Gene: ATP1A4
Ensembl ID : ENSG00000132681
Description: ATPase Na+/K+ transporting subunit alpha 4
Gene Synonyms: ATP1AL2
6 APIs:
571 Possible Orthologues:

Infectious disease R-HSA-5663205
Ion homeostasis R-HSA-5578775
SARS-CoV Infections R-HSA-9679506
Cardiac conduction R-HSA-5576891
Ion channel transport R-HSA-983712
Potential therapeutics for SARS R-HSA-9679191
Disease R-HSA-1643685
Muscle contraction R-HSA-397014
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551
Infectious disease R-HSA-5663205
Muscle contraction R-HSA-397014
Potential therapeutics for SARS R-HSA-9679191
Cardiac conduction R-HSA-5576891
Ion transport by P-type ATPases R-HSA-936837
Disease R-HSA-1643685
Transport of small molecules R-HSA-382551
SARS-CoV Infections R-HSA-9679506
Ion homeostasis R-HSA-5578775
Ion channel transport R-HSA-983712
Potential therapeutics for SARS R-HSA-9679191
Cardiac conduction R-HSA-5576891
Ion homeostasis R-HSA-5578775
Muscle contraction R-HSA-397014
Disease R-HSA-1643685
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
SARS-CoV Infections R-HSA-9679506
Infectious disease R-HSA-5663205
Ion transport by P-type ATPases R-HSA-936837
Ion homeostasis R-HSA-5578775
Infectious disease R-HSA-5663205
SARS-CoV Infections R-HSA-9679506
Potential therapeutics for SARS R-HSA-9679191
Ion transport by P-type ATPases R-HSA-936837
Disease R-HSA-1643685
Cardiac conduction R-HSA-5576891
Ion channel transport R-HSA-983712
Muscle contraction R-HSA-397014
Transport of small molecules R-HSA-382551
Ion transport by P-type ATPases R-HSA-936837
Disease R-HSA-1643685
Ion homeostasis R-HSA-5578775
Potential therapeutics for SARS R-HSA-9679191
Cardiac conduction R-HSA-5576891
Ion channel transport R-HSA-983712
Infectious disease R-HSA-5663205
Muscle contraction R-HSA-397014
SARS-CoV Infections R-HSA-9679506
Transport of small molecules R-HSA-382551
SARS-CoV Infections R-HSA-9679506
Potential therapeutics for SARS R-HSA-9679191
Transport of small molecules R-HSA-382551
Cardiac conduction R-HSA-5576891
Ion transport by P-type ATPases R-HSA-936837
Ion homeostasis R-HSA-5578775
Muscle contraction R-HSA-397014
Disease R-HSA-1643685
Infectious disease R-HSA-5663205
Ion channel transport R-HSA-983712
Infectious disease R-HSA-5663205
Potential therapeutics for SARS R-HSA-9679191
Disease R-HSA-1643685
Ion transport by P-type ATPases R-HSA-936837
SARS-CoV Infections R-HSA-9679506
Ion homeostasis R-HSA-5578775
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
Muscle contraction R-HSA-397014
Cardiac conduction R-HSA-5576891

Expression Atlas ENSG00000132681
NCBI gene (formerly Entrezgene) 480
GeneCards 14073
HGNC Symbol HGNC:14073
MIM gene 607321
UniProtKB Gene Name Q13733
WikiGene 480
Gene: SLC22A6
Ensembl ID : ENSG00000197901
Description: solute carrier family 22 member 6
Gene Synonyms: OAT1,PAHT,ROAT1
2 APIs:
495 Possible Orthologues:

Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Organic anion transport R-HSA-561048
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Organic cation/anion/zwitterion transport R-HSA-549132
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Organic cation/anion/zwitterion transport R-HSA-549132
SLC-mediated transmembrane transport R-HSA-425407
Organic anion transport R-HSA-561048
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Organic anion transport R-HSA-561048
Organic cation/anion/zwitterion transport R-HSA-549132
Transport of small molecules R-HSA-382551
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Organic cation/anion/zwitterion transport R-HSA-549132
Organic anion transport R-HSA-561048
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Organic anion transport R-HSA-561048
SLC-mediated transmembrane transport R-HSA-425407
Transport of small molecules R-HSA-382551
Organic cation/anion/zwitterion transport R-HSA-549132
Organic anion transport R-HSA-561048
Organic cation/anion/zwitterion transport R-HSA-549132
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Organic cation/anion/zwitterion transport R-HSA-549132
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Organic anion transport R-HSA-561048
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC-mediated transmembrane transport R-HSA-425407
Organic anion transport R-HSA-561048
Transport of small molecules R-HSA-382551
Organic cation/anion/zwitterion transport R-HSA-549132

Expression Atlas ENSG00000197901
NCBI gene (formerly Entrezgene) 9356
GeneCards 10970
HGNC Symbol HGNC:10970
MIM gene 607582
UniProtKB Gene Name Q4U2R8
WikiGene 9356
Gene: ATP1B2
Ensembl ID : ENSG00000129244
Description: ATPase Na+/K+ transporting subunit beta 2
Gene Synonyms: AMOG
6 APIs:
269 Possible Orthologues:

Muscle contraction R-HSA-397014
SARS-CoV Infections R-HSA-9679506
Potential therapeutics for SARS R-HSA-9679191
Transport of small molecules R-HSA-382551
Basigin interactions R-HSA-210991
Infectious disease R-HSA-5663205
Ion homeostasis R-HSA-5578775
Hemostasis R-HSA-109582
Cell surface interactions at the vascular wall R-HSA-202733
Disease R-HSA-1643685
Cardiac conduction R-HSA-5576891
Ion transport by P-type ATPases R-HSA-936837
Ion channel transport R-HSA-983712
SARS-CoV Infections R-HSA-9679506
Ion channel transport R-HSA-983712
Basigin interactions R-HSA-210991
Disease R-HSA-1643685
Hemostasis R-HSA-109582
Potential therapeutics for SARS R-HSA-9679191
Ion transport by P-type ATPases R-HSA-936837
Muscle contraction R-HSA-397014
Ion homeostasis R-HSA-5578775
Cardiac conduction R-HSA-5576891
Transport of small molecules R-HSA-382551
Infectious disease R-HSA-5663205
Cell surface interactions at the vascular wall R-HSA-202733
Disease R-HSA-1643685
Hemostasis R-HSA-109582
Ion channel transport R-HSA-983712
Basigin interactions R-HSA-210991
SARS-CoV Infections R-HSA-9679506
Infectious disease R-HSA-5663205
Ion transport by P-type ATPases R-HSA-936837
Ion homeostasis R-HSA-5578775
Cardiac conduction R-HSA-5576891
Potential therapeutics for SARS R-HSA-9679191
Transport of small molecules R-HSA-382551
Muscle contraction R-HSA-397014
Cell surface interactions at the vascular wall R-HSA-202733
Muscle contraction R-HSA-397014
Disease R-HSA-1643685
Infectious disease R-HSA-5663205
SARS-CoV Infections R-HSA-9679506
Potential therapeutics for SARS R-HSA-9679191
Transport of small molecules R-HSA-382551
Basigin interactions R-HSA-210991
Ion channel transport R-HSA-983712
Ion homeostasis R-HSA-5578775
Hemostasis R-HSA-109582
Ion transport by P-type ATPases R-HSA-936837
Cell surface interactions at the vascular wall R-HSA-202733
Cardiac conduction R-HSA-5576891
Ion transport by P-type ATPases R-HSA-936837
Hemostasis R-HSA-109582
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
Cell surface interactions at the vascular wall R-HSA-202733
Basigin interactions R-HSA-210991
Cardiac conduction R-HSA-5576891
SARS-CoV Infections R-HSA-9679506
Disease R-HSA-1643685
Ion homeostasis R-HSA-5578775
Potential therapeutics for SARS R-HSA-9679191
Muscle contraction R-HSA-397014
Infectious disease R-HSA-5663205
Basigin interactions R-HSA-210991
Transport of small molecules R-HSA-382551
Ion channel transport R-HSA-983712
Ion homeostasis R-HSA-5578775
Muscle contraction R-HSA-397014
Potential therapeutics for SARS R-HSA-9679191
Infectious disease R-HSA-5663205
Disease R-HSA-1643685
Hemostasis R-HSA-109582
SARS-CoV Infections R-HSA-9679506
Cardiac conduction R-HSA-5576891
Cell surface interactions at the vascular wall R-HSA-202733
Ion transport by P-type ATPases R-HSA-936837
Hemostasis R-HSA-109582
Disease R-HSA-1643685
Muscle contraction R-HSA-397014
Basigin interactions R-HSA-210991
Potential therapeutics for SARS R-HSA-9679191
Transport of small molecules R-HSA-382551
Cell surface interactions at the vascular wall R-HSA-202733
Ion transport by P-type ATPases R-HSA-936837
Ion homeostasis R-HSA-5578775
Infectious disease R-HSA-5663205
Ion channel transport R-HSA-983712
Cardiac conduction R-HSA-5576891
SARS-CoV Infections R-HSA-9679506
Ion transport by P-type ATPases R-HSA-936837
Infectious disease R-HSA-5663205
Transport of small molecules R-HSA-382551
Cell surface interactions at the vascular wall R-HSA-202733
Disease R-HSA-1643685
Potential therapeutics for SARS R-HSA-9679191
Ion channel transport R-HSA-983712
Cardiac conduction R-HSA-5576891
Ion homeostasis R-HSA-5578775
SARS-CoV Infections R-HSA-9679506
Basigin interactions R-HSA-210991
Muscle contraction R-HSA-397014
Hemostasis R-HSA-109582
Disease R-HSA-1643685
Muscle contraction R-HSA-397014
Hemostasis R-HSA-109582
Cell surface interactions at the vascular wall R-HSA-202733
SARS-CoV Infections R-HSA-9679506
Ion channel transport R-HSA-983712
Ion homeostasis R-HSA-5578775
Ion transport by P-type ATPases R-HSA-936837
Infectious disease R-HSA-5663205
Potential therapeutics for SARS R-HSA-9679191
Basigin interactions R-HSA-210991
Transport of small molecules R-HSA-382551
Cardiac conduction R-HSA-5576891
Disease R-HSA-1643685
Muscle contraction R-HSA-397014
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551
Infectious disease R-HSA-5663205
Ion channel transport R-HSA-983712
Ion homeostasis R-HSA-5578775
Potential therapeutics for SARS R-HSA-9679191
Hemostasis R-HSA-109582
Cell surface interactions at the vascular wall R-HSA-202733
Basigin interactions R-HSA-210991
SARS-CoV Infections R-HSA-9679506
Cardiac conduction R-HSA-5576891

Expression Atlas ENSG00000129244
NCBI gene (formerly Entrezgene) 482
GeneCards 805
HGNC Symbol HGNC:805
MIM gene 182331
UniProtKB Gene Name P14415
WikiGene 482
Gene: SLC6A2
Ensembl ID : ENSG00000103546
Description: solute carrier family 6 member 2
Gene Synonyms: NAT1,NET,NET1,SLC6A5
63 APIs:
204 Possible Orthologues:

Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Disease R-HSA-1643685
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
SLC transporter disorders R-HSA-5619102
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Disorders of transmembrane transporters R-HSA-5619115
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of small molecules R-HSA-382551
Disease R-HSA-1643685
SLC transporter disorders R-HSA-5619102
SLC-mediated transmembrane transport R-HSA-425407
Disorders of transmembrane transporters R-HSA-5619115
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Disorders of transmembrane transporters R-HSA-5619115
SLC-mediated transmembrane transport R-HSA-425407
Disease R-HSA-1643685
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
SLC transporter disorders R-HSA-5619102
SLC-mediated transmembrane transport R-HSA-425407
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Disease R-HSA-1643685
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
SLC transporter disorders R-HSA-5619102
Disorders of transmembrane transporters R-HSA-5619115
Disease R-HSA-1643685
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
SLC transporter disorders R-HSA-5619102
Disorders of transmembrane transporters R-HSA-5619115
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Disease R-HSA-1643685
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of small molecules R-HSA-382551
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC transporter disorders R-HSA-5619102
SLC-mediated transmembrane transport R-HSA-425407
Disorders of transmembrane transporters R-HSA-5619115
SLC-mediated transmembrane transport R-HSA-425407
Disorders of transmembrane transporters R-HSA-5619115
Disease R-HSA-1643685
Transport of small molecules R-HSA-382551
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
SLC transporter disorders R-HSA-5619102
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
Transport of small molecules R-HSA-382551
Disorders of transmembrane transporters R-HSA-5619115
SLC-mediated transmembrane transport R-HSA-425407
Disease R-HSA-1643685
SLC transporter disorders R-HSA-5619102
SLC transporter disorders R-HSA-5619102
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Disorders of transmembrane transporters R-HSA-5619115
SLC-mediated transmembrane transport R-HSA-425407
Transport of small molecules R-HSA-382551
Disease R-HSA-1643685
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Defective SLC6A2 causes orthostatic intolerance (OI) R-HSA-5619109
SLC transporter disorders R-HSA-5619102
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Disorders of transmembrane transporters R-HSA-5619115
SLC-mediated transmembrane transport R-HSA-425407
Disease R-HSA-1643685
Transport of small molecules R-HSA-382551

Expression Atlas ENSG00000103546
NCBI gene (formerly Entrezgene) 6530
GeneCards 11048
HGNC Symbol HGNC:11048
MIM gene 163970
MIM morbid 604715
UniProtKB Gene Name P23975
WikiGene 6530
Gene: ATP4B
Ensembl ID : ENSG00000186009
Description: ATPase H+/K+ transporting subunit beta
Gene Synonyms: ATP6B
12 APIs:
171 Possible Orthologues:

Ion channel transport R-HSA-983712
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551
Ion transport by P-type ATPases R-HSA-936837
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
Ion transport by P-type ATPases R-HSA-936837
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
Transport of small molecules R-HSA-382551
Ion channel transport R-HSA-983712
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551
Ion transport by P-type ATPases R-HSA-936837
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
Ion transport by P-type ATPases R-HSA-936837
Ion channel transport R-HSA-983712
Ion channel transport R-HSA-983712
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551
Ion channel transport R-HSA-983712
Transport of small molecules R-HSA-382551
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551
Ion channel transport R-HSA-983712
Ion transport by P-type ATPases R-HSA-936837
Ion channel transport R-HSA-983712
Ion transport by P-type ATPases R-HSA-936837
Transport of small molecules R-HSA-382551

Expression Atlas ENSG00000186009
NCBI gene (formerly Entrezgene) 496
GeneCards 820
HGNC Symbol HGNC:820
MIM gene 137217
UniProtKB Gene Name P51164
WikiGene 496
Gene: KCNJ11
Ensembl ID : ENSG00000187486
Description: potassium inwardly rectifying channel subfamily J member 11
Gene Synonyms: BIR,KIR6.2
13 APIs:
190 Possible Orthologues:

ATP sensitive Potassium channels R-HSA-1296025
Ion homeostasis R-HSA-5578775
Neuronal System R-HSA-112316
Cardiac conduction R-HSA-5576891
Metabolism R-HSA-1430728
Ion homeostasis R-HSA-5578775
Integration of energy metabolism R-HSA-163685
Regulation of insulin secretion R-HSA-422356
Muscle contraction R-HSA-397014
Inwardly rectifying K+ channels R-HSA-1296065
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Transport of small molecules R-HSA-382551
ABC-family proteins mediated transport R-HSA-382556
ABC transporter disorders R-HSA-5619084
Potassium Channels R-HSA-1296071
ATP sensitive Potassium channels R-HSA-1296025
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Disorders of transmembrane transporters R-HSA-5619115
Disease R-HSA-1643685
Regulation of insulin secretion R-HSA-422356
Transport of small molecules R-HSA-382551
Metabolism R-HSA-1430728
Inwardly rectifying K+ channels R-HSA-1296065
Neuronal System R-HSA-112316
ABC transporter disorders R-HSA-5619084
Disease R-HSA-1643685
ABC-family proteins mediated transport R-HSA-382556
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Integration of energy metabolism R-HSA-163685
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Muscle contraction R-HSA-397014
Cardiac conduction R-HSA-5576891
Disorders of transmembrane transporters R-HSA-5619115
Potassium Channels R-HSA-1296071
Cardiac conduction R-HSA-5576891
Transport of small molecules R-HSA-382551
Potassium Channels R-HSA-1296071
Neuronal System R-HSA-112316
Ion homeostasis R-HSA-5578775
ABC-family proteins mediated transport R-HSA-382556
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Disorders of transmembrane transporters R-HSA-5619115
Integration of energy metabolism R-HSA-163685
Metabolism R-HSA-1430728
Disease R-HSA-1643685
Muscle contraction R-HSA-397014
ATP sensitive Potassium channels R-HSA-1296025
Regulation of insulin secretion R-HSA-422356
Inwardly rectifying K+ channels R-HSA-1296065
ABC transporter disorders R-HSA-5619084
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Ion homeostasis R-HSA-5578775
Inwardly rectifying K+ channels R-HSA-1296065
ABC-family proteins mediated transport R-HSA-382556
Potassium Channels R-HSA-1296071
Integration of energy metabolism R-HSA-163685
Regulation of insulin secretion R-HSA-422356
Muscle contraction R-HSA-397014
Metabolism R-HSA-1430728
Disorders of transmembrane transporters R-HSA-5619115
ABC transporter disorders R-HSA-5619084
Transport of small molecules R-HSA-382551
Disease R-HSA-1643685
Cardiac conduction R-HSA-5576891
ATP sensitive Potassium channels R-HSA-1296025
Neuronal System R-HSA-112316
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
ATP sensitive Potassium channels R-HSA-1296025
Disease R-HSA-1643685
ABC transporter disorders R-HSA-5619084
Potassium Channels R-HSA-1296071
Metabolism R-HSA-1430728
Inwardly rectifying K+ channels R-HSA-1296065
Neuronal System R-HSA-112316
Integration of energy metabolism R-HSA-163685
Cardiac conduction R-HSA-5576891
Ion homeostasis R-HSA-5578775
Regulation of insulin secretion R-HSA-422356
Transport of small molecules R-HSA-382551
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Muscle contraction R-HSA-397014
ABC-family proteins mediated transport R-HSA-382556
Disorders of transmembrane transporters R-HSA-5619115
ABC transporter disorders R-HSA-5619084
ABC-family proteins mediated transport R-HSA-382556
Integration of energy metabolism R-HSA-163685
Cardiac conduction R-HSA-5576891
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Ion homeostasis R-HSA-5578775
Regulation of insulin secretion R-HSA-422356
ATP sensitive Potassium channels R-HSA-1296025
Disorders of transmembrane transporters R-HSA-5619115
Neuronal System R-HSA-112316
Muscle contraction R-HSA-397014
Potassium Channels R-HSA-1296071
Transport of small molecules R-HSA-382551
Inwardly rectifying K+ channels R-HSA-1296065
Metabolism R-HSA-1430728
Disease R-HSA-1643685
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Neuronal System R-HSA-112316
Disorders of transmembrane transporters R-HSA-5619115
ATP sensitive Potassium channels R-HSA-1296025
Inwardly rectifying K+ channels R-HSA-1296065
ABC transporter disorders R-HSA-5619084
Muscle contraction R-HSA-397014
Potassium Channels R-HSA-1296071
Metabolism R-HSA-1430728
ABC-family proteins mediated transport R-HSA-382556
Cardiac conduction R-HSA-5576891
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Ion homeostasis R-HSA-5578775
Transport of small molecules R-HSA-382551
Disease R-HSA-1643685
Regulation of insulin secretion R-HSA-422356
Integration of energy metabolism R-HSA-163685
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Regulation of insulin secretion R-HSA-422356
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Ion homeostasis R-HSA-5578775
Disease R-HSA-1643685
Potassium Channels R-HSA-1296071
Metabolism R-HSA-1430728
Transport of small molecules R-HSA-382551
Muscle contraction R-HSA-397014
ABC transporter disorders R-HSA-5619084
Neuronal System R-HSA-112316
Inwardly rectifying K+ channels R-HSA-1296065
ABC-family proteins mediated transport R-HSA-382556
Integration of energy metabolism R-HSA-163685
ATP sensitive Potassium channels R-HSA-1296025
Disorders of transmembrane transporters R-HSA-5619115
Cardiac conduction R-HSA-5576891
Potassium Channels R-HSA-1296071
Transport of small molecules R-HSA-382551
Neuronal System R-HSA-112316
Inwardly rectifying K+ channels R-HSA-1296065
Metabolism R-HSA-1430728
ABC transporter disorders R-HSA-5619084
Ion homeostasis R-HSA-5578775
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
ATP sensitive Potassium channels R-HSA-1296025
Cardiac conduction R-HSA-5576891
Integration of energy metabolism R-HSA-163685
Muscle contraction R-HSA-397014
Disorders of transmembrane transporters R-HSA-5619115
ABC-family proteins mediated transport R-HSA-382556
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Disease R-HSA-1643685
Regulation of insulin secretion R-HSA-422356
Metabolism R-HSA-1430728
Transport of small molecules R-HSA-382551
ABC-family proteins mediated transport R-HSA-382556
Potassium Channels R-HSA-1296071
Ion homeostasis R-HSA-5578775
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
Integration of energy metabolism R-HSA-163685
ATP sensitive Potassium channels R-HSA-1296025
Cardiac conduction R-HSA-5576891
Disorders of transmembrane transporters R-HSA-5619115
Muscle contraction R-HSA-397014
Disease R-HSA-1643685
Neuronal System R-HSA-112316
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
ABC transporter disorders R-HSA-5619084
Inwardly rectifying K+ channels R-HSA-1296065
Regulation of insulin secretion R-HSA-422356
Disorders of transmembrane transporters R-HSA-5619115
Muscle contraction R-HSA-397014
Defective ABCC9 causes CMD10, ATFB12 and Cantu syndrome R-HSA-5678420
ABC transporter disorders R-HSA-5619084
Disease R-HSA-1643685
Defective ABCC8 can cause hypo- and hyper-glycemias R-HSA-5683177
Metabolism R-HSA-1430728
Potassium Channels R-HSA-1296071
ABC-family proteins mediated transport R-HSA-382556
ATP sensitive Potassium channels R-HSA-1296025
Ion homeostasis R-HSA-5578775
Neuronal System R-HSA-112316
Integration of energy metabolism R-HSA-163685
Inwardly rectifying K+ channels R-HSA-1296065
Regulation of insulin secretion R-HSA-422356
Cardiac conduction R-HSA-5576891
Transport of small molecules R-HSA-382551

Expression Atlas ENSG00000187486
NCBI gene (formerly Entrezgene) 3767
GeneCards 6257
HGNC Symbol HGNC:6257
MIM gene 600937
MIM morbid 618856
UniProtKB Gene Name Q14654
WikiGene 3767
Gene: SLC6A3
Ensembl ID : ENSG00000142319
Description: solute carrier family 6 member 3
Gene Synonyms: DAT,DAT1
21 APIs:
167 Possible Orthologues:

Disease R-HSA-1643685
SLC transporter disorders R-HSA-5619102
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Neurotransmitter clearance R-HSA-112311
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Neuronal System R-HSA-112316
Disorders of transmembrane transporters R-HSA-5619115
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Dopamine clearance from the synaptic cleft R-HSA-379401
Transmission across Chemical Synapses R-HSA-112315
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Disease R-HSA-1643685
Neurotransmitter clearance R-HSA-112311
SLC-mediated transmembrane transport R-HSA-425407
Transport of small molecules R-HSA-382551
SLC transporter disorders R-HSA-5619102
Neuronal System R-HSA-112316
Disorders of transmembrane transporters R-HSA-5619115
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
Dopamine clearance from the synaptic cleft R-HSA-379401
Transmission across Chemical Synapses R-HSA-112315
Neurotransmitter clearance R-HSA-112311
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Neuronal System R-HSA-112316
SLC-mediated transmembrane transport R-HSA-425407
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Disorders of transmembrane transporters R-HSA-5619115
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
Disease R-HSA-1643685
Transmission across Chemical Synapses R-HSA-112315
Dopamine clearance from the synaptic cleft R-HSA-379401
Transport of small molecules R-HSA-382551
SLC transporter disorders R-HSA-5619102
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Neurotransmitter clearance R-HSA-112311
Transmission across Chemical Synapses R-HSA-112315
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC transporter disorders R-HSA-5619102
Disease R-HSA-1643685
Transport of small molecules R-HSA-382551
Neuronal System R-HSA-112316
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
SLC-mediated transmembrane transport R-HSA-425407
Dopamine clearance from the synaptic cleft R-HSA-379401
Disorders of transmembrane transporters R-HSA-5619115
SLC transporter disorders R-HSA-5619102
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Neurotransmitter clearance R-HSA-112311
Transport of small molecules R-HSA-382551
Transmission across Chemical Synapses R-HSA-112315
SLC-mediated transmembrane transport R-HSA-425407
Dopamine clearance from the synaptic cleft R-HSA-379401
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Neuronal System R-HSA-112316
Disorders of transmembrane transporters R-HSA-5619115
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
Disease R-HSA-1643685
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Disease R-HSA-1643685
Neurotransmitter clearance R-HSA-112311
Transport of small molecules R-HSA-382551
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
SLC transporter disorders R-HSA-5619102
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transmission across Chemical Synapses R-HSA-112315
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Neuronal System R-HSA-112316
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Dopamine clearance from the synaptic cleft R-HSA-379401
Disorders of transmembrane transporters R-HSA-5619115
SLC-mediated transmembrane transport R-HSA-425407
Disease R-HSA-1643685
Dopamine clearance from the synaptic cleft R-HSA-379401
Transmission across Chemical Synapses R-HSA-112315
Neuronal System R-HSA-112316
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Neurotransmitter clearance R-HSA-112311
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
SLC-mediated transmembrane transport R-HSA-425407
SLC transporter disorders R-HSA-5619102
Transport of small molecules R-HSA-382551
Disorders of transmembrane transporters R-HSA-5619115
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
SLC transporter disorders R-HSA-5619102
Neurotransmitter clearance R-HSA-112311
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC-mediated transmembrane transport R-HSA-425407
Disorders of transmembrane transporters R-HSA-5619115
Dopamine clearance from the synaptic cleft R-HSA-379401
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of small molecules R-HSA-382551
Neuronal System R-HSA-112316
Disease R-HSA-1643685
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Transmission across Chemical Synapses R-HSA-112315
Disease R-HSA-1643685
Transport of small molecules R-HSA-382551
Dopamine clearance from the synaptic cleft R-HSA-379401
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transmission across Chemical Synapses R-HSA-112315
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5660724
Neuronal System R-HSA-112316
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC-mediated transmembrane transport R-HSA-425407
Neurotransmitter clearance R-HSA-112311
SLC transporter disorders R-HSA-5619102
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS) R-HSA-5619081
Disorders of transmembrane transporters R-HSA-5619115

Expression Atlas ENSG00000142319
NCBI gene (formerly Entrezgene) 6531
GeneCards 11049
HGNC Symbol HGNC:11049
MIM gene 126455
MIM morbid 613135
UniProtKB Gene Name Q01959
WikiGene 6531
Gene: SLC6A9
Ensembl ID : ENSG00000196517
Description: solute carrier family 6 member 9
Gene Synonyms: GLYT-1,GLYT1
3 APIs:
207 Possible Orthologues:

Transport of small molecules R-HSA-382551
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
SLC-mediated transmembrane transport R-HSA-425407
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
SLC-mediated transmembrane transport R-HSA-425407
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC-mediated transmembrane transport R-HSA-425407
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of small molecules R-HSA-382551
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
SLC-mediated transmembrane transport R-HSA-425407
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
SLC-mediated transmembrane transport R-HSA-425407
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC-mediated transmembrane transport R-HSA-425407
Transport of small molecules R-HSA-382551
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Transport of small molecules R-HSA-382551
SLC-mediated transmembrane transport R-HSA-425407
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660
Transport of small molecules R-HSA-382551
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
SLC-mediated transmembrane transport R-HSA-425407
SLC-mediated transmembrane transport R-HSA-425407
Transport of small molecules R-HSA-382551
Transport of bile salts and organic acids, metal ions and amine compounds R-HSA-425366
Na+/Cl- dependent neurotransmitter transporters R-HSA-442660

Expression Atlas ENSG00000196517
NCBI gene (formerly Entrezgene) 6536
GeneCards 11056
HGNC Symbol HGNC:11056
MIM gene 601019
MIM morbid 617301
UniProtKB Gene Name P48067
WikiGene 6536