
gptkbp:cellularComponent
|
integral component of plasma membrane
|
|
gptkbp:Entrez_Gene_ID
|
gptkb:ENSP00000361322
6584
|
|
gptkbp:function
|
carnitine transporter
|
|
gptkbp:gene
|
gptkb:SLC22A5
|
|
gptkbp:GO_term
|
GO:0005886
GO:0015293
GO:0006865
|
|
gptkbp:HGNC_ID
|
11057
|
|
gptkbp:KEGGID
|
hsa:6584
|
|
gptkbp:length
|
557
|
|
gptkbp:locatedOnChromosome
|
5q31
|
|
gptkbp:molecularWeight
|
63000
|
|
gptkbp:OMIM
|
603377
|
|
gptkbp:organism
|
gptkb:Homo_sapiens
|
|
gptkbp:protein_name
|
gptkb:Solute_carrier_family_22_member_5
|
|
gptkbp:proteinFamily
|
PF13520
|
|
gptkbp:Reactome
|
R-HSA-425393
|
|
gptkbp:RefSeq
|
NP_003049.2
|
|
gptkbp:subcellularLocation
|
gptkb:plasma_membrane
|
|
gptkbp:tissue_specificity
|
ubiquitous, highest in heart, muscle, kidney
|
|
gptkbp:transmembraneDomains
|
12
|
|
gptkbp:UniGene
|
Hs.65462
|
|
gptkbp:UniProtID
|
gptkb:Q9HC23
|
|
gptkbp:bfsParent
|
gptkb:PROK2
|
|
gptkbp:bfsLayer
|
8
|
|
http://www.w3.org/2000/01/rdf-schema#label
|
Q9HC23
|