Name

CORUM Protein Complexes Dataset

From CORUM

proteins participating in complexes by manual literature curation

NURSA Protein Complexes Dataset

From Nuclear Receptor Signaling Atlas

proteins identified in complexes isolated from cultured cells

ATP5C1 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the gamma subunit of the catalytic core. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene also has a pseudogene on chromosome 14. [provided by RefSeq, Jul 2008]

ATP5L2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit G2

LOC100127892 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene

LOC100289091 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit G2 pseudogene

ATP5BP1 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide pseudogene 1

ATP5J2LP Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2-like pseudogene

LOC100288416 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene

LOC101928296 Gene

ATP synthase-coupling factor 6, mitochondrial-like

ATP5JP1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6 pseudogene 1

ATP5A1 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1, cardiac muscle

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, using an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the alpha subunit of the catalytic core. Alternatively spliced transcript variants encoding the different isoforms have been identified. Pseudogenes of this gene are located on chromosomes 9, 2, and 16. [provided by RefSeq, Mar 2012]

ATP5J2P6 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 6

ATP5J2P4 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 4

ATP5J2P5 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 5

ATP5J2P2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 2

ATP5J2P3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2 pseudogene 3

ATP5S Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit s (factor B)

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. This gene encodes the subunit s, also known as factor B, of the proton channel. This subunit is necessary for the energy transduction activity of the ATP synthase complexes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

ATP5J Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F6

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the F6 subunit of the Fo complex, required for F1 and Fo interactions. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. A pseudogene exists on chromosome Yp11.[provided by RefSeq, Jun 2010]

ATP5I Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit E

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the e subunit of the Fo complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010]

ATP5H Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the d subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. In addition, three pseudogenes are located on chromosomes 9, 12 and 15. [provided by RefSeq, Jun 2010]

ATP5O Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit

The protein encoded by this gene is a component of the F-type ATPase found in the mitochondrial matrix. F-type ATPases are composed of a catalytic core and a membrane proton channel. The encoded protein appears to be part of the connector linking these two components and may be involved in transmission of conformational changes or proton conductance. [provided by RefSeq, Jul 2008]

ATP5B Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the beta subunit of the catalytic core. [provided by RefSeq, Jul 2008]

ATP5E Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the epsilon subunit of the catalytic core. Two pseudogenes of this gene are located on chromosomes 4 and 13. Read-through transcripts that include exons from this gene are expressed from the upstream gene SLMO2.[provided by RefSeq, Mar 2011]

ATP5D Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel consists of three main subunits (a, b, c). This gene encodes the delta subunit of the catalytic core. Alternatively spliced transcript variants encoding the same isoform have been identified. [provided by RefSeq, Jul 2008]

LIG4 Gene

ligase IV, DNA, ATP-dependent

The protein encoded by this gene is a DNA ligase that joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ). This protein forms a complex with the X-ray repair cross complementing protein 4 (XRCC4), and further interacts with the DNA-dependent protein kinase (DNA-PK). Both XRCC4 and DNA-PK are known to be required for NHEJ. The crystal structure of the complex formed by this protein and XRCC4 has been resolved. Defects in this gene are the cause of LIG4 syndrome. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008]

LIG1 Gene

ligase I, DNA, ATP-dependent

This gene encodes a member of the ATP-dependent DNA ligase protein family. The encoded protein functions in DNA replication, recombination, and the base excision repair process. Mutations in this gene that lead to DNA ligase I deficiency result in immunodeficiency and increased sensitivity to DNA-damaging agents. Disruption of this gene may also be associated with a variety of cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

LIG3 Gene

ligase III, DNA, ATP-dependent

This gene is a member of the DNA ligase family. Each member of this family encodes a protein that catalyzes the joining of DNA ends but they each have a distinct role in DNA metabolism. The protein encoded by this gene is involved in excision repair and is located in both the mitochondria and nucleus, with translation initiation from the upstream start codon allowing for transport to the mitochondria and translation initiation from a downstream start codon allowing for transport to the nucleus. Additionally, alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

LOC100132849 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit pseudogene

ACLY Gene

ATP citrate lyase

ATP citrate lyase is the primary enzyme responsible for the synthesis of cytosolic acetyl-CoA in many tissues. The enzyme is a tetramer (relative molecular weight approximately 440,000) of apparently identical subunits. It catalyzes the formation of acetyl-CoA and oxaloacetate from citrate and CoA with a concomitant hydrolysis of ATP to ADP and phosphate. The product, acetyl-CoA, serves several important biosynthetic pathways, including lipogenesis and cholesterogenesis. In nervous tissue, ATP citrate-lyase may be involved in the biosynthesis of acetylcholine. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Dec 2014]

ATP5C1P1 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 pseudogene 1

LOC100507083 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene

ATP5J2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The catalytic portion of mitochondrial ATP synthase consists of five different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the f subunit of the Fo complex. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. This gene has multiple pseudogenes. Naturally occurring read-through transcription also exists between this gene and the downstream pentatricopeptide repeat domain 1 (PTCD1) gene. [provided by RefSeq, Nov 2010]

ATP5EP1 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 1

ATP5EP2 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, epsilon subunit pseudogene 2

LOC102725121 Gene

putative ATP-dependent RNA helicase DDX12

ATP5G2P1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 1

ATP5G2P3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 3

ATP5G2P2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 2

ATP5G2P4 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9) pseudogene 4

ATP5HP1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 1

ATP5HP3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 3

ATP5HP2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 2

ATP5HP4 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit d, pseudogene 4

HFM1 Gene

HFM1, ATP-dependent DNA helicase homolog (S. cerevisiae)

The protein encoded by this gene is thought to be an ATP-dependent DNA helicase and is expressed mainly in germ-line cells. Defects in this gene are a cause of premature ovarian failure 9 (POF9). [provided by RefSeq, Apr 2014]

ATP5G3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C3 (subunit 9)

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding different proteins have been identified. [provided by RefSeq, Jun 2010]

ATP5G2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C2 (subunit 9)

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and single representatives of the gamma, delta, and epsilon subunits. The proton channel likely has nine subunits (a, b, c, d, e, f, g, F6 and 8). There are three separate genes which encode subunit c of the proton channel and they specify precursors with different import sequences but identical mature proteins. The protein encoded by this gene is one of three precursors of subunit c. Alternatively spliced transcript variants encoding different isoforms have been identified. This gene has multiple pseudogenes. [provided by RefSeq, Jun 2010]

ATP5A1P4 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 4

ATP5A1P5 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 5

ATP5A1P7 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 7

ATP5A1P2 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 2

ATP5A1P3 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 3

ATP5A1P8 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 8

ATP5A1P10 Gene

ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit 1 pseudogene 10

ATP5F1P1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 1

ATP5F1P3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 3

ATP5F1P5 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 5

ATP5F1P4 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 4

ATP5F1P7 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 7

ATP5F1P6 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 6

MT-ATP8 Gene

ATP synthase F0 subunit 8

MT-ATP6 Gene

ATP synthase F0 subunit 6

ATPAF2 Gene

ATP synthase mitochondrial F1 complex assembly factor 2

This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 alpha subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. This gene is located within the Smith-Magenis syndrome region on chromosome 17. An alternatively spliced transcript variant has been described, but its biological validity has not been determined. [provided by RefSeq, Jul 2008]

ATPAF1 Gene

ATP synthase mitochondrial F1 complex assembly factor 1

This gene encodes an assembly factor for the F(1) component of the mitochondrial ATP synthase. This protein binds specifically to the F1 beta subunit and is thought to prevent this subunit from forming nonproductive homooligomers during enzyme assembly. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]

LOC100510709 Gene

ADP/ATP translocase 2-like

ATP5LP5 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 5

ATP5LP4 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 4

ATP5LP7 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 7

ATP5LP6 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 6

ATP5LP1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 1

ATP5LP3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 3

ATP5LP2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 2

ATP5LP8 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit g, pseudogene 8

ATP5G1P3 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 3

ATP5G1P1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 1

ATP5F1P2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1 pseudogene 2

HLCS Gene

holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)

This gene encodes an enzyme that catalyzes the binding of biotin to carboxylases and histones. The protein plays an important role in gluconeogenesis, fatty acid synthesis and branched chain amino acid catabolism. Defects in this gene are the cause of holocarboxylase synthetase deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jun 2011]

ATP5L Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit G

Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. It is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, which comprises the proton channel. The F1 complex consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled in a ratio of 3 alpha, 3 beta, and a single representative of the other 3. The Fo seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the g subunit of the Fo complex. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jun 2010]

ATP5G1P2 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 2

ATP5G1P6 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 6

ATP5G1P7 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 7

ATP5G1P4 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 4

ATP5G1P5 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 5

ATP5G1P8 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9) pseudogene 8

MTATP6P2 Gene

mitochondrially encoded ATP synthase 6 pseudogene 2

ATP5F1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit B1

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene encodes the b subunit of the proton channel. [provided by RefSeq, Jul 2008]

OPLAH Gene

5-oxoprolinase (ATP-hydrolysing)

The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]

LOC644303 Gene

ATP-dependent RNA helicase DDX24-like

LOC100287966 Gene

ATP synthase-coupling factor 6, mitochondrial-like

ATP5G1 Gene

ATP synthase, H+ transporting, mitochondrial Fo complex, subunit C1 (subunit 9)

This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. The catalytic portion of mitochondrial ATP synthase consists of 5 different subunits (alpha, beta, gamma, delta, and epsilon) assembled with a stoichiometry of 3 alpha, 3 beta, and a single representative of the other 3. The proton channel seems to have nine subunits (a, b, c, d, e, f, g, F6 and 8). This gene is one of three genes that encode subunit c of the proton channel. Each of the three genes have distinct mitochondrial import sequences but encode the identical mature protein. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]

MAGT1 Gene

magnesium transporter 1

This gene encodes a magnesium cation transporter protein that localizes to the cell membrane. This protein also associates with N-oligosaccharyl transferase and therefore may have a role in N-glycosylation. Mutations in this gene cause mental retardation X-linked type 95 (MRX95). This gene may have multiple in-frame translation initiation sites, one of which would encode a shorter protein with an N-terminus containing a signal peptide at amino acids 1-29. [provided by RefSeq, Jan 2010]

TAP1 Gene

transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. The protein encoded by this gene is involved in the pumping of degraded cytosolic peptides across the endoplasmic reticulum into the membrane-bound compartment where class I molecules assemble. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]

TAP2 Gene

transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance. This gene is located 7 kb telomeric to gene family member ABCB2. The protein encoded by this gene is involved in antigen presentation. This protein forms a heterodimer with ABCB2 in order to transport peptides from the cytoplasm to the endoplasmic reticulum. Mutations in this gene may be associated with ankylosing spondylitis, insulin-dependent diabetes mellitus, and celiac disease. Alternative splicing of this gene produces products which differ in peptide selectivity and level of restoration of surface expression of MHC class I molecules. [provided by RefSeq, Feb 2014]

SLC18A3 Gene

solute carrier family 18 (vesicular acetylcholine transporter), member 3

This gene is a member of the vesicular amine transporter family. The encoded transmembrane protein transports acetylcholine into secretory vesicles for release into the extracellular space. Acetylcholine transport utilizes a proton gradient established by a vacuolar ATPase. This gene is located within the first intron of the choline acetyltransferase gene. [provided by RefSeq, Jul 2008]

SLC18A2 Gene

solute carrier family 18 (vesicular monoamine transporter), member 2

The vesicular monoamine transporter acts to accumulate cytosolic monoamines into synaptic vesicles, using the proton gradient maintained across the synaptic vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (summary by Peter et al., 1993 [PubMed 7905859]). See also SLC18A1 (MIM 193002).[supplied by OMIM, Jan 2011]

SLC18A1 Gene

solute carrier family 18 (vesicular monoamine transporter), member 1

The vesicular monoamine transporter acts to accumulate cytosolic monoamines into vesicles, using the proton gradient maintained across the vesicular membrane. Its proper function is essential to the correct activity of the monoaminergic systems that have been implicated in several human neuropsychiatric disorders. The transporter is a site of action of important drugs, including reserpine and tetrabenazine (Peter et al., 1993 [PubMed 7905859]). See also SLC18A2 (MIM 193001).[supplied by OMIM, Mar 2008]

SLC17A9 Gene

solute carrier family 17 (vesicular nucleotide transporter), member 9

This gene encodes a member of a family of transmembrane proteins that are involved in the transport of small molecules. The encoded protein participates in the vesicular uptake, storage, and secretion of adenoside triphosphate (ATP) and other nucleotides. A mutation in this gene was found in individuals with autosomal dominant disseminated superficial actinic porokeratosis-8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2014]

SLC17A5 Gene

solute carrier family 17 (acidic sugar transporter), member 5

This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]

SLC17A6 Gene

solute carrier family 17 (vesicular glutamate transporter), member 6

SLC17A7 Gene

solute carrier family 17 (vesicular glutamate transporter), member 7

The protein encoded by this gene is a vesicle-bound, sodium-dependent phosphate transporter that is specifically expressed in the neuron-rich regions of the brain. It is preferentially associated with the membranes of synaptic vesicles and functions in glutamate transport. The protein shares 82% identity with the differentiation-associated Na-dependent inorganic phosphate cotransporter and they appear to form a distinct class within the Na+/Pi cotransporter family. [provided by RefSeq, Jul 2008]

SLC17A1 Gene

solute carrier family 17 (organic anion transporter), member 1

SLC17A3 Gene

solute carrier family 17 (organic anion transporter), member 3

The protein encoded by this gene is a voltage-driven transporter that excretes intracellular urate and organic anions from the blood into renal tubule cells. Two transcript variants encoding different isoforms have been found for this gene. The longer isoform is a plasma membrane protein with transporter activity while the shorter isoform localizes to the endoplasmic reticulum. [provided by RefSeq, Aug 2012]

SLC22A2 Gene

solute carrier family 22 (organic cation transporter), member 2

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. It is found primarily in the kidney, where it may mediate the first step in cation reabsorption. [provided by RefSeq, Jul 2008]

SLC7A6 Gene

solute carrier family 7 (amino acid transporter light chain, y+L system), member 6

SLC7A1 Gene

solute carrier family 7 (cationic amino acid transporter, y+ system), member 1

SLC25A37 Gene

solute carrier family 25 (mitochondrial iron transporter), member 37

SLC25A37 is a solute carrier localized in the mitochondrial inner membrane. It functions as an essential iron importer for the synthesis of mitochondrial heme and iron-sulfur clusters (summary by Chen et al., 2009 [PubMed 19805291]).[supplied by OMIM, Jan 2011]

OCTN3 Gene

organic cation transporter 3

SLC6A20 Gene

solute carrier family 6 (proline IMINO transporter), member 20

Transport of small hydrophilic substances across cell membranes is mediated by substrate-specific transporter proteins which have been classified into several families of related genes. The protein encoded by this gene is a member of the subgroup of transporter with unidentified substrates within the Na+ and Cl- coupled transporter family. This gene is expressed in kidney, and its alternative splicing generates 2 transcript variants. [provided by RefSeq, Jul 2008]

LOC100130121 Gene

solute carrier family 19 (thiamine transporter), member 3 pseudogene

SLC23A2 Gene

solute carrier family 23 (ascorbic acid transporter), member 2

The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two required transporters and the encoded protein accounts for tissue-specific uptake of vitamin C. Previously, this gene had an official symbol of SLC23A1. [provided by RefSeq, Jul 2008]

SLC17A8 Gene

solute carrier family 17 (vesicular glutamate transporter), member 8

This gene encodes a vesicular glutamate transporter. The encoded protein transports the neurotransmitter glutamate into synaptic vesicles before it is released into the synaptic cleft. Mutations in this gene are the cause of autosomal-dominant nonsyndromic type 25 deafness. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

SLC37A1 Gene

solute carrier family 37 (glucose-6-phosphate transporter), member 1

SLC37A1, a member of the sugar-phosphate transport family, transports glycerol-3-phosphate (G3P) between cellular compartments for its utilization in several compartment-specific biochemical pathways.[supplied by OMIM, Jul 2004]

LOC100287294 Gene

equilibrative nucleoside transporter 4-like

SLCO2B1 Gene

solute carrier organic anion transporter family, member 2B1

This locus encodes a member of the organic anion-transporting polypeptide family of membrane proteins. The protein encoded by this locus may function in regulation of placental uptake of sulfated steroids. Alternatively spliced transcript variants have been described. [provided by RefSeq, Nov 2010]

SLCO1A2 Gene

solute carrier organic anion transporter family, member 1A2

This gene encodes a sodium-independent transporter which mediates cellular uptake of organic ions in the liver. Its substrates include bile acids, bromosulphophthalein, and some steroidal compounds. The protein is a member of the SLC21A family of solute carriers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2008]

SLC31A1 Gene

solute carrier family 31 (copper transporter), member 1

The protein encoded by this gene is a high-affinity copper transporter found in the cell membrane. The encoded protein functions as a homotrimer to effect the uptake of dietary copper. [provided by RefSeq, Aug 2011]

SLC31A2 Gene

solute carrier family 31 (copper transporter), member 2

SLC31A1P1 Gene

solute carrier family 31 (copper transporter), member 1 pseudogene 1

SLC35C2 Gene

solute carrier family 35 (GDP-fucose transporter), member C2

This gene encodes a member of the triose-phosphate transporter protein family. This gene is regulated by oxygen tension, is induced in hypoxic trophoblast cells, and is overexpressed in ovarian cancer. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been defined on the X chromosome. [provided by RefSeq, Jul 2013]

SLC35C1 Gene

solute carrier family 35 (GDP-fucose transporter), member C1

This gene encodes a GDP-fucose transporter that is found in the Golgi apparatus. Mutations in this gene result in congenital disorder of glycosylation type IIc. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2009]

LOC100422091 Gene

solute carrier family 30 (zinc transporter), member 6 pseudogene

SLC29A4 Gene

solute carrier family 29 (equilibrative nucleoside transporter), member 4

This gene encodes a member of the SLC29A/ENT transporter protein family. The encoded membrane protein catalyzes the reuptake of monoamines into presynaptic neurons, thus determining the intensity and duration of monoamine neural signaling. It has been shown to transport several compounds, including serotonin, dopamine, and the neurotoxin 1-methyl-4-phenylpyridinium. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

SLC29A3 Gene

solute carrier family 29 (equilibrative nucleoside transporter), member 3

This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010]

SLC29A2 Gene

solute carrier family 29 (equilibrative nucleoside transporter), member 2

The uptake of nucleosides by transporters, such as SLC29A2, is essential for nucleotide synthesis by salvage pathways in cells that lack de novo biosynthetic pathways. Nucleoside transport also plays a key role in the regulation of many physiologic processes through its effect on adenosine concentration at the cell surface (Griffiths et al., 1997 [PubMed 9396714]).[supplied by OMIM, Nov 2008]

SLC29A1 Gene

solute carrier family 29 (equilibrative nucleoside transporter), member 1

This gene is a member of the equilibrative nucleoside transporter family. The gene encodes a transmembrane glycoprotein that localizes to the plasma and mitochondrial membranes and mediates the cellular uptake of nucleosides from the surrounding medium. The protein is categorized as an equilibrative (as opposed to concentrative) transporter that is sensitive to inhibition by nitrobenzylthioinosine (NBMPR). Nucleoside transporters are required for nucleotide synthesis in cells that lack de novo nucleoside synthesis pathways, and are also necessary for the uptake of cytotoxic nucleosides used for cancer and viral chemotherapies. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]

SLC12A4 Gene

solute carrier family 12 (potassium/chloride transporter), member 4

This gene encodes a member of the SLC12A transporter family. The encoded protein mediates the coupled movement of potassium and chloride ions across the plasma membrane. This gene is expressed ubiquitously. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jan 2013]

SLC6A13 Gene

solute carrier family 6 (neurotransmitter transporter), member 13

SLC6A12 Gene

solute carrier family 6 (neurotransmitter transporter), member 12

SLC11A1 Gene

solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1

This gene is a member of the solute carrier family 11 (proton-coupled divalent metal ion transporters) family and encodes a multi-pass membrane protein. The protein functions as a divalent transition metal (iron and manganese) transporter involved in iron metabolism and host resistance to certain pathogens. Mutations in this gene have been associated with susceptibility to infectious diseases such as tuberculosis and leprosy, and inflammatory diseases such as rheumatoid arthritis and Crohn disease. Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only one has been determined. [provided by RefSeq, Jul 2008]

LOC101060052 Gene

zinc transporter ZIP1-like

SLC52A1 Gene

solute carrier family 52 (riboflavin transporter), member 1

Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jan 2013]

SLC52A3 Gene

solute carrier family 52 (riboflavin transporter), member 3

This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]

SLC52A2 Gene

solute carrier family 52 (riboflavin transporter), member 2

This gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia. [provided by RefSeq, Jul 2012]

SLC6A11 Gene

solute carrier family 6 (neurotransmitter transporter), member 11

Gamma-aminobutyric acid (GABA) is a major inhibitory neurotransmitter. GABAergic neurotransmission is terminated by the uptake of GABA into the presynaptic terminal and the surrounding astroglial cells by sodium-dependent transporters, such as SLC6A11 (Borden et al., 1994 [PubMed 7874447]).[supplied by OMIM, Nov 2010]

SLC6A17 Gene

solute carrier family 6 (neutral amino acid transporter), member 17

The SLC6 family of proteins, which includes SLC6A17, acts as specific transporters for neurotransmitters, amino acids, and osmolytes like betaine, taurine, and creatine. SLC6 proteins are sodium cotransporters that derive the energy for solute transport from the electrochemical gradient for sodium ions (Hoglund et al., 2005 [PubMed 16125675]).[supplied by OMIM, Mar 2008]

SLC6A15 Gene

solute carrier family 6 (neutral amino acid transporter), member 15

This gene encodes a member of the solute carrier family 6 protein family which transports neutral amino acids. The encoded protein is thought to play a role in neuronal amino acid transport (PMID: 16185194) and may be associated with major depression (PMID: 21521612). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012]

SLC6A14 Gene

solute carrier family 6 (amino acid transporter), member 14

This gene encodes a member of the solute carrier family 6. Members of this family are sodium and chloride dependent neurotransmitter transporters. The encoded protein transports both neutral and cationic amino acids. This protein may also function as a beta-alanine carrier. Mutations in this gene may be associated with X-linked obesity. A pseudogene of this gene is found on chromosome X.[provided by RefSeq, May 2010]

SLC6A10PB Gene

solute carrier family 6 (neurotransmitter transporter), member 8 pseudogene

SLC32A1 Gene

solute carrier family 32 (GABA vesicular transporter), member 1

The protein encoded by this gene is an integral membrane protein involved in gamma-aminobutyric acid (GABA) and glycine uptake into synaptic vesicles. The encoded protein is a member of amino acid/polyamine transporter family II. [provided by RefSeq, Jul 2008]

SLC7A9 Gene

solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9

This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq, Jul 2011]

LOC105370945 Gene

probable lysosomal cobalamin transporter

SLC2AXP1 Gene

solute carrier family 2 (facilitated glucose transporter), pseudogene 1

SLCO2A1 Gene

solute carrier organic anion transporter family, member 2A1

This gene encodes a prostaglandin transporter that is a member of the 12-membrane-spanning superfamily of transporters. The encoded protein may be involved in mediating the uptake and clearance of prostaglandins in numerous tissues. [provided by RefSeq, Dec 2011]

SLC14A2 Gene

solute carrier family 14 (urea transporter), member 2

The protein encoded by this gene belongs to the urea transporter family. In mammalian cells, urea is the chief end product of nitrogen catabolism, and plays an important role in the urinary concentration mechanism. This protein is expressed in the inner medulla of the kidney, and mediates rapid transepithelial urea transport across the inner medullary collecting duct. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2011]

SLC14A1 Gene

solute carrier family 14 (urea transporter), member 1 (Kidd blood group)

The protein encoded by this gene is a membrane transporter that mediates urea transport in erythrocytes. This gene forms the basis for the Kidd blood group system. [provided by RefSeq, Mar 2009]

SLC13A2 Gene

solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2

SLC13A3 Gene

solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3

Mammalian sodium-dicarboxylate cotransporters transport succinate and other Krebs cycle intermediates. They fall into 2 categories based on their substrate affinity: low affinity and high affinity. Both the low- and high-affinity transporters play an important role in the handling of citrate by the kidneys. The protein encoded by this gene represents the high-affinity form. Alternatively spliced transcript variants encoding different isoforms have been found for this gene, although the full-length nature of some of them have not been characterized yet. [provided by RefSeq, Jul 2008]

SLC13A5 Gene

solute carrier family 13 (sodium-dependent citrate transporter), member 5

This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This family member is a sodium-dependent citrate cotransporter that may regulate metabolic processes. Mutations in this gene cause early infantile epileptic encephalopathy 25. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]

SLC40A1 Gene

solute carrier family 40 (iron-regulated transporter), member 1

The protein encoded by this gene is a cell membrane protein that may be involved in iron export from duodenal epithelial cells. Defects in this gene are a cause of hemochromatosis type 4 (HFE4). [provided by RefSeq, Jul 2008]

CTNS Gene

cystinosin, lysosomal cystine transporter

This gene encodes a seven-transmembrane domain protein that functions to transport cystine out of lysosomes. Its activity is driven by the H+ electrochemical gradient of the lysosomal membrane. Mutations in this gene cause cystinosis, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]

LOC100422510 Gene

solute carrier family 12 (sodium/chloride transporter), member 3 pseudogene

SLC27A5 Gene

solute carrier family 27 (fatty acid transporter), member 5

The protein encoded by this gene is an isozyme of very long-chain acyl-CoA synthetase (VLCS). It is capable of activating very long-chain fatty-acids containing 24- and 26-carbons. It is expressed in liver and associated with endoplasmic reticulum but not with peroxisomes. Its primary role is in fatty acid elongation or complex lipid synthesis rather than in degradation. This gene has a mouse ortholog. [provided by RefSeq, Jul 2008]

SLC27A4 Gene

solute carrier family 27 (fatty acid transporter), member 4

This gene encodes a member of a family of fatty acid transport proteins, which are involved in translocation of long-chain fatty acids cross the plasma membrane. This protein is expressed at high levels on the apical side of mature enterocytes in the small intestine, and appears to be the principal fatty acid transporter in enterocytes. Clinical studies suggest this gene as a candidate gene for the insulin resistance syndrome. Mutations in this gene have been associated with ichthyosis prematurity syndrome. [provided by RefSeq, Apr 2010]

SLC27A6 Gene

solute carrier family 27 (fatty acid transporter), member 6

This gene encodes a member of the fatty acid transport protein family (FATP). FATPs are involved in the uptake of long-chain fatty acids and have unique expression patterns. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

SLC27A3 Gene

solute carrier family 27 (fatty acid transporter), member 3

SLC27A2 Gene

solute carrier family 27 (fatty acid transporter), member 2

The protein encoded by this gene is an isozyme of long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. This isozyme activates long-chain, branched-chain and very-long-chain fatty acids containing 22 or more carbons to their CoA derivatives. It is expressed primarily in liver and kidney, and is present in both endoplasmic reticulum and peroxisomes, but not in mitochondria. Its decreased peroxisomal enzyme activity is in part responsible for the biochemical pathology in X-linked adrenoleukodystrophy. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009]

SLC7A8 Gene

solute carrier family 7 (amino acid transporter light chain, L system), member 8

SLC7A7 Gene

solute carrier family 7 (amino acid transporter light chain, y+L system), member 7

The protein encoded by this gene is the light subunit of a cationic amino acid transporter. This sodium-independent transporter is formed when the light subunit encoded by this gene dimerizes with the heavy subunit transporter protein SLC3A2. This transporter is found in epithelial cell membranes where it transfers cationic and large neutral amino acids from the cell to the extracellular space. Defects in this gene are a cause of lysinuric protein intolerance (LPI). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2011]

SLC7A5 Gene

solute carrier family 7 (amino acid transporter light chain, L system), member 5

SLC7A2 Gene

solute carrier family 7 (cationic amino acid transporter, y+ system), member 2

The protein encoded by this gene is a cationic amino acid transporter and a member of the APC (amino acid-polyamine-organocation) family of transporters. The encoded membrane protein is responsible for the cellular uptake of arginine, lysine and ornithine. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

SLC7A3 Gene

solute carrier family 7 (cationic amino acid transporter, y+ system), member 3

This gene encodes a member of the solute carrier family 7. The encoded protein is a sodium-independent cationic amino acid transporter. Alternate splicing results in multiple transcripts that encoded the same protein.[provided by RefSeq, May 2010]

LOC100128093 Gene

magnesium transporter 1 pseudogene

LOC100422417 Gene

solute carrier family 6 (amino acid transporter), member 14 pseudogene

SLCO5A1 Gene

solute carrier organic anion transporter family, member 5A1

This gene encodes a 12 transmembrane domain protein that is a member of the solute carrier organic anion transporter superfamily. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]

LOC105369259 Gene

putative L-type amino acid transporter 1-like protein MLAS

SLC28A1 Gene

solute carrier family 28 (concentrative nucleoside transporter), member 1

SLC22A18AS Gene

solute carrier family 22 (organic cation transporter), member 18 antisense

SLCO1C1 Gene

solute carrier organic anion transporter family, member 1C1

This gene encodes a member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of thyroid hormones in brain tissues. This protein has particularly high affinity for the thyroid hormones thyroxine, tri-iodothyronine and reverse tri-iodothyronine. Polymorphisms in the gene encoding this protein may be associated with fatigue and depression in patients suffering from hyperthyroidism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2009]

SLC22A5 Gene

solute carrier family 22 (organic cation/carnitine transporter), member 5

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015]

SLC19A2 Gene

solute carrier family 19 (thiamine transporter), member 2

This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. [provided by RefSeq, Jul 2008]

SLC19A3 Gene

solute carrier family 19 (thiamine transporter), member 3

This gene encodes a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity. Mutations in this gene cause biotin-responsive basal ganglia disease (BBGD); a recessive disorder manifested in childhood that progresses to chronic encephalopathy, dystonia, quadriparesis, and death if untreated. Patients with BBGD have bilateral necrosis in the head of the caudate nucleus and in the putamen. Administration of high doses of biotin in the early progression of the disorder eliminates pathological symptoms while delayed treatment results in residual paraparesis, mild mental retardation, or dystonia. Administration of thiamine is ineffective in the treatment of this disorder. Experiments have failed to show that this protein can transport biotin. Mutations in this gene also cause a Wernicke's-like encephalopathy.[provided by RefSeq, Jan 2010]

SLC19A1 Gene

solute carrier family 19 (folate transporter), member 1

The membrane protein encoded by this gene is a transporter of folate and is involved in the regulation of intracellular concentrations of folate. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2011]

SLC25A28 Gene

solute carrier family 25 (mitochondrial iron transporter), member 28

SLC25A15P1 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 1

SLC25A15P2 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 2

SLC25A15P3 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 3

SLC25A15P5 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 5

SLCO6A1 Gene

solute carrier organic anion transporter family, member 6A1

LOC100129483 Gene

solute carrier family 35 (GDP-fucose transporter), member C2 pseudogene

SLC27A1 Gene

solute carrier family 27 (fatty acid transporter), member 1

LOC284379 Gene

solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 pseudogene

SLC2A10 Gene

solute carrier family 2 (facilitated glucose transporter), member 10

This gene encodes a member of the class III facilitative glucose transporter family. The encoded protein plays a role in regulation of glucose homeostasis. Mutations in this gene have been associated with arterial tortuosity syndrome.[provided by RefSeq, Dec 2009]

SLC22A4 Gene

solute carrier family 22 (organic cation/zwitterion transporter), member 4

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is an organic cation transporter and plasma integral membrane protein containing eleven putative transmembrane domains as well as a nucleotide-binding site motif. Transport by this protein is at least partially ATP-dependent. [provided by RefSeq, Jul 2008]

SLC22A6 Gene

solute carrier family 22 (organic anion transporter), member 6

The protein encoded by this gene is involved in the sodium-dependent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and may be localized to the basolateral membrane. Four transcript variants encoding four different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SLC22A7 Gene

solute carrier family 22 (organic anion transporter), member 7

The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

SLC22A3 Gene

solute carrier family 22 (organic cation transporter), member 3

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. [provided by RefSeq, Jul 2008]

SLC22A9 Gene

solute carrier family 22 (organic anion transporter), member 9

RTP4 Gene

receptor (chemosensory) transporter protein 4

RTP5 Gene

receptor (chemosensory) transporter protein 5 (putative)

RTP2 Gene

receptor (chemosensory) transporter protein 2

RTP3 Gene

receptor (chemosensory) transporter protein 3

RTP1 Gene

receptor (chemosensory) transporter protein 1

LOC102724223 Gene

sodium- and chloride-dependent creatine transporter 1-like

SLC39A12 Gene

solute carrier family 39 (zinc transporter), member 12

Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A12 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Aug 2008]

SLC39A13 Gene

solute carrier family 39 (zinc transporter), member 13

This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome.[provided by RefSeq, Mar 2010]

SLC39A10 Gene

solute carrier family 39 (zinc transporter), member 10

Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A10 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008]

SLC39A14 Gene

solute carrier family 39 (zinc transporter), member 14

Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A14 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008]

SLC37A2 Gene

solute carrier family 37 (glucose-6-phosphate transporter), member 2

SLC37A4 Gene

solute carrier family 37 (glucose-6-phosphate transporter), member 4

This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants.[provided by RefSeq, Aug 2009]

ASNA1 Gene

arsA arsenite transporter, ATP-binding, homolog 1 (bacterial)

This gene represents the human homolog of the bacterial arsA gene, encoding the arsenite-stimulated ATPase component of the arsenite transporter responsible for resistance to arsenicals. This protein is also a central component of a transmembrane domain (TMD) recognition complex (TRC) that is involved in the post-translational delivery of tail-anchored (TA) proteins from the cytosol to the endoplasmic reticulum (ER). It recognizes and selectively binds the TMD of TA proteins in the cytosol, and delivers them to the ER for insertion. [provided by RefSeq, Oct 2011]

SLC43A2 Gene

solute carrier family 43 (amino acid system L transporter), member 2

System L amino acid transporters, such as SLC43A2, mediate sodium-independent transport of bulky neutral amino acids across cell membranes (Bodoy et al., 2005 [PubMed 15659399]).[supplied by OMIM, Mar 2008]

SLC43A1 Gene

solute carrier family 43 (amino acid system L transporter), member 1

SLC43A1 belongs to the system L family of plasma membrane carrier proteins that transports large neutral amino acids (Babu et al., 2003 [PubMed 12930836]).[supplied by OMIM, Mar 2008]

SLC44A1 Gene

solute carrier family 44 (choline transporter), member 1

SLC44A2 Gene

solute carrier family 44 (choline transporter), member 2

SLC35B3 Gene

solute carrier family 35 (adenosine 3'-phospho 5'-phosphosulfate transporter), member B3

This gene is a member of the solute carrier family. The encoded protein is involved in the transport of 3-prime phosphoadenosine 5-prime phosphosulfate (PAPS) from the nucleus or the cytosol to the Golgi lumen. This gene has been reported to be expressed preferentially in the human colon tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

SLC35B2 Gene

solute carrier family 35 (adenosine 3'-phospho 5'-phosphosulfate transporter), member B2

Sulfotransferases (e.g., SULT4A1; MIM 608359) use an activated form of sulfate, 3-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS), as a common sulfate donor for sulfation of glycoproteins, proteoglycans, and glycolipids in the endoplasmic reticulum and Golgi apparatus. SLC35B2 is located in the microsomal membrane and transports PAPS from the cytosol, where it is synthesized, into the Golgi lumen (Kamiyama et al., 2003 [PubMed 12716889]).[supplied by OMIM, Mar 2008]

SLC35B4 Gene

solute carrier family 35 (UDP-xylose/UDP-N-acetylglucosamine transporter), member B4

Glycosyltransferases, such as SLC35B4, transport nucleotide sugars from the cytoplasm where they are synthesized, to the Golgi apparatus where they are utilized in the synthesis of glycoproteins, glycolipids, and proteoglycans (Ashikov et al., 2005 [PubMed 15911612]).[supplied by OMIM, Mar 2008]

ATP8B3 Gene

ATPase, aminophospholipid transporter, class I, type 8B, member 3

The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to the other. This gene encodes member 3 of phospholipid-transporting ATPase 8B; other members of this protein family are located on chromosomes 1, 15 and 18. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]

ATP8B2 Gene

ATPase, aminophospholipid transporter, class I, type 8B, member 2

The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

ATP8B1 Gene

ATPase, aminophospholipid transporter, class I, type 8B, member 1

This gene encodes a member of the P-type cation transport ATPase family, which belongs to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. Mutations in this gene may result in progressive familial intrahepatic cholestasis type 1 and in benign recurrent intrahepatic cholestasis. [provided by RefSeq, Jul 2008]

SLC25A1P4 Gene

solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1 pseudogene 4

SLC25A1P5 Gene

solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1 pseudogene 5

SLC25A1P1 Gene

solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1 pseudogene 1

SLC25A1P2 Gene

solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1 pseudogene 2

SLC25A1P3 Gene

solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1 pseudogene 3

ATP8A2P2 Gene

ATPase, aminophospholipid transporter, class I, type 8A, member 2 pseudogene 2

SLC28A2 Gene

solute carrier family 28 (concentrative nucleoside transporter), member 2

SLC28A3 Gene

solute carrier family 28 (concentrative nucleoside transporter), member 3

Nucleoside transporters, such as SLC28A3, regulate multiple cellular processes, including neurotransmission, vascular tone, adenosine concentration in the vicinity of cell surface receptors, and transport and metabolism of nucleoside drugs. SLC28A3 shows broad specificity for pyrimidine and purine nucleosides (Ritzel et al., 2001 [PubMed 11032837]).[supplied by OMIM, Mar 2008]

SLCO1B1 Gene

solute carrier organic anion transporter family, member 1B1

This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of numerous endogenous compounds including bilirubin, 17-beta-glucuronosyl estradiol and leukotriene C4. This protein is also involved in the removal of drug compounds such as statins, bromosulfophthalein and rifampin from the blood into the hepatocytes. Polymorphisms in the gene encoding this protein are associated with impaired transporter function. [provided by RefSeq, Mar 2009]

SLC3A2 Gene

solute carrier family 3 (amino acid transporter heavy chain), member 2

This gene is a member of the solute carrier family and encodes a cell surface, transmembrane protein. The protein exists as the heavy chain of a heterodimer, covalently bound through di-sulfide bonds to one of several possible light chains. The encoded transporter plays a role in regulation of intracellular calcium levels and transports L-type amino acids. Alternatively spliced transcript variants, encoding different isoforms, have been characterized. [provided by RefSeq, Nov 2010]

SLC3A1 Gene

solute carrier family 3 (amino acid transporter heavy chain), member 1

This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]

SLC2A14 Gene

solute carrier family 2 (facilitated glucose transporter), member 14

Members of the glucose transporter (GLUT) family, including SLC2A14, are highly conserved integral membrane proteins that transport hexoses such as glucose and fructose into all mammalian cells. GLUTs show tissue and cell-type specific expression (Wu and Freeze, 2002 [PubMed 12504846]).[supplied by OMIM, Mar 2008]

SLC2A13 Gene

solute carrier family 2 (facilitated glucose transporter), member 13

SLC2A12 Gene

solute carrier family 2 (facilitated glucose transporter), member 12

SLC2A12 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Rogers et al., 2002). This family of transporters show conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]

SLC2A11 Gene

solute carrier family 2 (facilitated glucose transporter), member 11

This gene belongs to a family of proteins that mediate the transport of sugars across the cell membrane. The encoded protein transports glucose and fructose. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

FCGRT Gene

Fc fragment of IgG, receptor, transporter, alpha

This gene encodes a receptor that binds the Fc region of monomeric immunoglobulin G. The encoded protein transfers immunoglobulin G antibodies from mother to fetus across the placenta. This protein also binds immunoglobulin G to protect the antibody from degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009]

SLCO4C1 Gene

solute carrier organic anion transporter family, member 4C1

SLCO4C1 belongs to the organic anion transporter (OATP) family. OATPs are involved in the membrane transport of bile acids, conjugated steroids, thyroid hormone, eicosanoids, peptides, and numerous drugs in many tissues (Mikkaichi et al., 2004 [PubMed 14993604]).[supplied by OMIM, Mar 2008]

SLC39A8 Gene

solute carrier family 39 (zinc transporter), member 8

This gene encodes a member of the SLC39 family of solute-carrier genes, which show structural characteristics of zinc transporters. The encoded protein is glycosylated and found in the plasma membrane and mitochondria, and functions in the cellular import of zinc at the onset of inflammation. It is also thought to be the primary transporter of the toxic cation cadmium, which is found in cigarette smoke. Multiple transcript variants encoding different isoforms have been found for this gene. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Oct 2008]

SLC39A1 Gene

solute carrier family 39 (zinc transporter), member 1

This gene encodes a member of the zinc-iron permease family. The encoded protein is localized to the cell membrane and acts as a zinc uptake transporter. This gene has been linked to prostate cancer, breast cancer, and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]

SLC39A2 Gene

solute carrier family 39 (zinc transporter), member 2

This gene encodes a member of the ZIP family of metal ion transporters. The encoded protein functions as a zinc transporter. Mutations in this gene may be associated with susceptibility to carotid artery disease. Multiple transcript variants have been described. [provided by RefSeq, Mar 2010]

SLC39A3 Gene

solute carrier family 39 (zinc transporter), member 3

SLC39A4 Gene

solute carrier family 39 (zinc transporter), member 4

This gene encodes a member of the zinc/iron-regulated transporter-like protein (ZIP) family. The encoded protein localizes to cell membranes and is required for zinc uptake in the intestine. Mutations in this gene result in acrodermatitis enteropathica. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013]

SLC39A5 Gene

solute carrier family 39 (zinc transporter), member 5

The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

SLC39A6 Gene

solute carrier family 39 (zinc transporter), member 6

Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A6 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008]

SLC39A7 Gene

solute carrier family 39 (zinc transporter), member 7

The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

SLC23A1 Gene

solute carrier family 23 (ascorbic acid transporter), member 1

The absorption of vitamin C into the body and its distribution to organs requires two sodium-dependent vitamin C transporters. This gene encodes one of the two transporters. The encoded protein is active in bulk vitamin C transport involving epithelial surfaces. Previously, this gene had an official symbol of SLC23A2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

SLC20A2 Gene

solute carrier family 20 (phosphate transporter), member 2

This gene encodes a member of the inorganic phosphate transporter family. The encoded protein is a type 3 sodium-dependent phosphate symporter that plays an important role in phosphate homeostasis by mediating cellular phosphate uptake. The encoded protein also confers susceptibility to viral infection as a gamma-retroviral receptor. Mutations in this gene may play a role in familial idiopathic basal ganglia calcification. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Mar 2012]

SLC20A1 Gene

solute carrier family 20 (phosphate transporter), member 1

The protein encoded by this gene is a sodium-phosphate symporter that absorbs phosphate from interstitial fluid for use in cellular functions such as metabolism, signal transduction, and nucleic acid and lipid synthesis. The encoded protein is also a retroviral receptor, causing human cells to be susceptible to infection by gibbon ape leukemia virus, simian sarcoma-associated virus, feline leukemia virus subgroup B, and 10A1 murine leukemia virus.[provided by RefSeq, Mar 2011]

SLC30A9 Gene

solute carrier family 30 (zinc transporter), member 9

SLC30A8 Gene

solute carrier family 30 (zinc transporter), member 8

The protein encoded by this gene is a zinc efflux transporter involved in the accumulation of zinc in intracellular vesicles. This gene is expressed at a high level only in the pancreas, particularly in islets of Langerhans. The encoded protein colocalizes with insulin in the secretory pathway granules of the insulin-secreting INS-1 cells. Allelic variants of this gene exist that confer susceptibility to diabetes mellitus, noninsulin-dependent (NIDDM). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]

SLC30A5 Gene

solute carrier family 30 (zinc transporter), member 5

This gene encodes a member of the SLC30A/ZnT family of zinc transporter proteins. ZnT proteins mediate both cellular zinc efflux and zinc sequestration into membrane-bound organelles. The encoded protein plays a role in the early secretory pathway as a heterodimer with zinc transporter 6, and may also regulate zinc sequestration into secretory granules of pancreatic beta cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Oct 2011]

SLC30A4 Gene

solute carrier family 30 (zinc transporter), member 4

Zinc is the second most abundant trace metal in the human body. It is an essential element, serving both a structural role, as in the formation of zinc fingers in DNA-binding proteins, and a catalytic role in metalloenzymes, such as pancreatic carboxypeptidases (e.g., MIM 114852), alkaline phosphatases (e.g., MIM 171760), various dehydrogenases, and superoxide dismutases (e.g., MIM 147450). SLC30A4, or ZNT4, belongs to the ZNT family of zinc transporters. ZNTs are involved in transporting zinc out of the cytoplasm and have similar structures, consisting of 6 transmembrane domains and a histidine-rich cytoplasmic loop (Huang and Gitschier, 1997 [PubMed 9354792]).[supplied by OMIM, Mar 2008]

SLC30A7 Gene

solute carrier family 30 (zinc transporter), member 7

Zinc functions as a cofactor for numerous enzymes, nuclear factors, and hormones and as an intra- and intercellular signal ion. Members of the zinc transporter (ZNT)/SLC30 subfamily of the cation diffusion facilitator family, such as SLC30A7, permit cellular efflux of zinc (Seve et al., 2004 [PubMed 15154973]).[supplied by OMIM, Mar 2008]

SLC30A6 Gene

solute carrier family 30 (zinc transporter), member 6

Zinc functions as a cofactor for numerous enzymes, nuclear factors, and hormones and as an intra- and intercellular signal ion. Members of the zinc transporter (ZNT)/SLC30 subfamily of the cation diffusion facilitator family, such as SLC30A6, permit cellular efflux of zinc (Seve et al., 2004 [PubMed 15154973]).[supplied by OMIM, Mar 2008]

SLC30A1 Gene

solute carrier family 30 (zinc transporter), member 1

SLC30A3 Gene

solute carrier family 30 (zinc transporter), member 3

SLC30A2 Gene

solute carrier family 30 (zinc transporter), member 2

LOC100422432 Gene

solute carrier family 6 (amino acid transporter), member 14 pseudogene

SLC16A8 Gene

solute carrier family 16 (monocarboxylate transporter), member 8

SLC16A8 is a member of a family of proton-coupled monocarboxylate transporters that mediate lactate transport across cell membranes (Yoon et al., 1999 [PubMed 10493836]).[supplied by OMIM, Apr 2010]

SLC16A1 Gene

solute carrier family 16 (monocarboxylate transporter), member 1

The protein encoded by this gene is a proton-linked monocarboxylate transporter that catalyzes the movement of many monocarboxylates, such as lactate and pyruvate, across the plasma membrane. Mutations in this gene are associated with erythrocyte lactate transporter defect. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2009]

SLC16A3 Gene

solute carrier family 16 (monocarboxylate transporter), member 3

Lactic acid and pyruvate transport across plasma membranes is catalyzed by members of the proton-linked monocarboxylate transporter (MCT) family, which has been designated solute carrier family-16. Each MCT appears to have slightly different substrate and inhibitor specificities and transport kinetics, which are related to the metabolic requirements of the tissues in which it is found. The MCTs, which include MCT1 (SLC16A1; MIM 600682) and MCT2 (SLC16A7; MIM 603654), are characterized by 12 predicted transmembrane domains (Price et al., 1998 [PubMed 9425115]).[supplied by OMIM, Mar 2008]

SLC16A2 Gene

solute carrier family 16, member 2 (thyroid hormone transporter)

This gene encodes an integral membrane protein that functions as a transporter of thyroid hormone. The encoded protein facilitates the cellular importation of thyroxine (T4), triiodothyronine (T3), reverse triiodothyronine (rT3) and diidothyronine (T2). This gene is expressed in many tissues and likely plays an important role in the development of the central nervous system. Loss of function mutations in this gene are associated with psychomotor retardation in males while females exhibit no neurological defects and more moderate thyroid-deficient phenotypes. This gene is subject to X-chromosome inactivation. Mutations in this gene are the cause of Allan-Herndon-Dudley syndrome. [provided by RefSeq, Mar 2012]

SLC16A7 Gene

solute carrier family 16 (monocarboxylate transporter), member 7

This gene is a member of the monocarboxylate transporter family. Members in this family transport metabolites, such as lactate, pyruvate, and ketone bodies. The protein encoded by this gene catalyzes the proton-linked transport of monocarboxylates and has the highest affinity for pyruvate. This protein has been reported to be more highly expressed in prostate and colorectal cancer specimens when compared to control specimens. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]

SLC15A2 Gene

solute carrier family 15 (oligopeptide transporter), member 2

The mammalian kidney expresses a proton-coupled peptide transporter that is responsible for the absorption of small peptides, as well as beta-lactam antibiotics and other peptide-like drugs, from the tubular filtrate. This transporter, SLC15A2, belongs to the same gene family as SLC15A1 (MIM 600544), the proton-coupled peptide transporter found in the small intestine (Liu et al, 1995 [PubMed 7756356]).[supplied by OMIM, Feb 2011]

SLC15A3 Gene

solute carrier family 15 (oligopeptide transporter), member 3

SLC15A1 Gene

solute carrier family 15 (oligopeptide transporter), member 1

This gene encodes an intestinal hydrogen peptide cotransporter that is a member of the solute carrier family 15. The encoded protein is localized to the brush border membrane of the intestinal epithelium and mediates the uptake of di- and tripeptides from the lumen into the enterocytes. This protein plays an important role in the uptake and digestion of dietary proteins. This protein also facilitates the absorption of numerous peptidomimetic drugs. [provided by RefSeq, Apr 2010]

SLC15A4 Gene

solute carrier family 15 (oligopeptide transporter), member 4

SLC22A13 Gene

solute carrier family 22 (organic anion/urate transporter), member 13

This gene encodes a member of the organic-cation transporter family. It is located in a gene cluster with another member of the family, organic cation transporter like 4. The encoded protein is a transmembrane protein involved in the transport of small molecules. This protein can function to mediate urate uptake and is a high affinity nicotinate exchanger in the kidneys and the intestine. [provided by RefSeq, Sep 2008]

SLC20A1P1 Gene

solute carrier family 20 (phosphate transporter), member 1 pseudogene 1

SLC20A1P3 Gene

solute carrier family 20 (phosphate transporter), member 1 pseudogene 3

SLC20A1P2 Gene

solute carrier family 20 (phosphate transporter), member 1 pseudogene 2

ATP8A2 Gene

ATPase, aminophospholipid transporter, class I, type 8A, member 2

ATP8A1 Gene

ATPase, aminophospholipid transporter (APLT), class I, type 8A, member 1

The P-type adenosinetriphosphatases (P-type ATPases) are a family of proteins which use the free energy of ATP hydrolysis to drive uphill transport of ions across membranes. Several subfamilies of P-type ATPases have been identified. One subfamily catalyzes transport of heavy metal ions. Another subfamily transports non-heavy metal ions (NMHI). The protein encoded by this gene is a member of the third subfamily of P-type ATPases and acts to transport amphipaths, such as phosphatidylserine. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SLC16A10 Gene

solute carrier family 16 (aromatic amino acid transporter), member 10

SLC16A10 is a member of a family of plasma membrane amino acid transporters that mediate the Na(+)-independent transport of aromatic amino acids across the plasma membrane.[supplied by OMIM, Apr 2004]

SLC46A1 Gene

solute carrier family 46 (folate transporter), member 1

This gene encodes a transmembrane proton-coupled folate transporter protein that facilitates the movement of folate and antifolate substrates across cell membranes, optimally in acidic pH environments. This protein is also expressed in the brain and choroid plexus where it transports folates into the central nervous system. This protein further functions as a heme transporter in duodenal enterocytes, and potentially in other tissues like liver and kidney. Its localization to the apical membrane or cytoplasm of intestinal cells is modulated by dietary iron levels. Mutations in this gene are associated with autosomal recessive hereditary folate malabsorption disease. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2013]

CUTC Gene

cutC copper transporter

Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar 2008]

SLC6A3 Gene

solute carrier family 6 (neurotransmitter transporter), member 3

This gene encodes a dopamine transporter which is a member of the sodium- and chloride-dependent neurotransmitter transporter family. The 3' UTR of this gene contains a 40 bp tandem repeat, referred to as a variable number tandem repeat or VNTR, which can be present in 3 to 11 copies. Variation in the number of repeats is associated with idiopathic epilepsy, attention-deficit hyperactivity disorder, dependence on alcohol and cocaine, susceptibility to Parkinson disease and protection against nicotine dependence.[provided by RefSeq, Nov 2009]

SLC6A2 Gene

solute carrier family 6 (neurotransmitter transporter), member 2

This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]

SLC6A1 Gene

solute carrier family 6 (neurotransmitter transporter), member 1

The SLC6A1 gene encodes a gamma-aminobutyric acid (GABA) transporter, which removes GABA from the synaptic cleft (Hirunsatit et al., 2009 [PubMed 19077666]).[supplied by OMIM, Jul 2009]

SLC6A7 Gene

solute carrier family 6 (neurotransmitter transporter), member 7

This gene is a member of the gamma-aminobutyric acid (GABA) neurotransmitter gene family and encodes a high-affinity mammalian brain L-proline transporter protein. This transporter protein differs from other sodium-dependent plasma membrane carriers by its pharmacological specificity, kinetic properties, and ionic requirements. [provided by RefSeq, Jul 2008]

SLC6A6 Gene

solute carrier family 6 (neurotransmitter transporter), member 6

This gene encodes a multi-pass membrane protein that is a member of a family of sodium and chloride-ion dependent transporters. The encoded protein transports taurine and beta-alanine. There is a pseudogene for this gene on chromosome 21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]

SLC6A5 Gene

solute carrier family 6 (neurotransmitter transporter), member 5

This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia; a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. [provided by RefSeq, Oct 2009]

SLC6A4 Gene

solute carrier family 6 (neurotransmitter transporter), member 4

This gene encodes an integral membrane protein that transports the neurotransmitter serotonin from synaptic spaces into presynaptic neurons. The encoded protein terminates the action of serotonin and recycles it in a sodium-dependent manner. This protein is a target of psychomotor stimulants, such as amphetamines and cocaine, and is a member of the sodium:neurotransmitter symporter family. A repeat length polymorphism in the promoter of this gene has been shown to affect the rate of serotonin uptake and may play a role in sudden infant death syndrome, aggressive behavior in Alzheimer disease patients, and depression-susceptibility in people experiencing emotional trauma. [provided by RefSeq, Jul 2008]

SLC6A9 Gene

solute carrier family 6 (neurotransmitter transporter, glycine), member 9

SLC6A8 Gene

solute carrier family 6 (neurotransmitter transporter), member 8

The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

SLC7A5P1 Gene

solute carrier family 7 (amino acid transporter light chain, L system), member 5 pseudogene 1

This locus represents a transcribed pseudogene of the L-type amino acid transporter 1. [provided by RefSeq, Jul 2008]

SLC7A5P2 Gene

solute carrier family 7 (amino acid transporter light chain, L system), member 5 pseudogene 2

SLC25A15P4 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 pseudogene 4

SLCO3A1 Gene

solute carrier organic anion transporter family, member 3A1

LOC100422614 Gene

solute carrier family 7 (anionic amino acid transporter), member 13 pseudogene

LOC100422610 Gene

solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 pseudogene

SLC6A19 Gene

solute carrier family 6 (neutral amino acid transporter), member 19

This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]

SLC6A18 Gene

solute carrier family 6 (neutral amino acid transporter), member 18

The SLC6 family of proteins, which includes SLC6A18, act as specific transporters for neurotransmitters, amino acids, and osmolytes like betaine, taurine, and creatine. SLC6 proteins are sodium cotransporters that derive the energy for solute transport from the electrochemical gradient for sodium ions (Hoglund et al., 2005 [PubMed 16125675]).[supplied by OMIM, Apr 2010]

SLC33A1 Gene

solute carrier family 33 (acetyl-CoA transporter), member 1

The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]

LOC101060604 Gene

putative L-type amino acid transporter 1-like protein IMAA

SLCO1B3 Gene

solute carrier organic anion transporter family, member 1B3

This gene encodes a liver-specific member of the organic anion transporter family. The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of endogenous and xenobiotic compounds and plays a critical role in bile acid and bilirubin transport. Mutations in this gene are a cause of Rotor type hyperbilirubinemia. [provided by RefSeq, Feb 2012]

SLCO1B7 Gene

solute carrier organic anion transporter family, member 1B7 (non-functional)

SLC22A16 Gene

solute carrier family 22 (organic cation/carnitine transporter), member 16

This gene encodes a member of the organic zwitterion transporter protein family which transports carnitine. The encoded protein has also been shown to transport anticancer drugs like bleomycin (PMID: 20037140) successful treatment has been correlated with the level of activity of this transporter in tumor cells. [provided by RefSeq, Dec 2011]

SLC22A12 Gene

solute carrier family 22 (organic anion/urate transporter), member 12

The protein encoded by this gene is a member of the organic anion transporter (OAT) family, and it acts as a urate transporter to regulate urate levels in blood. This protein is an integral membrane protein primarily found in epithelial cells of the proximal tubule of the kidney. An elevated level of serum urate, hyperuricemia, is associated with increased incidences of gout, and mutations in this gene cause renal hypouricemia type 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]

SLC22A11 Gene

solute carrier family 22 (organic anion/urate transporter), member 11

The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]

SLC4A11 Gene

solute carrier family 4, sodium borate transporter, member 11

This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]

SLC4A10 Gene

solute carrier family 4, sodium bicarbonate transporter, member 10

This gene belongs to a small family of sodium-coupled bicarbonate transporters (NCBTs) that regulate the intracellular pH of neurons, the secretion of bicarbonate ions across the choroid plexus, and the pH of the brain extracellular fluid. The protein encoded by this gene was initially identified as a sodium-driven chloride bicarbonate exchanger (NCBE) though there is now evidence that its sodium/bicarbonate cotransport activity is independent of any chloride ion countertransport under physiological conditions. This gene is now classified as a member A10 of the SLC4 family of transmembrane solute carriers. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, May 2010]

LOC100462652 Gene

solute carrier family 6 (amino acid transporter), member 14 pseudogene

SLC35D2 Gene

solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2

Nucleotide sugars, which are synthesized in the cytosol or the nucleus, are high-energy donor substrates for glycosyltransferases located in the lumen of the endoplasmic reticulum and Golgi apparatus. Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters, such as SLC35D2 (Suda et al., 2004 [PubMed 15082721]).[supplied by OMIM, Mar 2008]

SLC35D1 Gene

solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1

Glycosylation of cellular glycoconjugates occurs in the endoplasmic reticulum (ER) and Golgi compartment, and requires transport of nucleotide sugars from the cytosol into the lumen of the ER and Golgi by specific transporters. The protein encoded by this gene resides in the ER, and transports both UDP-glucuronic acid (UDP-GlcA) and UDP-N-acetylgalactosamine (UDP-GalNAc) from the cytoplasm to the ER lumen. It may participate in glucuronidation and/or chondroitin sulfate biosynthesis. Mutations in this gene are associated with Schneckenbecken dysplasia.[provided by RefSeq, Sep 2009]

SLC16A5 Gene

solute carrier family 16 (monocarboxylate transporter), member 5

This gene encodes a member of the monocarboxylate transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

SLC25A15 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15

This gene is a member of the mitochondrial carrier family. The encoded protein transports ornithine across the inner mitochondrial membrane from the cytosol to the mitochondrial matrix. The protein is an essential component of the urea cycle, and functions in ammonium detoxification and biosynthesis of the amino acid arginine. Mutations in this gene result in hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. There is a pseudogene of this locus on the Y chromosome.[provided by RefSeq, May 2009]

SLC25A10 Gene

solute carrier family 25 (mitochondrial carrier; dicarboxylate transporter), member 10

This gene encodes a member of a family of proteins that translocate small metabolites across the mitochondrial membrane. The encoded protein exchanges dicarboxylates, such as malate and succinate, for phosphate, sulfate, and other small molecules, thereby providing substrates for metabolic processes including the Krebs cycle and fatty acid synthesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]

SLC50A1 Gene

solute carrier family 50 (sugar efflux transporter), member 1

MMGT1 Gene

membrane magnesium transporter 1

LOC100131725 Gene

solute carrier family 39 (zinc transporter), member 14 pseudogene

LOC100533846 Gene

solute carrier family 30 (zinc transporter), member 5 pseudogene

SLCO4A1 Gene

solute carrier organic anion transporter family, member 4A1

MRS2 Gene

MRS2 magnesium transporter

SLC12A5 Gene

solute carrier family 12 (potassium/chloride transporter), member 5

K-Cl cotransporters are proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The protein encoded by this gene is an integral membrane K-Cl cotransporter that can function in either a net efflux or influx pathway, depending on the chemical concentration gradients of potassium and chloride. The encoded protein can act as a homomultimer, or as a heteromultimer with other K-Cl cotransporters, to maintain chloride homeostasis in neurons. Alternative splicing results in two transcript variants encoding different isoforms. [provided by RefSeq, Sep 2008]

SLC12A7 Gene

solute carrier family 12 (potassium/chloride transporter), member 7

SLC12A6 Gene

solute carrier family 12 (potassium/chloride transporter), member 6

This gene is a member of the K-Cl cotransporter (KCC) family. K-Cl cotransporters are integral membrane proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The proteins encoded by this gene are activated by cell swelling induced by hypotonic conditions. Alternate splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy. [provided by RefSeq, Jul 2008]

SLC12A1 Gene

solute carrier family 12 (sodium/potassium/chloride transporter), member 1

This gene encodes a kidney-specific sodium-potassium-chloride cotransporter that is expressed on the luminal membrane of renal epithelial cells of the thick ascending limb of Henle's loop and the macula densa. It plays a key role in concentrating urine and accounts for most of the NaCl resorption. It is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their biological validity in humans has not been experimentally proven.[provided by RefSeq, May 2010]

SLC12A3 Gene

solute carrier family 12 (sodium/chloride transporter), member 3

This gene encodes a renal thiazide-sensitive sodium-chloride cotransporter that is important for electrolyte homeostasis. This cotransporter mediates sodium and chloride reabsorption in the distal convoluted tubule. Mutations in this gene cause Gitelman syndrome, a disease similar to Bartter's syndrome, that is characterized by hypokalemic alkalosis combined with hypomagnesemia, low urinary calcium, and increased renin activity associated with normal blood pressure. This cotransporter is the target for thiazide diuretics that are used for treating high blood pressure. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SLC12A2 Gene

solute carrier family 12 (sodium/potassium/chloride transporter), member 2

The protein encoded by this gene mediates sodium and chloride transport and reabsorption. The encoded protein is a membrane protein and is important in maintaining proper ionic balance and cell volume. This protein is phosphorylated in response to DNA damage. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]

SLC11A2 Gene

solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2

This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]

LOC402269 Gene

equilibrative nucleoside transporter 4-like

SLC35A1 Gene

solute carrier family 35 (CMP-sialic acid transporter), member A1

The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]

SLC35A2 Gene

solute carrier family 35 (UDP-galactose transporter), member A2

This gene encodes a member of the nucleotide-sugar transporter family. The encoded protein is a multi-pass membrane protein. It transports UDP-galactose from the cytosol into Golgi vesicles, where it serves as a glycosyl donor for the generation of glycans. Mutations in this gene cause congenital disorder of glycosylation type IIm (CDG2M). Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Oct 2014]

SLC35A3 Gene

solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3

This gene encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane. In cattle, a missense mutation in this gene causes complex vertebral malformation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

SLC41A1 Gene

solute carrier family 41 (magnesium transporter), member 1

SLC41A2 Gene

solute carrier family 41 (magnesium transporter), member 2

SLC22A1 Gene

solute carrier family 22 (organic cation transporter), member 1

Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. This gene is one of three similar cation transporter genes located in a cluster on chromosome 6. The encoded protein contains twelve putative transmembrane domains and is a plasma integral membrane protein. Two transcript variants encoding two different isoforms have been found for this gene, but only the longer variant encodes a functional transporter. [provided by RefSeq, Jul 2008]

SLC22A8 Gene

solute carrier family 22 (organic anion transporter), member 8

This gene encodes a protein involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and appears to be localized to the basolateral membrane of the kidney. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, May 2010]

ATP8A2P3 Gene

ATPase, aminophospholipid transporter, class I, type 8A, member 2 pseudogene 3

ATP8A2P1 Gene

ATPase, aminophospholipid transporter, class I, type 8A, member 2 pseudogene 1

SLC2A3P2 Gene

solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 2

SLC2A3P1 Gene

solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 1

SLC2A3P4 Gene

solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 4

SLC48A1 Gene

solute carrier family 48 (heme transporter), member 1

SLC25A2 Gene

solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2

This intronless gene encodes a protein that localizes to the mitochondrial inner membrane and likely functions as a transporter of small molecules such as ornithine. This gene is located between the protocadherin beta and gamma gene clusters on chromosome 5. [provided by RefSeq, Dec 2014]

SLC25A1 Gene

solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1

This gene encodes a member of the mitochondrial carrier subfamily of solute carrier proteins. Members of this family include nuclear-encoded transporters that translocate small metabolites across the mitochondrial membrane. This protein regulates the movement of citrate across the inner membranes of the mitochondria. Mutations in this gene have been associated with combined D-2- and L-2-hydroxyglutaric aciduria. Pseudogenes of this gene have been identified on chromosomes 7, 11, 16, and 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

SLC1A4 Gene

solute carrier family 1 (glutamate/neutral amino acid transporter), member 4

SLC1A5 Gene

solute carrier family 1 (neutral amino acid transporter), member 5

The SLC1A5 gene encodes a sodium-dependent neutral amino acid transporter that can act as a receptor for RD114/type D retrovirus (Larriba et al., 2001 [PubMed 11781704]).[supplied by OMIM, Jan 2011]

SLC1A6 Gene

solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6

SLC1A7 Gene

solute carrier family 1 (glutamate transporter), member 7

SLC1A1 Gene

solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1

This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]

SLC1A2 Gene

solute carrier family 1 (glial high affinity glutamate transporter), member 2

This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Mutations in and decreased expression of this protein are associated with amyotrophic lateral sclerosis. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Sep 2010]

SLC1A3 Gene

solute carrier family 1 (glial high affinity glutamate transporter), member 3

This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]

SLC2A9 Gene

solute carrier family 2 (facilitated glucose transporter), member 9

This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

SLC2A8 Gene

solute carrier family 2 (facilitated glucose transporter), member 8

This gene belongs to the solute carrier 2A family, which includes intracellular glucose transporters. Based on sequence comparison, the glucose transporters are grouped into three classes and this gene is a member of class II. The encoded protein, like other members of the family, contains several conserved residues and motifs and 12 transmembrane domains with both amino and carboxyl ends being on the cytosolic side of the membrane. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]

SLC2A7 Gene

solute carrier family 2 (facilitated glucose transporter), member 7

SLC2A7 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Li et al., 2004). This family of transporters shows conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]

SLC2A6 Gene

solute carrier family 2 (facilitated glucose transporter), member 6

Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM, Jul 2002]

SLC2A5 Gene

solute carrier family 2 (facilitated glucose/fructose transporter), member 5

SLC2A4 Gene

solute carrier family 2 (facilitated glucose transporter), member 4

This gene is a member of the solute carrier family 2 (facilitated glucose transporter) family and encodes a protein that functions as an insulin-regulated facilitative glucose transporter. In the absence of insulin, this integral membrane protein is sequestered within the cells of muscle and adipose tissue. Within minutes of insulin stimulation, the protein moves to the cell surface and begins to transport glucose across the cell membrane. Mutations in this gene have been associated with noninsulin-dependent diabetes mellitus (NIDDM). [provided by RefSeq, Jul 2008]

SLC2A3 Gene

solute carrier family 2 (facilitated glucose transporter), member 3

SLC2A2 Gene

solute carrier family 2 (facilitated glucose transporter), member 2

This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]

SLC2A1 Gene

solute carrier family 2 (facilitated glucose transporter), member 1

This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Apr 2013]

LOC100130329 Gene

solute carrier family 41 (magnesium transporter), member 2 pseudogene

SLC6A10P Gene

solute carrier family 6 (neurotransmitter transporter), member 10, pseudogene

LOC100420667 Gene

solute carrier family 19 (thiamine transporter), member 3 pseudogene

SLC7A10 Gene

solute carrier family 7 (neutral amino acid transporter light chain, asc system), member 10

SLC7A10, in association with 4F2HC (SLC3A2; MIM 158070), mediates high-affinity transport of D-serine and several other neutral amino acids (Nakauchi et al., 2000 [PubMed 10863037]).[supplied by OMIM, Mar 2008]

SLC7A11 Gene

solute carrier family 7 (anionic amino acid transporter light chain, xc- system), member 11

This gene encodes a member of a heteromeric, sodium-independent, anionic amino acid transport system that is highly specific for cysteine and glutamate. In this system, designated Xc(-), the anionic form of cysteine is transported in exchange for glutamate. This protein has been identified as the predominant mediator of Kaposi sarcoma-associated herpesvirus fusion and entry permissiveness into cells. Also, increased expression of this gene in primary gliomas (compared to normal brain tissue) was associated with increased glutamate secretion via the XCT channels, resulting in neuronal cell death. [provided by RefSeq, Sep 2011]

SLC7A13 Gene

solute carrier family 7 (anionic amino acid transporter), member 13

atp-binding cassette (abc) transporter complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the atp-binding cassette (abc) transporter complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

atp-binding cassette (abc) transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the atp-binding cassette (abc) transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

atp-binding cassette (abc) transporter complex Gene Set

From GO Cellular Component Annotations

proteins localized to the atp-binding cassette (abc) transporter complex cellular component from the curated GO Cellular Component Annotations dataset.

atp-binding cassette (abc) transporter complex, transmembrane substrate-binding subunit-containing Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the atp-binding cassette (abc) transporter complex, transmembrane substrate-binding subunit-containing cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1;MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, ATPAF2 TYPE from the curated CTD Gene-Disease Associations dataset.

ABC transporter A, ABCA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter A, ABCA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter Tap-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter Tap-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter type 1, transmembrane domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter type 1, transmembrane domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC-2 type transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC-2 type transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter, G1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter, G1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ABC transporter ABCE Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC transporter ABCE protein domain from the InterPro Predicted Protein Domain Annotations dataset.

tripartite atp-independent periplasmic transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the tripartite atp-independent periplasmic transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

atp transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the atp transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cassette Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cassette in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ABC-1 Gene Set

From COSMIC Cell Line Gene CNV Profiles

genes with high or low copy number in ABC-1 relative to other cell lines from the COSMIC Cell Line Gene CNV Profiles dataset.

ABC-1 Gene Set

From COSMIC Cell Line Gene Mutation Profiles

genes mutated in the ABC-1 cell line from the COSMIC Cell Line Gene Mutation Profiles dataset.

ABC-1 Gene Set

From GDSC Cell Line Gene Expression Profiles

genes with high or low expression in ABC-1 relative to other cell lines from the GDSC Cell Line Gene Expression Profiles dataset.

abc Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term abc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

ABC-type uncharacterised transport system Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ABC-type uncharacterised transport system protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abc transporters general Gene Set

From KEGG Pathways

proteins participating in the abc transporters general pathway from the KEGG Pathways dataset.

ABC-1 Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles

genes with high or low copy number in ABC-1 relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene CNV Profiles dataset.

ABC-1 Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles

genes with high or low expression in ABC-1 relative to other cell lines from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Expression Profiles dataset.

ABC-1 Gene Set

From Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles

genes mutated in the ABC-1 cell line from the Klijn et al., Nat. Biotechnol., 2015 Cell Line Gene Mutation Profiles dataset.

ABC-family proteins mediated transport Gene Set

From Reactome Pathways

proteins participating in the ABC-family proteins mediated transport pathway from the Reactome Pathways dataset.

Mitochondrial ABC transporters Gene Set

From Reactome Pathways

proteins participating in the Mitochondrial ABC transporters pathway from the Reactome Pathways dataset.

electron transporter, transferring electrons from coqh2-cytochrome c reductase complex and cytochrome c oxidase complex activity Gene Set

From GO Molecular Function Annotations

genes performing the electron transporter, transferring electrons from coqh2-cytochrome c reductase complex and cytochrome c oxidase complex activity molecular function from the curated GO Molecular Function Annotations dataset.

chromatin remodeling by hswi/snf atp-dependent complexes Gene Set

From Biocarta Pathways

proteins participating in the chromatin remodeling by hswi/snf atp-dependent complexes pathway from the Biocarta Pathways dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nuclearly-encoded mitochondrial complex V (ATP synthase) deficiency 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

mitochondrial proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex, catalytic core f(1) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

dna topoisomerase complex (atp-hydrolyzing) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the dna topoisomerase complex (atp-hydrolyzing) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting atp synthase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex, coupling factor f(o) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

atp-sensitive potassium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the atp-sensitive potassium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting atp synthase complex, catalytic core f(1) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting atp synthase complex, coupling factor f(o) cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

atp-sensitive potassium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the atp-sensitive potassium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the proton-transporting atp synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chloroplast atp synthase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chloroplast atp synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial proton-transporting atp synthase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the proton-transporting atp synthase complex, catalytic core f(1) cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the proton-transporting atp synthase complex, coupling factor f(o) cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ATP-utilizing chromatin assembly and remodeling factor (hACF) complex Gene Set

From CORUM Protein Complexes

proteins in the ATP-utilizing chromatin assembly and remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.

proton-transporting atp synthase complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the proton-transporting atp synthase complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial proton-transporting atp synthase complex assembly Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial proton-transporting atp synthase complex assembly biological process from the curated GO Biological Process Annotations dataset.

mitochondrial proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex, catalytic core f(1) cellular component from the curated GO Cellular Component Annotations dataset.

atp-sensitive potassium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the atp-sensitive potassium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

dna topoisomerase complex (atp-hydrolyzing) Gene Set

From GO Cellular Component Annotations

proteins localized to the dna topoisomerase complex (atp-hydrolyzing) cellular component from the curated GO Cellular Component Annotations dataset.

proton-transporting atp synthase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the proton-transporting atp synthase complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex, coupling factor f(o) cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase complex cellular component from the curated GO Cellular Component Annotations dataset.

proton-transporting atp synthase complex, catalytic core f(1) Gene Set

From GO Cellular Component Annotations

proteins localized to the proton-transporting atp synthase complex, catalytic core f(1) cellular component from the curated GO Cellular Component Annotations dataset.

proton-transporting atp synthase complex, coupling factor f(o) Gene Set

From GO Cellular Component Annotations

proteins localized to the proton-transporting atp synthase complex, coupling factor f(o) cellular component from the curated GO Cellular Component Annotations dataset.

decreased activity of mitochondrial atp synthase complex Gene Set

From HPO Gene-Disease Associations

genes associated with the decreased activity of mitochondrial atp synthase complex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

?mitochondrial complex (atp synthase) deficiency, nuclear type 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex (atp synthase) deficiency, nuclear type 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial complex v (atp synthase) deficiency, nuclear type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial complex v (atp synthase) deficiency, nuclear type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mitochondrial complex v (atp synthase) deficiency, nuclear type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

transmembrane transporter complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the transmembrane transporter complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial intermembrane space protein transporter complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

transporter complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the transporter complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

transmembrane transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the transmembrane transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial intermembrane space protein transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

vacuolar transporter chaperone complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the vacuolar transporter chaperone complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

transporter complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the transporter complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

transmembrane transporter complex Gene Set

From GO Cellular Component Annotations

proteins localized to the transmembrane transporter complex cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial intermembrane space protein transporter complex Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial intermembrane space protein transporter complex cellular component from the curated GO Cellular Component Annotations dataset.

transporter complex Gene Set

From GO Cellular Component Annotations

proteins localized to the transporter complex cellular component from the curated GO Cellular Component Annotations dataset.

proton-transporting atp synthase, catalytic core Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the proton-transporting atp synthase, catalytic core cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial proton-transporting atp synthase, catalytic core Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial proton-transporting atp synthase, catalytic core cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

F1F0-ATP synthase (EC 3.6.3.14), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the F1F0-ATP synthase (EC 3.6.3.14), mitochondrial protein complex from the CORUM Protein Complexes dataset.

6-N,N-diethyl-beta,gamma-dibromomethylene-D-ATP Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical 6-N,N-diethyl-beta,gamma-dibromomethylene-D-ATP from the curated CTD Gene-Chemical Interactions dataset.

response heterogeneity of human macrophages to atp Gene Set

From GAD Gene-Disease Associations

genes associated with the disease response heterogeneity of human macrophages to atp in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atp Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term atp in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

atp synthesis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

response to atp Gene Set

From GO Biological Process Annotations

genes participating in the response to atp biological process from the curated GO Biological Process Annotations dataset.

atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations

genes participating in the atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations dataset.

regulation of atp metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atp metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of atp citrate synthase activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atp citrate synthase activity biological process from the curated GO Biological Process Annotations dataset.

atp biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the atp biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of atp:adp antiporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atp:adp antiporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of dna topoisomerase (atp-hydrolyzing) activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of dna topoisomerase (atp-hydrolyzing) activity biological process from the curated GO Biological Process Annotations dataset.

atp-dependent chromatin remodeling Gene Set

From GO Biological Process Annotations

genes participating in the atp-dependent chromatin remodeling biological process from the curated GO Biological Process Annotations dataset.

positive regulation of atp biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of atp biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

cellular response to atp Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to atp biological process from the curated GO Biological Process Annotations dataset.

negative regulation of atp citrate synthase activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of atp citrate synthase activity biological process from the curated GO Biological Process Annotations dataset.

atp transport Gene Set

From GO Biological Process Annotations

genes participating in the atp transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of atp biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of atp biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of atp metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of atp metabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of dna topoisomerase (atp-hydrolyzing) activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of dna topoisomerase (atp-hydrolyzing) activity biological process from the curated GO Biological Process Annotations dataset.

atp hydrolysis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the atp hydrolysis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations dataset.

atp metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the atp metabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of atp metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of atp metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of atp biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of atp biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

mitochondrial atp synthesis coupled proton transport Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrial atp synthesis coupled proton transport biological process from the curated GO Biological Process Annotations dataset.

proton-transporting atp synthase, catalytic core Gene Set

From GO Cellular Component Annotations

proteins localized to the proton-transporting atp synthase, catalytic core cellular component from the curated GO Cellular Component Annotations dataset.

mitochondrial proton-transporting atp synthase, catalytic core Gene Set

From GO Cellular Component Annotations

proteins localized to the mitochondrial proton-transporting atp synthase, catalytic core cellular component from the curated GO Cellular Component Annotations dataset.

atp-dependent polynucleotide kinase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent polynucleotide kinase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-activated inward rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-activated inward rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

proton-transporting atp synthase activity, rotational mechanism Gene Set

From GO Molecular Function Annotations

genes performing the proton-transporting atp synthase activity, rotational mechanism molecular function from the curated GO Molecular Function Annotations dataset.

atp:adp antiporter activity Gene Set

From GO Molecular Function Annotations

genes performing the atp:adp antiporter activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent rna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent rna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

rna ligase (atp) activity Gene Set

From GO Molecular Function Annotations

genes performing the rna ligase (atp) activity molecular function from the curated GO Molecular Function Annotations dataset.

atp citrate synthase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp citrate synthase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-activated nucleotide receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-activated nucleotide receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

sulfate adenylyltransferase (atp) activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfate adenylyltransferase (atp) activity molecular function from the curated GO Molecular Function Annotations dataset.

dna ligase (atp) activity Gene Set

From GO Molecular Function Annotations

genes performing the dna ligase (atp) activity molecular function from the curated GO Molecular Function Annotations dataset.

biotin-[propionyl-coa-carboxylase (atp-hydrolyzing)] ligase activity Gene Set

From GO Molecular Function Annotations

genes performing the biotin-[propionyl-coa-carboxylase (atp-hydrolyzing)] ligase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp:3'-cytidine-cytidine-trna adenylyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp:3'-cytidine-cytidine-trna adenylyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent 5'-3' dna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent 5'-3' dna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

single-stranded dna-dependent atp-dependent dna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the single-stranded dna-dependent atp-dependent dna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent 5'-3' dna/rna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent 5'-3' dna/rna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

5-oxoprolinase (atp-hydrolyzing) activity Gene Set

From GO Molecular Function Annotations

genes performing the 5-oxoprolinase (atp-hydrolyzing) activity molecular function from the curated GO Molecular Function Annotations dataset.

atp diphosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp diphosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

dna topoisomerase type ii (atp-hydrolyzing) activity Gene Set

From GO Molecular Function Annotations

genes performing the dna topoisomerase type ii (atp-hydrolyzing) activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent 5'-3' rna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent 5'-3' rna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent polyribonucleotide 5'-hydroxyl-kinase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent polyribonucleotide 5'-hydroxyl-kinase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent 3'-5' dna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent 3'-5' dna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent nad(p)h-hydrate dehydratase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent nad(p)h-hydrate dehydratase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent peptidase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent peptidase activity molecular function from the curated GO Molecular Function Annotations dataset.

extracellular atp-gated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular atp-gated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent dna/rna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent dna/rna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent microtubule motor activity, plus-end-directed Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent microtubule motor activity, plus-end-directed molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent dna helicase activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent dna helicase activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-dependent microtubule motor activity, minus-end-directed Gene Set

From GO Molecular Function Annotations

genes performing the atp-dependent microtubule motor activity, minus-end-directed molecular function from the curated GO Molecular Function Annotations dataset.

TNP-ATP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the TNP-ATP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

ATPγS Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the ATPγS ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Phosphoribosyl-ATP Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Phosphoribosyl-ATP metabolite from the curated HMDB Metabolites of Enzymes dataset.

ATP-dependent (S)-NAD(P)H-hydrate dehydratase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-dependent (S)-NAD(P)H-hydrate dehydratase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial ATP synthase subunit g, animal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial ATP synthase subunit g, animal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GMP synthetase ATP pyrophosphatase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GMP synthetase ATP pyrophosphatase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/RNA helicase, ATP-dependent, DEAH-box type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-NAD kinase, PpnK-type, all-beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-NAD kinase, PpnK-type, all-beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Synapsin, pre-ATP-grasp domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Synapsin, pre-ATP-grasp domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-grasp fold, subdomain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-grasp fold, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-grasp fold, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-grasp fold, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP synthase subunit s-like protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP synthase subunit s-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-citrate lyase/succinyl-CoA ligase, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-citrate lyase/succinyl-CoA ligase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-dependent Clp protease proteolytic subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-dependent Clp protease proteolytic subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inorganic polyphosphate/ATP-NAD kinase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inorganic polyphosphate/ATP-NAD kinase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-dependent RNA helicase DEAD-box, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-dependent RNA helicase DEAD-box, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-citrate lyase/succinyl-CoA ligase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-citrate lyase/succinyl-CoA ligase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-grasp fold, succinyl-CoA synthetase-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-grasp fold, succinyl-CoA synthetase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

V-type ATP synthase regulatory subunit B/beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the V-type ATP synthase regulatory subunit B/beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-dependent helicase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-dependent helicase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Snf2 ATP coupling domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Snf2 ATP coupling domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP:guanido phosphotransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP:guanido phosphotransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pre-ATP-grasp domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pre-ATP-grasp domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Adenosylcobalamin biosynthesis, ATP:cob(I)alamin adenosyltransferase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adenosylcobalamin biosynthesis, ATP:cob(I)alamin adenosyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA ligase, ATP-dependent, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA ligase, ATP-dependent, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP:guanido phosphotransferase, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP:guanido phosphotransferase, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP:cob(I)alamin adenosyltransferase, PduO-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP:cob(I)alamin adenosyltransferase, PduO-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Mitochondrial F1-F0 ATP synthase subunit F, predicted Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mitochondrial F1-F0 ATP synthase subunit F, predicted protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP synthase subunit alpha-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP synthase subunit alpha-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP synthase subunit s, mitochondrial Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP synthase subunit s, mitochondrial protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-grasp fold Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-grasp fold protein domain from the InterPro Predicted Protein Domain Annotations dataset.

F1F0 ATP synthase OSCP/delta subunit, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the F1F0 ATP synthase OSCP/delta subunit, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA ligase, ATP-dependent, central Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA ligase, ATP-dependent, central protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA helicase, ATP-dependent, RecQ type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA helicase, ATP-dependent, RecQ type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Probable ATP-dependent RNA helicase DDX11/DDX12 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Probable ATP-dependent RNA helicase DDX11/DDX12 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphoribosylglycinamide synthetase, ATP-grasp (A) domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphoribosylglycinamide synthetase, ATP-grasp (A) domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-grasp fold, RimK-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-grasp fold, RimK-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-sulfurylase PUA-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-sulfurylase PUA-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

V-type ATP synthase catalytic alpha chain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the V-type ATP synthase catalytic alpha chain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Histidine-tRNA ligase/ATP phosphoribosyltransferase regulatory subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Histidine-tRNA ligase/ATP phosphoribosyltransferase regulatory subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-cone Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-cone protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP:guanido phosphotransferase active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP:guanido phosphotransferase active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

RNA helicase, ATP-dependent, SK12/DOB1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the RNA helicase, ATP-dependent, SK12/DOB1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inorganic polyphosphate/ATP-NAD kinase, domain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inorganic polyphosphate/ATP-NAD kinase, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-NAD kinase-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-NAD kinase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA ligase, ATP-dependent, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA ligase, ATP-dependent, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP:guanido phosphotransferase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP:guanido phosphotransferase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA ligase, ATP-dependent Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA ligase, ATP-dependent protein domain from the InterPro Predicted Protein Domain Annotations dataset.

ATP-citrate synthase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the ATP-citrate synthase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA ligase, ATP-dependent, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA ligase, ATP-dependent, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

decreased platelet atp level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased platelet atp level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrial atp synthesis coupled electron transport Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mitochondrial atp synthesis coupled electron transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal platelet atp level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal platelet atp level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ATP synthesis Gene Set

From PANTHER Pathways

proteins participating in the ATP synthesis pathway from the PANTHER Pathways dataset.

atp Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term atp in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

ATP sensitive Potassium channels Gene Set

From Reactome Pathways

proteins participating in the ATP sensitive Potassium channels pathway from the Reactome Pathways dataset.

Formation of ATP by chemiosmotic coupling Gene Set

From Reactome Pathways

proteins participating in the Formation of ATP by chemiosmotic coupling pathway from the Reactome Pathways dataset.

Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. Gene Set

From Reactome Pathways

proteins participating in the Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. pathway from the Reactome Pathways dataset.

Erythrocyte lactate transporter defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrocyte lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose transporter type 1 deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrocyte Lactate Transporter Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Erythrocyte Lactate Transporter Defect from the curated CTD Gene-Disease Associations dataset.

Glucose Transporter Type 2 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose Transporter Type 2 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

glucose transporter type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose transporter type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serotonin transporter- pro-inflammatory bias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serotonin transporter- pro-inflammatory bias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serotonin transporter protein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serotonin transporter protein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

serotonin transporter availability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serotonin transporter availability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

norepinephrine-transporter deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease norepinephrine-transporter deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dopamine transporter availability Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dopamine transporter availability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

striatal dopamine transporter Gene Set

From GAD Gene-Disease Associations

genes associated with the disease striatal dopamine transporter in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

transporter Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term transporter in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

regulation of transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transporter activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transporter activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of sodium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of sodium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of calcium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of calcium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of cholesterol transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cholesterol transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of potassium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of potassium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of sodium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of sodium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cholesterol transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cholesterol transporter activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of calcium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of calcium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of potassium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of potassium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of sodium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of sodium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of rubidium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of rubidium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of calcium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of calcium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of rubidium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of rubidium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of potassium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of potassium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

regulation of ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of rubidium ion transmembrane transporter activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of rubidium ion transmembrane transporter activity biological process from the curated GO Biological Process Annotations dataset.

sulfur amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfur amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphate ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphate ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

formate uptake transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the formate uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

iodide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the iodide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glycine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glycine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cofactor transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cofactor transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-xylose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-xylose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

monosaccharide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the monosaccharide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-proline transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-proline transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

acetyl-coa transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the acetyl-coa transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

protein transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the protein transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

putrescine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the putrescine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

coenzyme transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the coenzyme transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

substrate-specific transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the substrate-specific transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nitrate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nitrate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

mannose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the mannose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

hexose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the hexose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity l-ornithine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity l-ornithine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucoside transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucoside transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

secondary active monocarboxylate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the secondary active monocarboxylate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

branched-chain amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the branched-chain amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

pyrimidine nucleotide-sugar transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the pyrimidine nucleotide-sugar transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity lysine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity lysine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sulfur compound transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfur compound transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-asparagine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-asparagine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sterol transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sterol transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

enterobactin transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the enterobactin transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

dipeptide transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the dipeptide transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-tyrosine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-tyrosine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-alanine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-alanine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

prostaglandin transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the prostaglandin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cysteine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cysteine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

deoxynucleotide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the deoxynucleotide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

fructose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the fructose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

alanine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the alanine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

macromolecule transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the macromolecule transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-glutamate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-glutamate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-lysine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-lysine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

protein transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the protein transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

lipoprotein transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the lipoprotein transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

short-chain fatty acid uptake transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain fatty acid uptake transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphatidylcholine transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphatidylcholine transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

quaternary ammonium group transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the quaternary ammonium group transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

c4-dicarboxylate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the c4-dicarboxylate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

amine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the amine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

copper ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the copper ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nicotinate transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nicotinate transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

oxalate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the oxalate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-histidine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-histidine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

bile acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

tetracycline transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the tetracycline transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

alcohol transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the alcohol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleotide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleotide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-glutamine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-glutamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

p-p-bond-hydrolysis-driven transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the p-p-bond-hydrolysis-driven transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

amide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the amide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-threonine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-threonine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-leucine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-leucine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucuronic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucuronic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

borate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the borate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

aromatic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the aromatic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

phospholipid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the phospholipid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

drug transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the drug transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cadmium ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cadmium ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

water transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the water transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

heme transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the heme transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

choline transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the choline transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

proton-dependent peptide secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the proton-dependent peptide secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

retinol transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the retinol transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

thyroid hormone transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the thyroid hormone transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

primary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the primary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sugar transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sugar transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

peroxisomal fatty-acyl-coa transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the peroxisomal fatty-acyl-coa transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-ascorbic acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-ascorbic acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleocytoplasmic transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleocytoplasmic transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-hydroxyproline transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-hydroxyproline transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

vitamin transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the vitamin transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

anion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the anion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium-dependent phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium-dependent phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

ferrous iron uptake transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the ferrous iron uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity basic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

basic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-ornithine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-ornithine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nickel cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nickel cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

adenine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the adenine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

methotrexate transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the methotrexate transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glycerol transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glycerol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

folic acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the folic acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

toxin transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the toxin transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

coenzyme a transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the coenzyme a transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

taurine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the taurine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

organic anion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the organic anion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

siderophore transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the siderophore transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

ceramide 1-phosphate transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the ceramide 1-phosphate transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

creatine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the creatine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nitric oxide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nitric oxide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

magnesium ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the magnesium ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

fatty-acyl-coa transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the fatty-acyl-coa transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

d-glucose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the d-glucose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

vitamin transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the vitamin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cholesterol transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cholesterol transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

carboxylic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the carboxylic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

inorganic cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the inorganic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

organic cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the organic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

organic hydroxy compound transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the organic hydroxy compound transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sulfur-containing amino acid secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfur-containing amino acid secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

neutral amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the neutral amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

inorganic diphosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the inorganic diphosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

pyruvate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the pyruvate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

copper uptake transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the copper uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

organophosphate ester transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the organophosphate ester transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

formate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the formate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleobase transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleobase transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

inorganic phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the inorganic phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sulfate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sulfate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

potassium ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the potassium ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

iron ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the iron ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

substrate-specific transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the substrate-specific transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

zinc ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the zinc ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

oligopeptide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the oligopeptide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

pyrimidine nucleobase transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the pyrimidine nucleobase transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

canalicular bile acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the canalicular bile acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

riboflavin transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the riboflavin transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium-dependent l-ascorbate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium-dependent l-ascorbate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

hexose phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the hexose phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

tricarboxylic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the tricarboxylic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

polyamine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the polyamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

neurotransmitter transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the neurotransmitter transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

thiamine uptake transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the thiamine uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

purine nucleotide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the purine nucleotide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

urate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the urate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

carbon dioxide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the carbon dioxide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

azole transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the azole transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

s-adenosyl-l-methionine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the s-adenosyl-l-methionine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

proton-dependent oligopeptide secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the proton-dependent oligopeptide secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

inorganic anion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the inorganic anion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

succinate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the succinate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

carbohydrate derivative transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the carbohydrate derivative transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

organic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the organic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

oligopeptide transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the oligopeptide transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

modified amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the modified amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

lipid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the lipid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glycolipid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glycolipid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

fad transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the fad transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-cystine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-cystine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

oxygen transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the oxygen transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

polyol transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the polyol transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrogen ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the hydrogen ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

dopamine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the dopamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

efflux transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the efflux transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

malate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the malate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cobalt ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cobalt ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sphingolipid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sphingolipid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

adenine nucleotide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the adenine nucleotide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

acidic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the acidic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

acyl carnitine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the acyl carnitine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

monocarboxylic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the monocarboxylic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

rna transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the rna transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

divalent inorganic cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the divalent inorganic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glycoprotein transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glycoprotein transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

serotonin transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the serotonin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphatidic acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphatidic acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

purine ribonucleotide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the purine ribonucleotide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-n-acetylglucosamine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-n-acetylglucosamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

lactate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the lactate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nad transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nad transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

secondary active sulfate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the secondary active sulfate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cystine secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cystine secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-serine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-serine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

metal ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the metal ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium-dependent multivitamin transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium-dependent multivitamin transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

p-p-bond-hydrolysis-driven protein transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the p-p-bond-hydrolysis-driven protein transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

fatty acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

gamma-aminobutyric acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the gamma-aminobutyric acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

dicarboxylic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the dicarboxylic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium-independent organic anion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium-independent organic anion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-galactose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-galactose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleotide-sugar transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleotide-sugar transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

secondary active organic cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the secondary active organic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-methionine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-methionine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

molybdate ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the molybdate ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

short-chain fatty acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

acetylcholine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the acetylcholine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

purine nucleobase transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the purine nucleobase transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

ferrous iron transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the ferrous iron transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

neutral l-amino acid secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the neutral l-amino acid secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

monoamine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the monoamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

transition metal ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the transition metal ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

azole transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the azole transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity glutamate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity glutamate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

salt transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the salt transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

ammonium transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the ammonium transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

bicarbonate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the bicarbonate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

mevalonate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the mevalonate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

secondary active oligopeptide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the secondary active oligopeptide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

xenobiotic transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the xenobiotic transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

fmn transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the fmn transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

amp transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the amp transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity oligopeptide transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity oligopeptide transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

carbohydrate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the carbohydrate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

adenosine 3',5'-bisphosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the adenosine 3',5'-bisphosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

serine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the serine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

icosanoid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the icosanoid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleobase-containing compound transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleobase-containing compound transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

methionine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the methionine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

nucleoside transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the nucleoside transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

manganese ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the manganese ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity l-arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity l-arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

pyrimidine nucleotide transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the pyrimidine nucleotide transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

carbohydrate transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the carbohydrate transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

thiamine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the thiamine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

uptake transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the uptake transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

antibiotic transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the antibiotic transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

3'-phosphoadenosine 5'-phosphosulfate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the 3'-phosphoadenosine 5'-phosphosulfate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

pyruvate secondary active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the pyruvate secondary active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sialic acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sialic acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

peptide transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the peptide transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

acetate ester transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the acetate ester transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

cmp-n-acetylneuraminate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the cmp-n-acetylneuraminate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

active transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the active transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

arsenite transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the arsenite transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

purine nucleoside transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the purine nucleoside transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

citrate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the citrate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

norepinephrine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the norepinephrine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

amino-acid betaine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the amino-acid betaine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

drug transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the drug transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

l-aspartate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the l-aspartate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

carnitine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the carnitine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity basic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

lead ion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the lead ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

phosphatidylinositol transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the phosphatidylinositol transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

formate efflux transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the formate efflux transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

passive transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the passive transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium-dependent organic anion transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium-dependent organic anion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

monovalent inorganic cation transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the monovalent inorganic cation transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

ceramide transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the ceramide transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

adp transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the adp transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

urea transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the urea transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

dehydroascorbic acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the dehydroascorbic acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

long-chain fatty acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the long-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

5-HTT brain serotonin transporter levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the 5-HTT brain serotonin transporter levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Na/K/Cl co-transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Na/K/Cl co-transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdate-anion transporter, animal type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdate-anion transporter, animal type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Acetyl-coenzyme A transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sugar transporter, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sugar transporter, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Large neutral amino acids transporter small subunit 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Large neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Concentrative nucleoside transporter CNT1/CNT2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Concentrative nucleoside transporter CNT1/CNT2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thiamine transporter 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thiamine transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Thiamine transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Thiamine transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Monocarboxylate transporter 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Monocarboxylate transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gastric H+/K+-transporter P-type ATPase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gastric H+/K+-transporter P-type ATPase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Organic anion transporter polypeptide OATP Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Organic anion transporter polypeptide OATP protein domain from the InterPro Predicted Protein Domain Annotations dataset.

AmpG-like permease/Acetyl-coenzyme A transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the AmpG-like permease/Acetyl-coenzyme A transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 2 (GLUT2) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 2 (GLUT2) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Heme transporter HRG Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Heme transporter HRG protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Choline transporter-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Choline transporter-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Retinal-specific ATP-binding cassette transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Retinal-specific ATP-binding cassette transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdate-anion transporter MOT2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdate-anion transporter MOT2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 3 (GLUT3) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 3 (GLUT3) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proton-dependent oligopeptide transporter family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proton-dependent oligopeptide transporter family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Citrate transporter-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Citrate transporter-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Magnesium transporter MRS2/LPE10 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Magnesium transporter MRS2/LPE10 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleotide-sugar transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleotide-sugar transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Magnesium transporter NIPA Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Magnesium transporter NIPA protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Na/K/Cl co-transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Na/K/Cl co-transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fructose transporter, type 5 (GLUT5) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fructose transporter, type 5 (GLUT5) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Monocarboxylate transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Monocarboxylate transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ammonium/urea transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ammonium/urea transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sugar phosphate transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sugar phosphate transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Amino acid/polyamine transporter I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Amino acid/polyamine transporter I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Concentrative nucleoside transporter N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Concentrative nucleoside transporter N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Equilibrative nucleoside transporter 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Equilibrative nucleoside transporter 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Equilibrative nucleoside transporter 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Equilibrative nucleoside transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Equilibrative nucleoside transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Equilibrative nucleoside transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Equilibrative nucleoside transporter 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Equilibrative nucleoside transporter 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Organic solute transporter subunit alpha/Transmembrane protein 184 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Organic solute transporter subunit alpha/Transmembrane protein 184 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Na/K/Cl co-transporter superfamily Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Na/K/Cl co-transporter superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP/CMP-sugar transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP/CMP-sugar transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

K/Cl co-transporter 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the K/Cl co-transporter 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Equilibrative nucleoside transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Equilibrative nucleoside transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Organic solute transporter subunit beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Organic solute transporter subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ctr copper transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ctr copper transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Solute carrier family 26 member 8 (testis anion transporter 1) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Solute carrier family 26 member 8 (testis anion transporter 1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphate transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphate transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Peroxysomal long chain fatty acyl transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Peroxysomal long chain fatty acyl transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

General substrate transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the General substrate transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Concentrative nucleoside transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Concentrative nucleoside transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Canalicular multispecific organic anion transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Canalicular multispecific organic anion transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Canalicular multispecific organic anion transporter 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Canalicular multispecific organic anion transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UAA transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UAA transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eukaryotic translation initiation factor 4E transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eukaryotic translation initiation factor 4E transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Concentrative nucleoside transporter C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Concentrative nucleoside transporter C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Nucleotide-sugar transporter-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nucleotide-sugar transporter-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Triose-phosphate transporter domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Triose-phosphate transporter domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cationic amino acid transporter, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cationic amino acid transporter, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Endoplasmic reticulum vesicle transporter, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Endoplasmic reticulum vesicle transporter, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 1 (GLUT1) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 1 (GLUT1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

L-type amino acid transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the L-type amino acid transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Magnesium transporter protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Magnesium transporter protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Antigen peptide transporter 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Antigen peptide transporter 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Antigen peptide transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Antigen peptide transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cobalamin (vitamin B12)-binding transporter, eukaryotic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cobalamin (vitamin B12)-binding transporter, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Folate transporter 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Folate transporter 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Amino acid transporter, transmembrane Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Amino acid transporter, transmembrane protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sulphate anion transporter, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sulphate anion transporter, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sugar/inositol transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sugar/inositol transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ammonium transporter AmtB-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ammonium transporter AmtB-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Proton-conducting membrane transporter, N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Proton-conducting membrane transporter, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cationic amino acid transporter 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cationic amino acid transporter 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oligopeptide transporter Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oligopeptide transporter protein domain from the InterPro Predicted Protein Domain Annotations dataset.