Name

ETFA Gene

electron-transfer-flavoprotein, alpha polypeptide

ETFA participates in catalyzing the initial step of the mitochondrial fatty acid beta-oxidation. It shuttles electrons between primary flavoprotein dehydrogenases and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. Defects in electron-transfer-flavoprotein have been implicated in type II glutaricaciduria in which multiple acyl-CoA dehydrogenase deficiencies result in large excretion of glutaric, lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ETFB Gene

electron-transfer-flavoprotein, beta polypeptide

This gene encodes electron-transfer-flavoprotein, beta polypeptide, which shuttles electrons between primary flavoprotein dehydrogenases involved in mitochondrial fatty acid and amino acid catabolism and the membrane-bound electron transfer flavoprotein ubiquinone oxidoreductase. The gene deficiencies have been implicated in type II glutaricaciduria. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]

ETFRF1 Gene

electron transfer flavoprotein regulatory factor 1

Involved in respiratory electron transport chain. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

ETFBKMT Gene

electron transfer flavoprotein subunit beta lysine methyltransferase

Enables heat shock protein binding activity and protein-lysine N-methyltransferase activity. Involved in negative regulation of fatty acid beta-oxidation using acyl-CoA dehydrogenase. Located in mitochondrial matrix. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025]

ETFDH Gene

electron-transferring-flavoprotein dehydrogenase

This gene encodes a component of the electron-transfer system in mitochondria and is essential for electron transfer from a number of mitochondrial flavin-containing dehydrogenases to the main respiratory chain. Mutations in this gene are associated with glutaric acidemia. Alternatively spliced transcript variants that encode distinct isoforms have been observed. [provided by RefSeq, Aug 2013]

SDHA Gene

succinate dehydrogenase complex, subunit A, flavoprotein (Fp)

This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014]

LOC220729 Gene

succinate dehydrogenase complex, subunit A, flavoprotein (Fp) pseudogene

SDHAP2 Gene

succinate dehydrogenase complex, subunit A, flavoprotein pseudogene 2

SDHAP3 Gene

succinate dehydrogenase complex, subunit A, flavoprotein pseudogene 3

SDHAP1 Gene

succinate dehydrogenase complex, subunit A, flavoprotein pseudogene 1

WWOX Gene

WW domain containing oxidoreductase

This gene encodes a member of the short-chain dehydrogenases/reductases (SDR) protein family. This gene spans the FRA16D common chromosomal fragile site and appears to function as a tumor suppressor gene. Expression of the encoded protein is able to induce apoptosis, while defects in this gene are associated with multiple types of cancer. Disruption of this gene is also associated with autosomal recessive spinocerebellar ataxia 12. Disruption of a similar gene in mouse results in impaired steroidogenesis, additionally suggesting a metabolic function for the protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]

FOXRED2 Gene

FAD-dependent oxidoreductase domain containing 2

Enables flavin adenine dinucleotide binding activity. Involved in ERAD pathway. Located in endoplasmic reticulum lumen. [provided by Alliance of Genome Resources, Mar 2025]

FOXRED1 Gene

FAD-dependent oxidoreductase domain containing 1

This gene encodes a protein that contains a FAD-dependent oxidoreductase domain. The encoded protein is localized to the mitochondria and may function as a chaperone protein required for the function of mitochondrial complex I. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2010]

MGC34796 Gene

sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase) pseudogene

NDOR1 Gene

NADPH dependent diflavin oxidoreductase 1

This gene encodes an NADPH-dependent diflavin reductase that contains both flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) binding domains. The encoded protein catalyzes the transfer of electrons from NADPH through FAD and FMN cofactors to potential redox partners. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2012]

OXNAD1 Gene

oxidoreductase NAD-binding domain containing 1

Predicted to enable oxidoreductase activity. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

NOXRED1 Gene

NADP-dependent oxidoreductase domain containing 1

Predicted to enable pyrroline-5-carboxylate reductase activity. Predicted to be involved in L-proline biosynthetic process. [provided by Alliance of Genome Resources, Mar 2025]

SPR Gene

sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)

This gene encodes an aldo-keto reductase that catalyzes the NADPH-dependent reduction of pteridine derivatives and is important in the biosynthesis of tetrahydrobiopterin (BH4). Mutations in this gene result in DOPA-responsive dystonia due to sepiaterin reductase deficiency. A pseudogene has been identified on chromosome 1. [provided by RefSeq, Jul 2008]

GFOD2 Gene

glucose-fructose oxidoreductase domain containing 2

Predicted to enable nucleotide binding activity and oxidoreductase activity. Predicted to be involved in extracellular matrix organization. Predicted to be located in extracellular region. Predicted to be active in extracellular matrix. [provided by Alliance of Genome Resources, Mar 2025]

GFOD1 Gene

glucose-fructose oxidoreductase domain containing 1

Predicted to enable nucleotide binding activity and oxidoreductase activity. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025]

LACC1 Gene

laccase (multicopper oxidoreductase) domain containing 1

This gene encodes an oxidoreductase that promotes fatty-acid oxidation, with concomitant inflammasome activation, mitochondrial and NADPH-oxidase-dependent reactive oxygen species production, and bactericidal activity of macrophages. The encoded protein forms a complex with fatty acid synthase on peroxisomes and is thought to be modulated by peroxisome proliferator-activated receptor signaling events. Naturally occurring mutations in this gene are associated with inflammatory bowel disease, Behcet's disease, leprosy, ulcerative colitis, early-onset Crohn's disease, and systemic juvenile idiopathic arthritis. [provided by RefSeq, Apr 2017]

LOC100526736 Gene

quinone oxidoreductase-like protein 2 pseudogene

LOC100421868 Gene

glucose-fructose oxidoreductase domain containing 2 pseudogene

POR Gene

P450 (cytochrome) oxidoreductase

This gene encodes an endoplasmic reticulum membrane oxidoreductase that is essential for multiple metabolic processes, including reactions catalyzed by cytochrome P450 proteins for metabolism of steroid hormones, drugs and xenobiotics. The encoded protein has a flavin adenine dinucleotide (FAD)-binding domain and a flavodoxin-like domain which bind two cofactors, FAD and FMN, that allow it to donate electrons directly from NADPH to all microsomal P450 enzymes. Mutations in this gene cause a complex set of disorders, including apparent combined P450C17 and P450C21 deficiency, amenorrhea and disordered steroidogenesis, congenital adrenal hyperplasia and Antley-Bixler syndrome, that resemble those caused by defects in steroid metabolizing enzymes such as aromatase, 21-hydroxylase, and 17 alpha-hydroxylase. [provided by RefSeq, Aug 2020]

OXLD1 Gene

oxidoreductase-like domain containing 1

Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

PYROXD2 Gene

pyridine nucleotide-disulphide oxidoreductase domain 2

Predicted to enable oxidoreductase activity. Involved in mitochondrion organization. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Mar 2025]

PYROXD1 Gene

pyridine nucleotide-disulphide oxidoreductase domain 1

This gene encodes a nuclear-cytoplasmic pyridine nucleotide-disulphide reductase (PNDR). PNDRs are flavoproteins that catalyze the pyridine nucleotide-dependent reduction of thiol residues in other proteins. The encoded protein belongs to the class I pyridine nucleotide-disulphide oxidoreductase family but lacks the C-terminal dimerization domain found in other family members and instead has a C-terminal nitrile reductase domain. It localizes to the nucleus and to striated sarcomeric compartments. Naturally occurring mutations in this gene cause early-onset myopathy with internalized nuclei and myofibrillar disorganization. A pseudogene of this gene has been defined on chromosome 11. [provided by RefSeq, Apr 2017]

LOC100422300 Gene

pyridine nucleotide-disulphide oxidoreductase domain 1 pseudogene

LOC730102 Gene

quinone oxidoreductase-like protein 2 pseudogene

ERO1B Gene

endoplasmic reticulum oxidoreductase 1 beta

Enables protein-disulfide reductase activity and thiol oxidase activity. Involved in protein folding in endoplasmic reticulum. Predicted to be located in endoplasmic reticulum. Predicted to be active in endoplasmic reticulum lumen and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025]

SQOR Gene

sulfide quinone oxidoreductase

The protein encoded by this gene may function in mitochondria to catalyze the conversion of sulfide to persulfides, thereby decreasing toxic concencrations of sulfide. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2012]

ERO1A Gene

endoplasmic reticulum oxidoreductase 1 alpha

Enables oxidoreductase activity. Involved in cell redox homeostasis and chaperone cofactor-dependent protein refolding. Located in Golgi lumen; endoplasmic reticulum; and extracellular space. [provided by Alliance of Genome Resources, Mar 2025]

TRNAK-CUU Gene

transfer RNA lysine (anticodon CUU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAA-AGC Gene

transfer RNA alanine (anticodon AGC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRL-AAG4-1 Gene

transfer RNA-Leu (AAG) 4-1

TRR-CCT5-1 Gene

transfer RNA-Arg (CCT) 5-1

TRG-CCC1-1 Gene

transfer RNA-Gly (CCC) 1-1

TRW-CCA5-1 Gene

transfer RNA-Trp (CCA) 5-1

TRG-CCC2-2 Gene

transfer RNA-Gly (CCC) 2-2

TRP-AGG1-1 Gene

transfer RNA-Pro (AGG) 1-1

TRA-AGC9-1 Gene

transfer RNA-Ala (AGC) 9-1

TRA-AGC9-2 Gene

transfer RNA-Ala (AGC) 9-2

TRK-TTT17-1 Gene

transfer RNA-Lys (TTT) 17-1

NMTRS-TGA3-1 Gene

nuclear-encoded mitochondrial transfer RNA-Ser (TGA) 3-1

TRG-CCC5-1 Gene

transfer RNA-Gly (CCC) 5-1

TRW-CCA4-1 Gene

transfer RNA-Trp (CCA) 4-1

TRK-TTT6-1 Gene

transfer RNA-Lys (TTT) 6-1

PLTP Gene

phospholipid transfer protein

The protein encoded by this gene is one of at least two lipid transfer proteins found in human plasma. The encoded protein transfers phospholipids from triglyceride-rich lipoproteins to high density lipoprotein (HDL). In addition to regulating the size of HDL particles, this protein may be involved in cholesterol metabolism. At least two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

TRC-GCA2-4 Gene

transfer RNA-Cys (GCA) 2-4

TRS-TGA3-1 Gene

transfer RNA-Ser (TGA) 3-1

TRC-GCA2-1 Gene

transfer RNA-Cys (GCA) 2-1

TRC-GCA2-2 Gene

transfer RNA-Cys (GCA) 2-2

TRC-GCA2-3 Gene

transfer RNA-Cys (GCA) 2-3

TRD-GTC6-1 Gene

transfer RNA-Asp (GTC) 6-1

TRG-TCC2-6 Gene

transfer RNA-Gly (TCC) 2-6

TRG-TCC2-5 Gene

transfer RNA-Gly (TCC) 2-5

TRG-TCC2-3 Gene

transfer RNA-Gly (TCC) 2-3

TRG-TCC2-2 Gene

transfer RNA-Gly (TCC) 2-2

TRG-TCC2-1 Gene

transfer RNA-Gly (TCC) 2-1

PITPNC1 Gene

phosphatidylinositol transfer protein, cytoplasmic 1

This gene encodes a member of the phosphatidylinositol transfer protein family. The encoded cytoplasmic protein plays a role in multiple processes including cell signaling and lipid metabolism by facilitating the transfer of phosphatidylinositol between membrane compartments. 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 1. [provided by RefSeq, May 2012]

TRNAR-ACG Gene

transfer RNA arginine (anticodon ACG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRC-GCA9-4 Gene

transfer RNA-Cys (GCA) 9-4

TRN-GTT8-1 Gene

transfer RNA-Asn (GTT) 8-1

TRL-TAG1-1 Gene

transfer RNA-Leu (TAG) 1-1

TRN-GTT17-1 Gene

transfer RNA-Asn (GTT) 17-1

NMTRL-TAA1-1 Gene

nuclear-encoded mitochondrial transfer RNA-Leu (TAA) 1-1

TRQ-CTG8-2 Gene

transfer RNA-Gln (CTG) 8-2

TRT-CGT2-1 Gene

transfer RNA-Thr (CGT) 2-1

TRK-TTT2-1 Gene

transfer RNA-Lys (TTT) 2-1

TRUND-NNN6-1 Gene

transfer RNA-undetermined (NNN) 6-1

TRQ-CTG18-1 Gene

transfer RNA-Gln (CTG) 18-1

TRG-TCC6-1 Gene

transfer RNA-Gly (TCC) 6-1

TRC-GCA11-1 Gene

transfer RNA-Cys (GCA) 11-1

TRL-AAG5-1 Gene

transfer RNA-Leu (AAG) 5-1

TRA-TGC1-1 Gene

transfer RNA-Ala (TGC) 1-1

TRQ-CTG1-5 Gene

transfer RNA-Gln (CTG) 1-5

TRV-CAC4-1 Gene

transfer RNA-Val (CAC) 4-1

TRA-AGC8-1 Gene

transfer RNA-Ala (AGC) 8-1

TRA-AGC8-2 Gene

transfer RNA-Ala (AGC) 8-2

TRF-GAA5-1 Gene

transfer RNA-Phe (GAA) 5-1

TRG-CCC1-2 Gene

transfer RNA-Gly (CCC) 1-2

TRS-TGA2-1 Gene

transfer RNA-Ser (TGA) 2-1

Hong et al. (1987) [PubMed 3648680] sequenced a human serine (UGA) tRNA by the dideoxysequencing method. The gene forms a typical cloverleaf structure with all appropriate conserved bases. It shows high nucleotide sequence homology with a previously sequenced serine tRNA (Yoo, 1984).[supplied by OMIM, Sep 2009]

TRN-GTT14-1 Gene

transfer RNA-Asn (GTT) 14-1

TRA-AGC21-1 Gene

transfer RNA-Ala (AGC) 21-1

TRK-TTT7-1 Gene

transfer RNA-Lys (TTT) 7-1

TRR-CCG1-1 Gene

transfer RNA-Arg (CCG) 1-1

TRA-TGC10-1 Gene

transfer RNA-Ala (TGC) 10-1

TRNAH-GUG Gene

transfer RNA histidine(anticodon GUG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRSUP-TTA1-1 Gene

transfer RNA suppressor (TTA) 1-1

TRL-CAG1-6 Gene

transfer RNA-Leu (CAG) 1-6

TRL-CAG1-7 Gene

transfer RNA-Leu (CAG) 1-7

TRL-CAG1-4 Gene

transfer RNA-Leu (CAG) 1-4

TRL-CAG1-5 Gene

transfer RNA-Leu (CAG) 1-5

TRL-CAG1-2 Gene

transfer RNA-Leu (CAG) 1-2

TRL-CAG1-3 Gene

transfer RNA-Leu (CAG) 1-3

TRL-CAG1-1 Gene

transfer RNA-Leu (CAG) 1-1

TRNAY-GUA Gene

transfer RNA tyrosine (anticodon GUA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRA-AGC10-1 Gene

transfer RNA-Ala (AGC) 10-1

TRT-AGT4-1 Gene

transfer RNA-Thr (AGT) 4-1

TRR-TCT1-1 Gene

transfer RNA-Arg (TCT) 1-1

TRN-GTT9-2 Gene

transfer RNA-Asn (GTT) 9-2

TRS-TGA1-1 Gene

transfer RNA-Ser (TGA) 1-1

TRQ-CTG9-1 Gene

transfer RNA-Gln (CTG) 9-1

TRR-TCT4-1 Gene

transfer RNA-Arg (TCT) 4-1

TRK-TTT3-1 Gene

transfer RNA-Lys (TTT) 3-1

TRK-TTT3-2 Gene

transfer RNA-Lys (TTT) 3-2

TRK-TTT3-3 Gene

transfer RNA-Lys (TTT) 3-3

TRK-TTT3-4 Gene

transfer RNA-Lys (TTT) 3-4

TRQ-CTG15-1 Gene

transfer RNA-Gln (CTG) 15-1

TRM-CAT2-1 Gene

transfer RNA-Met (CAT) 2-1

TRY-GTA10-1 Gene

transfer RNA-Tyr (GTA) 10-1

TRNAL-UAG Gene

transfer RNA leucine (anticodon UAG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRR-TCG1-1 Gene

transfer RNA-Arg (TCG) 1-1

TRA-AGC1-1 Gene

transfer RNA-Ala (AGC) 1-1

TRR-TCT5-1 Gene

transfer RNA-Arg (TCT) 5-1

NMTRQ-TTG8-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 8-1

TRR-CCT1-1 Gene

transfer RNA-Arg (CCT) 1-1

TRQ-CTG14-1 Gene

transfer RNA-Gln (CTG) 14-1

TRM-CAT3-2 Gene

transfer RNA-Met (CAT) 3-2

TRM-CAT3-1 Gene

transfer RNA-Met (CAT) 3-1

TRM-CAT6-1 Gene

transfer RNA-Met (CAT) 6-1

TRV-CAC5-1 Gene

transfer RNA-Val (CAC) 5-1

TRH-GTG1-7 Gene

transfer RNA-His (GTG) 1-7

TRH-GTG1-6 Gene

transfer RNA-His (GTG) 1-6

TRH-GTG1-5 Gene

transfer RNA-His (GTG) 1-5

TRH-GTG1-4 Gene

transfer RNA-His (GTG) 1-4

TRH-GTG1-1 Gene

transfer RNA-His (GTG) 1-1

TRS-CGA3-1 Gene

transfer RNA-Ser (CGA) 3-1

TRE-CTC8-1 Gene

transfer RNA-Glu (CTC) 8-1

TRNAR-UCU Gene

transfer RNA arginine (anticodon UCU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRF-GAA12-1 Gene

transfer RNA-Phe (GAA) 12-1

TRNAR-UCG Gene

transfer RNA arginine (anticodon UCG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRF-GAA8-1 Gene

transfer RNA-Phe (GAA) 8-1

TRI-TAT1-1 Gene

transfer RNA-Ile (TAT) 1-1

TRI-AAT4-1 Gene

transfer RNA-Ile (AAT) 4-1

TRE-TTC3-1 Gene

transfer RNA-Glu (TTC) 3-1

TRL-TAA1-1 Gene

transfer RNA-Leu (TAA) 1-1

TRR-ACG1-1 Gene

transfer RNA-Arg (ACG) 1-1

TRR-ACG1-2 Gene

transfer RNA-Arg (ACG) 1-2

GLTP Gene

glycolipid transfer protein

The protein encoded by this gene is similar to bovine and porcine proteins which accelerate transfer of certain glycosphingolipids and glyceroglycolipids between membranes. It is thought to be a cytoplasmic protein. [provided by RefSeq, Jul 2008]

TRK-CTT13-1 Gene

transfer RNA-Lys (CTT) 13-1

TRV-CAC1-1 Gene

transfer RNA-Val (CAC) 1-1

TRV-CAC1-2 Gene

transfer RNA-Val (CAC) 1-2

TRV-CAC1-3 Gene

transfer RNA-Val (CAC) 1-3

TRV-CAC1-5 Gene

transfer RNA-Val (CAC) 1-5

TRV-CAC1-6 Gene

transfer RNA-Val (CAC) 1-6

TRS-AGA7-1 Gene

transfer RNA-Ser (AGA) 7-1

TRE-TTC2-1 Gene

transfer RNA-Glu (TTC) 2-1

NMTRQ-TTG2-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 2-1

TRI-AAT5-2 Gene

transfer RNA-Ile (AAT) 5-2

TRI-AAT5-3 Gene

transfer RNA-Ile (AAT) 5-3

TRI-AAT5-1 Gene

transfer RNA-Ile (AAT) 5-1

TRI-AAT5-4 Gene

transfer RNA-Ile (AAT) 5-4

TRI-AAT5-5 Gene

transfer RNA-Ile (AAT) 5-5

TRNAA-CGC Gene

transfer RNA alanine (anticodon CGC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAR-CCU Gene

transfer RNA arginine (anticodon CCU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAR-CCG Gene

transfer RNA arginine (anticodon CCG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRL-CAA6-1 Gene

transfer RNA-Leu (CAA) 6-1

TRA-CGC3-1 Gene

transfer RNA-Ala (CGC) 3-1

TRY-GTA1-1 Gene

transfer RNA-Tyr (GTA) 1-1

TRE-CTC18-1 Gene

transfer RNA-Glu (CTC) 18-1

TRE-TTC16-1 Gene

transfer RNA-Glu (TTC) 16-1

TRL-TAA4-1 Gene

transfer RNA-Leu (TAA) 4-1

TRP-AGG6-1 Gene

transfer RNA-Pro (AGG) 6-1

TRL-CAA7-1 Gene

transfer RNA-Leu (CAA) 7-1

TRS-CGA2-1 Gene

transfer RNA-Ser (CGA) 2-1

TRNAE-UUC Gene

transfer RNA glutamic acid (anticodon UUC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRE-CTC9-1 Gene

transfer RNA-Glu (CTC) 9-1

TRC-GCA9-3 Gene

transfer RNA-Cys (GCA) 9-3

TRC-GCA9-2 Gene

transfer RNA-Cys (GCA) 9-2

TRC-GCA9-1 Gene

transfer RNA-Cys (GCA) 9-1

TRE-TTC12-1 Gene

transfer RNA-Glu (TTC) 12-1

TRC-GCA15-1 Gene

transfer RNA-Cys (GCA) 15-1

TRC-GCA10-1 Gene

transfer RNA-Cys (GCA) 10-1

NMTRQ-TTG3-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 3-1

TRN-GTT11-2 Gene

transfer RNA-Asn (GTT) 11-2

TRN-GTT11-1 Gene

transfer RNA-Asn (GTT) 11-1

TRC-GCA8-1 Gene

transfer RNA-Cys (GCA) 8-1

TRE-TTC13-1 Gene

transfer RNA-Glu (TTC) 13-1

TRN-GTT10-1 Gene

transfer RNA-Asn (GTT) 10-1

TRE-CTC15-1 Gene

transfer RNA-Glu (CTC) 15-1

TRT-AGT1-3 Gene

transfer RNA-Thr (AGT) 1-3

TRT-AGT1-2 Gene

transfer RNA-Thr (AGT) 1-2

TRT-AGT1-1 Gene

transfer RNA-Thr (AGT) 1-1

TRA-CGC2-1 Gene

transfer RNA-Ala (CGC) 2-1

TRT-CGT3-1 Gene

transfer RNA-Thr (CGT) 3-1

TRS-TGA4-1 Gene

transfer RNA-Ser (TGA) 4-1

Hong et al. (1992) [PubMed 1549482] sequenced a human serine tRNA by the dideoxysequencing method. Sequence analysis revealed that the gene forms a typical cloverleaf structure with all appropriate conserved bases, and that the anticodon sequence is 5-prime-UGA-3-prime. The gene has no introns and its nucleotide sequence is highly homologous to those of previously characterized serine tRNAs.[supplied by OMIM, Sep 2009]

TRUND-NNN7-1 Gene

transfer RNA-undetermined (NNN) 7-1

TRC-GCA21-1 Gene

transfer RNA-Cys (GCA) 21-1

NMTRQ-TTG12-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 12-1

TRSUP-TTA2-1 Gene

transfer RNA suppressor (TTA) 2-1

TRE-CTC14-1 Gene

transfer RNA-Glu (CTC) 14-1

TRY-ATA1-1 Gene

transfer RNA-Tyr (ATA) 1-1

TRK-CTT5-1 Gene

transfer RNA-Lys (CTT) 5-1

TRC-GCA20-1 Gene

transfer RNA-Cys (GCA) 20-1

TRG-GCC6-1 Gene

transfer RNA-Gly (GCC) 6-1

TRQ-TTG8-1 Gene

transfer RNA-Gln (TTG) 8-1

TRA-AGC2-2 Gene

transfer RNA-Ala (AGC) 2-2

TRD-GTC2-10 Gene

transfer RNA-Asp (GTC) 2-10

TRD-GTC2-11 Gene

transfer RNA-Asp (GTC) 2-11

TRA-AGC11-1 Gene

transfer RNA-Ala (AGC) 11-1

TRK-CTT4-1 Gene

transfer RNA-Lys (CTT) 4-1

TRNAY-AUA Gene

transfer RNA tyrosine (anticodon AUA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

NMTRS-TGA2-1 Gene

nuclear-encoded mitochondrial transfer RNA-Ser (TGA) 2-1

TRK-TTT8-1 Gene

transfer RNA-Lys (TTT) 8-1

TRV-AAC6-1 Gene

transfer RNA-Val (AAC) 6-1

TRS-AGA2-6 Gene

transfer RNA-Ser (AGA) 2-6

TRI-AAT8-1 Gene

transfer RNA-Ile (AAT) 8-1

TRL-TAG4-1 Gene

transfer RNA-Leu (TAG) 4-1

TRN-GTT6-1 Gene

transfer RNA-Asn (GTT) 6-1

TRV-AAC1-2 Gene

transfer RNA-Val (AAC) 1-2

TRV-AAC1-3 Gene

transfer RNA-Val (AAC) 1-3

TRT-TGT3-1 Gene

transfer RNA-Thr (TGT) 3-1

TRV-AAC2-1 Gene

transfer RNA-Val (AAC) 2-1

PCTP Gene

phosphatidylcholine transfer protein

Enables phosphatidylcholine binding activity and phosphatidylcholine transporter activity. Involved in phospholipid transport. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Mar 2025]

TRK-TTT9-1 Gene

transfer RNA-Lys (TTT) 9-1

TRG-GCC2-2 Gene

transfer RNA-Gly (GCC) 2-2

TRN-GTT7-1 Gene

transfer RNA-Asn (GTT) 7-1

NMTRQ-TTG6-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 6-1

TRN-GTT22-1 Gene

transfer RNA-Asn (GTT) 22-1

TRNAS-CGA Gene

transfer RNA serine (anticodon CGA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAV-UAC Gene

transfer RNA valine (anticodon UAC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRY-GTA5-2 Gene

transfer RNA-Tyr (GTA) 5-2

TRY-GTA5-3 Gene

transfer RNA-Tyr (GTA) 5-3

TRY-GTA5-1 Gene

transfer RNA-Tyr (GTA) 5-1

TRY-GTA5-4 Gene

transfer RNA-Tyr (GTA) 5-4

TRY-GTA5-5 Gene

transfer RNA-Tyr (GTA) 5-5

NMTRQ-TTG13-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 13-1

TRK-CTT9-1 Gene

transfer RNA-Lys (CTT) 9-1

TRP-TGG3-5 Gene

transfer RNA-Pro (TGG) 3-5

TRP-TGG3-4 Gene

transfer RNA-Pro (TGG) 3-4

TRP-TGG3-3 Gene

transfer RNA-Pro (TGG) 3-3

TRP-TGG3-2 Gene

transfer RNA-Pro (TGG) 3-2

TRP-TGG3-1 Gene

transfer RNA-Pro (TGG) 3-1

TRNAG-CCC Gene

transfer RNA glycine (anticodon CCC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAQ-UUG Gene

transfer RNA glutamine (anticodon UUG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

PITPNA Gene

phosphatidylinositol transfer protein, alpha

This gene encodes a member of a family of lipid-binding proteins that transfer molecules of phosphatidylinositol or phosphatidylcholine between membrane surfaces. The protein is implicated in phospholipase C signaling and in the production of phosphatidylinositol 3,4,5-trisphosphate (PIP3) by phosphoinositide-3-kinase.[provided by RefSeq, Sep 2009]

PITPNB Gene

phosphatidylinositol transfer protein, beta

This gene encodes a cytoplasmic protein that catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes. This transfer activity is required for COPI complex-mediated retrograde transport from the Golgi apparatus to the endoplasmic reticulum. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2013]

TRA-AGC18-1 Gene

transfer RNA-Ala (AGC) 18-1

TRA-AGC18-2 Gene

transfer RNA-Ala (AGC) 18-2

TRA-AGC3-1 Gene

transfer RNA-Ala (AGC) 3-1

NMTRV-TAC1-1 Gene

nuclear-encoded mitochondrial transfer RNA-Val (TAC) 1-1

TRC-GCA14-1 Gene

transfer RNA-Cys (GCA) 14-1

TRK-CTT8-1 Gene

transfer RNA-Lys (CTT) 8-1

TRK-TTT13-1 Gene

transfer RNA-Lys (TTT) 13-1

TRNASTOP-UUA Gene

transfer RNA ochre suppressor(anticodon UUA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

NMTRL-TAA4-1 Gene

nuclear-encoded mitochondrial transfer RNA-Leu (TAA) 4-1

TRP-TGG2-1 Gene

transfer RNA-Pro (TGG) 2-1

TRD-GTC2-6 Gene

transfer RNA-Asp (GTC) 2-6

TRD-GTC2-7 Gene

transfer RNA-Asp (GTC) 2-7

TRD-GTC2-2 Gene

transfer RNA-Asp (GTC) 2-2

TRD-GTC2-3 Gene

transfer RNA-Asp (GTC) 2-3

TRD-GTC2-8 Gene

transfer RNA-Asp (GTC) 2-8

TRV-AAC3-1 Gene

transfer RNA-Val (AAC) 3-1

TRK-TTT12-1 Gene

transfer RNA-Lys (TTT) 12-1

TRA-AGC14-1 Gene

transfer RNA-Ala (AGC) 14-1

TRA-TGC4-1 Gene

transfer RNA-Ala (TGC) 4-1

NMTRL-TAA5-1 Gene

nuclear-encoded mitochondrial transfer RNA-Leu (TAA) 5-1

TRQ-CTG4-1 Gene

transfer RNA-Gln (CTG) 4-1

TRQ-CTG4-2 Gene

transfer RNA-Gln (CTG) 4-2

TRNAM-CAU Gene

transfer RNA methionine (anticodon CAU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

NMTRQ-TTG7-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 7-1

TRNAL47P Gene

transfer RNA leucine 47 (anticodon AAG) pseudogene

TRUND-NNN2-1 Gene

transfer RNA-undetermined (NNN) 2-1

TRNAF-GAA Gene

transfer RNA phenylalanine (anticodon GAA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRL-AAG2-3 Gene

transfer RNA-Leu (AAG) 2-3

TRL-AAG2-2 Gene

transfer RNA-Leu (AAG) 2-2

TRL-AAG2-1 Gene

transfer RNA-Leu (AAG) 2-1

TRL-AAG2-4 Gene

transfer RNA-Leu (AAG) 2-4

TRA-TGC5-1 Gene

transfer RNA-Ala (TGC) 5-1

TRH-GTG1-8 Gene

transfer RNA-His (GTG) 1-8

TRI-AAT3-1 Gene

transfer RNA-Ile (AAT) 3-1

TRI-GAT1-1 Gene

transfer RNA-Ile (GAT) 1-1

TRI-GAT1-2 Gene

transfer RNA-Ile (GAT) 1-2

TRI-GAT1-3 Gene

transfer RNA-Ile (GAT) 1-3

TRUND-NNN3-1 Gene

transfer RNA-undetermined (NNN) 3-1

TRQ-CTG3-2 Gene

transfer RNA-Gln (CTG) 3-2

TRNAS-AGA Gene

transfer RNA serine (anticodon AGA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRE-TTC7-1 Gene

transfer RNA-Glu (TTC) 7-1

TRA-AGC19-1 Gene

transfer RNA-Ala (AGC) 19-1

TRL-AAG6-1 Gene

transfer RNA-Leu (AAG) 6-1

TRI-AAT12-1 Gene

transfer RNA-Ile (AAT) 12-1

TRQ-CTG1-4 Gene

transfer RNA-Gln (CTG) 1-4

TRQ-CTG1-1 Gene

transfer RNA-Gln (CTG) 1-1

TRQ-CTG1-2 Gene

transfer RNA-Gln (CTG) 1-2

TRQ-CTG1-3 Gene

transfer RNA-Gln (CTG) 1-3

TRQ-TTG3-3 Gene

transfer RNA-Gln (TTG) 3-3

TRQ-TTG3-2 Gene

transfer RNA-Gln (TTG) 3-2

TRQ-TTG3-1 Gene

transfer RNA-Gln (TTG) 3-1

TRR-CCG1-2 Gene

transfer RNA-Arg (CCG) 1-2

TRR-CCG1-3 Gene

transfer RNA-Arg (CCG) 1-3

STARD10 Gene

StAR-related lipid transfer (START) domain containing 10

Predicted to enable lipid binding activity. Predicted to be involved in lipid transport. Predicted to act upstream of or within bile acid secretion and positive regulation of peroxisome proliferator activated receptor signaling pathway. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025]

STARD13 Gene

StAR-related lipid transfer (START) domain containing 13

This gene encodes a protein which contains an N-terminal sterile alpha motif (SAM) for protein-protein interactions, followed by an ATP/GTP-binding motif, a GTPase-activating protein (GAP) domain, and a C-terminal STAR-related lipid transfer (START) domain. It may be involved in regulation of cytoskeletal reorganization, cell proliferation, and cell motility, and acts as a tumor suppressor in hepatoma cells. The gene is located in a region of chromosome 13 that is associated with loss of heterozygosity in hepatocellular carcinomas. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011]

TRR-CCT4-1 Gene

transfer RNA-Arg (CCT) 4-1

STARD9 Gene

StAR-related lipid transfer (START) domain containing 9

Enables microtubule binding activity and microtubule motor activity. Involved in spindle assembly. Located in centriole; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

GLTPD2 Gene

glycolipid transfer protein domain containing 2

Predicted to enable ceramide 1-phosphate binding activity and ceramide 1-phosphate transfer activity. Predicted to be involved in ceramide transport and intermembrane lipid transfer. Predicted to be located in cytoplasm. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Mar 2025]

STARD4 Gene

StAR-related lipid transfer (START) domain containing 4

Cholesterol homeostasis is regulated, at least in part, by sterol regulatory element (SRE)-binding proteins (e.g., SREBP1; MIM 184756) and by liver X receptors (e.g., LXRA; MIM 602423). Upon sterol depletion, LXRs are inactive and SREBPs are cleaved, after which they bind promoter SREs and activate genes involved in cholesterol biosynthesis and uptake. Sterol transport is mediated by vesicles or by soluble protein carriers, such as steroidogenic acute regulatory protein (STAR; MIM 600617). STAR is homologous to a family of proteins containing a 200- to 210-amino acid STAR-related lipid transfer (START) domain, including STARD4 (Soccio et al., 2002 [PubMed 12011452]).[supplied by OMIM, Mar 2008]

STARD5 Gene

StAR-related lipid transfer (START) domain containing 5

Proteins containing a steroidogenic acute regulatory-related lipid transfer (START) domain are often involved in the trafficking of lipids and cholesterol between diverse intracellular membranes. This gene is a member of the StarD subfamily that encodes START-related lipid transfer proteins. The protein encoded by this gene is a cholesterol transporter and is also able to bind and transport other sterol-derived molecules related to the cholesterol/bile acid biosynthetic pathways such as 25-hydroxycholesterol. Its expression is upregulated during endoplasmic reticulum (ER) stress. The protein is thought to act as a cytosolic sterol transporter that moves cholesterol between intracellular membranes such as from the cytoplasm to the ER and from the ER to the Golgi apparatus. Alternative splicing of this gene produces multiple transcript variants. [provided by RefSeq, Jan 2016]

TRNAV-CAC Gene

transfer RNA valine (anticodon CAC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRL-CAA1-1 Gene

transfer RNA-Leu (CAA) 1-1

TRL-CAA1-2 Gene

transfer RNA-Leu (CAA) 1-2

TRA-AGC15-1 Gene

transfer RNA-Ala (AGC) 15-1

TRQ-TTG2-1 Gene

transfer RNA-Gln (TTG) 2-1

TRQ-CTG5-1 Gene

transfer RNA-Gln (CTG) 5-1

TRG-GCC1-5 Gene

transfer RNA-Gly (GCC) 1-5

TRG-GCC1-1 Gene

transfer RNA-Gly (GCC) 1-1

TRG-GCC1-3 Gene

transfer RNA-Gly (GCC) 1-3

TRG-GCC1-2 Gene

transfer RNA-Gly (GCC) 1-2

TRT-TGT6-1 Gene

transfer RNA-Thr (TGT) 6-1

TRF-GAA4-1 Gene

transfer RNA-Phe (GAA) 4-1

TRSUP-TTA3-1 Gene

transfer RNA suppressor (TTA) 3-1

CETP Gene

cholesteryl ester transfer protein, plasma

The protein encoded by this gene is found in plasma, where it is involved in the transfer of cholesteryl ester from high density lipoprotein (HDL) to other lipoproteins. Defects in this gene are a cause of hyperalphalipoproteinemia 1 (HALP1). Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013]

TRA-AGC2-1 Gene

transfer RNA-Ala (AGC) 2-1

TRR-TCG5-1 Gene

transfer RNA-Arg (TCG) 5-1

TRK-CTT3-1 Gene

transfer RNA-Lys (CTT) 3-1

TRG-TCC2-4 Gene

transfer RNA-Gly (TCC) 2-4

TRR-CCT7-1 Gene

transfer RNA-Arg (CCT) 7-1

TRT-TGT2-1 Gene

transfer RNA-Thr (TGT) 2-1

TRP-AGG4-1 Gene

transfer RNA-Pro (AGG) 4-1

TRS-AGA3-1 Gene

transfer RNA-Ser (AGA) 3-1

TRS-AGA2-1 Gene

transfer RNA-Ser (AGA) 2-1

TRR-TCG4-1 Gene

transfer RNA-Arg (TCG) 4-1

TRE-CTC4-1 Gene

transfer RNA-Glu (CTC) 4-1

TRN-GTT16-1 Gene

transfer RNA-Asn (GTT) 16-1

TRN-GTT16-3 Gene

transfer RNA-Asn (GTT) 16-3

TRN-GTT16-2 Gene

transfer RNA-Asn (GTT) 16-2

TRN-GTT16-5 Gene

transfer RNA-Asn (GTT) 16-5

TRN-GTT16-4 Gene

transfer RNA-Asn (GTT) 16-4

TRC-GCA1-1 Gene

transfer RNA-Cys (GCA) 1-1

TRP-AGG5-1 Gene

transfer RNA-Pro (AGG) 5-1

TRK-CTT14-1 Gene

transfer RNA-Lys (CTT) 14-1

TRV-CAC13-1 Gene

transfer RNA-Val (CAC) 13-1

TRUND-NNN1-1 Gene

transfer RNA-undetermined (NNN) 1-1

TRS-AGA2-4 Gene

transfer RNA-Ser (AGA) 2-4

Hoe et al. (1987) [PubMed 3697066] sequenced a human serine (AGA) tRNA by the dideoxysequencing method and compared it with previously sequenced serine tRNAs.[supplied by OMIM, Sep 2009]

TRS-AGA2-5 Gene

transfer RNA-Ser (AGA) 2-5

TRS-AGA2-2 Gene

transfer RNA-Ser (AGA) 2-2

TRS-AGA2-3 Gene

transfer RNA-Ser (AGA) 2-3

TRS-GCT1-1 Gene

transfer RNA-Ser (GCT) 1-1

TRL-CAA3-1 Gene

transfer RNA-Leu (CAA) 3-1

TRNAI-UAU Gene

transfer RNA isoleucine (anticodon UAU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

CPTP Gene

ceramide-1-phosphate transfer protein

Enables ceramide 1-phosphate binding activity and ceramide 1-phosphate transfer activity. Involved in ceramide 1-phosphate transport; negative regulation of NLRP3 inflammasome complex assembly; and negative regulation of metabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025]

TRE-TTC6-1 Gene

transfer RNA-Glu (TTC) 6-1

TRA-CGC1-1 Gene

transfer RNA-Ala (CGC) 1-1

TRX-CAT3-1 Gene

transfer RNA-iMet (CAT) 3-1

TRV-CAC10-1 Gene

transfer RNA-Val (CAC) 10-1

TRG-TCC3-1 Gene

transfer RNA-Gly (TCC) 3-1

TRI-AAT6-1 Gene

transfer RNA-Ile (AAT) 6-1

TRE-CTC1-7 Gene

transfer RNA-Glu (CTC) 1-7

TRE-CTC1-1 Gene

transfer RNA-Glu (CTC) 1-1

TRE-CTC1-2 Gene

transfer RNA-Glu (CTC) 1-2

TRY-GTA2-1 Gene

transfer RNA-Tyr (GTA) 2-1

TRK-CTT2-1 Gene

transfer RNA-Lys (CTT) 2-1

TRK-CTT2-2 Gene

transfer RNA-Lys (CTT) 2-2

TRK-CTT2-3 Gene

transfer RNA-Lys (CTT) 2-3

TRK-CTT2-5 Gene

transfer RNA-Lys (CTT) 2-5

TRA-AGC23-1 Gene

transfer RNA-Ala (AGC) 23-1

TRP-AGG2-3 Gene

transfer RNA-Pro (AGG) 2-3

TRP-AGG2-8 Gene

transfer RNA-Pro (AGG) 2-8

TRL-CAA4-1 Gene

transfer RNA-Leu (CAA) 4-1

TRG-GCC1-4 Gene

transfer RNA-Gly (GCC) 1-4

TRA-TGC8-1 Gene

transfer RNA-Ala (TGC) 8-1

TRW-CCA7-1 Gene

transfer RNA-Trp (CCA) 7-1

TRD-GTC9-1 Gene

transfer RNA-Asp (GTC) 9-1

TRV-CAC12-1 Gene

transfer RNA-Val (CAC) 12-1

TRU-TCA1-1 Gene

transfer RNA-SeC (TCA) 1-1

Opal suppressor phosphoserine tRNAs are the only authentic, naturally occurring suppressor tRNAs in higher eukaryotes. The human genome contains a single opal suppressor phosphoserine tRNA gene, TRNAU1 (O'Neill et al., 1985 [PubMed 3156131]).[supplied by OMIM, Nov 2010]

TRN-ATT1-2 Gene

transfer RNA-Asn (ATT) 1-2

NMTRS-TGA1-1 Gene

nuclear-encoded mitochondrial transfer RNA-Ser (TGA) 1-1

LOC100422076 Gene

phosphatidylinositol transfer protein, cytoplasmic 1 pseudogene

TRI-AAT7-1 Gene

transfer RNA-Ile (AAT) 7-1

TRI-AAT7-2 Gene

transfer RNA-Ile (AAT) 7-2

TRNAA-UGC Gene

transfer RNA alanine (anticodon UGC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRR-TCG2-1 Gene

transfer RNA-Arg (TCG) 2-1

TRC-GCA4-1 Gene

transfer RNA-Cys (GCA) 4-1

TRT-CGT1-1 Gene

transfer RNA-Thr (CGT) 1-1

TRD-GTC8-1 Gene

transfer RNA-Asp (GTC) 8-1

TRN-GTT20-1 Gene

transfer RNA-Asn (GTT) 20-1

TRX-CAT2-1 Gene

transfer RNA-iMet (CAT) 2-1

Santos and Zasloff (1981) [PubMed 6261953] identified 12 initiator methionine tRNA genes, symbolized tRNA-i(met), in the haploid human genome. Zasloff et al. (1982) [PubMed 6923137] found a variant tRNA-i(met) with a G-to-T transversion in the highly conserved TCGA sequence in loop 4, a sequence position occupied exclusively by a purine (usually G) in almost 200 prokaryotic and eukaryotic tRNAs. One functional consequence of this base substitution is reduction in the rate of processing of the primary transcript of the gene. A second, demonstrated by microinjection into the germinal vesicle of the intact Xenopus laevis oocyte, is blockage of egress from the nucleus. It has been estimated that the human haploid genome contains 1,000 to 2,000 tRNA genes and that there are 50 to 60 chromatographically distinct tRNA species. These observations suggest redundancy of some tRNA genes. The studies of initiator methionine tRNA genes bear out this suspicion.[supplied by OMIM, Sep 2009]

TRUND-NNN10-1 Gene

transfer RNA-undetermined (NNN) 10-1

TRL-TAG3-1 Gene

transfer RNA-Leu (TAG) 3-1

TRF-GAA10-1 Gene

transfer RNA-Phe (GAA) 10-1

TRUND-NNN5-1 Gene

transfer RNA-undetermined (NNN) 5-1

TRA-AGC4-1 Gene

transfer RNA-Ala (AGC) 4-1

NMTRQ-TTG11-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 11-1

TRG-CCC4-1 Gene

transfer RNA-Gly (CCC) 4-1

TRUND-NNN4-1 Gene

transfer RNA-undetermined (NNN) 4-1

TRC-GCA5-1 Gene

transfer RNA-Cys (GCA) 5-1

TRN-GTT21-1 Gene

transfer RNA-Asn (GTT) 21-1

TRS-GCT4-1 Gene

transfer RNA-Ser (GCT) 4-1

TRS-GCT4-3 Gene

transfer RNA-Ser (GCT) 4-3

TRS-GCT4-2 Gene

transfer RNA-Ser (GCT) 4-2

TTPAL Gene

tocopherol (alpha) transfer protein-like

Predicted to enable phosphatidylinositol bisphosphate binding activity. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

TRN-ATT1-1 Gene

transfer RNA-Asn (ATT) 1-1

TRL-AAG3-1 Gene

transfer RNA-Leu (AAG) 3-1

TRT-TGT4-1 Gene

transfer RNA-Thr (TGT) 4-1

TRP-AGG3-1 Gene

transfer RNA-Pro (AGG) 3-1

TRL-CAA5-1 Gene

transfer RNA-Leu (CAA) 5-1

TRA-AGC7-1 Gene

transfer RNA-Ala (AGC) 7-1

TRF-GAA6-1 Gene

transfer RNA-Phe (GAA) 6-1

TRG-CCC6-1 Gene

transfer RNA-Gly (CCC) 6-1

TRC-GCA23-1 Gene

transfer RNA-Cys (GCA) 23-1

TRK-CTT12-1 Gene

transfer RNA-Lys (CTT) 12-1

TRW-CCA6-1 Gene

transfer RNA-Trp (CCA) 6-1

TRG-GCC5-1 Gene

transfer RNA-Gly (GCC) 5-1

TRA-AGC6-1 Gene

transfer RNA-Ala (AGC) 6-1

TRL-CAG2-1 Gene

transfer RNA-Leu (CAG) 2-1

TRL-CAG2-2 Gene

transfer RNA-Leu (CAG) 2-2

TRR-ACG2-4 Gene

transfer RNA-Arg (ACG) 2-4

TRR-ACG2-3 Gene

transfer RNA-Arg (ACG) 2-3

TRR-ACG2-2 Gene

transfer RNA-Arg (ACG) 2-2

TRR-ACG2-1 Gene

transfer RNA-Arg (ACG) 2-1

TRF-GAA2-1 Gene

transfer RNA-Phe (GAA) 2-1

NMTRL-TAA3-1 Gene

nuclear-encoded mitochondrial transfer RNA-Leu (TAA) 3-1

TRK-TTT1-1 Gene

transfer RNA-Lys (TTT) 1-1

TRG-TCC1-1 Gene

transfer RNA-Gly (TCC) 1-1

TRA-TGC3-1 Gene

transfer RNA-Ala (TGC) 3-1

TRA-TGC3-2 Gene

transfer RNA-Ala (TGC) 3-2

TRL-TAG2-1 Gene

transfer RNA-Leu (TAG) 2-1

TRN-GTT2-6 Gene

transfer RNA-Asn (GTT) 2-6

TRN-GTT2-5 Gene

transfer RNA-Asn (GTT) 2-5

TRN-GTT2-4 Gene

transfer RNA-Asn (GTT) 2-4

TRN-GTT2-3 Gene

transfer RNA-Asn (GTT) 2-3

TRN-GTT2-2 Gene

transfer RNA-Asn (GTT) 2-2

TRN-GTT2-1 Gene

transfer RNA-Asn (GTT) 2-1

The saturation hybridization studies of Hatlen and Attardi (1971) [PubMed 4929578] indicated a copy number of tRNA genes of 1,300 for the haploid human genome--an average of 65 gene copies for each tRNA species. These genes tend to be clustered, an arrangement that would facilitate the exchange of sequence information and enable them to evolve together.[supplied by OMIM, Sep 2009]

NMTRQ-TTG10-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 10-1

TRE-CTC1-4 Gene

transfer RNA-Glu (CTC) 1-4

TRE-CTC1-6 Gene

transfer RNA-Glu (CTC) 1-6

TRQ-CTG17-1 Gene

transfer RNA-Gln (CTG) 17-1

TRP-AGG2-5 Gene

transfer RNA-Pro (AGG) 2-5

TRG-TCC5-1 Gene

transfer RNA-Gly (TCC) 5-1

TRS-GCT5-1 Gene

transfer RNA-Ser (GCT) 5-1

TRY-GTA12-1 Gene

transfer RNA-Tyr (GTA) 12-1

TRR-TCG3-1 Gene

transfer RNA-Arg (TCG) 3-1

TRN-GTT3-2 Gene

transfer RNA-Asn (GTT) 3-2

TRN-GTT3-1 Gene

transfer RNA-Asn (GTT) 3-1

TRF-GAA11-1 Gene

transfer RNA-Phe (GAA) 11-1

TRK-CTT2-4 Gene

transfer RNA-Lys (CTT) 2-4

TRF-GAA7-1 Gene

transfer RNA-Phe (GAA) 7-1

TRNAE-CUC Gene

transfer RNA glutamic acid (anticodon CUC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRC-GCA22-1 Gene

transfer RNA-Cys (GCA) 22-1

TRD-GTC10-1 Gene

transfer RNA-Asp (GTC) 10-1

TRM-CAT4-1 Gene

transfer RNA-Met (CAT) 4-1

TRM-CAT4-3 Gene

transfer RNA-Met (CAT) 4-3

TRM-CAT4-2 Gene

transfer RNA-Met (CAT) 4-2

TRV-CAC3-1 Gene

transfer RNA-Val (CAC) 3-1

TRH-GTG3-1 Gene

transfer RNA-His (GTG) 3-1

TRG-GCC4-1 Gene

transfer RNA-Gly (GCC) 4-1

TRV-CAC14-1 Gene

transfer RNA-Val (CAC) 14-1

TRNAI-GAU Gene

transfer RNA isoleucine (anticodon GAU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRL-CAG3-1 Gene

transfer RNA-Leu (CAG) 3-1

TRE-TTC1-1 Gene

transfer RNA-Glu (TTC) 1-1

TRE-TTC1-2 Gene

transfer RNA-Glu (TTC) 1-2

TRF-GAA3-1 Gene

transfer RNA-Phe (GAA) 3-1

NMTRQ-TTG9-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 9-1

TRK-CTT15-1 Gene

transfer RNA-Lys (CTT) 15-1

TRP-CGG1-1 Gene

transfer RNA-Pro (CGG) 1-1

TRP-CGG1-2 Gene

transfer RNA-Pro (CGG) 1-2

TRP-CGG1-3 Gene

transfer RNA-Pro (CGG) 1-3

TRNASTOP-UCA Gene

transfer RNA opal suppressor (anticodon UCA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRN-GTT9-1 Gene

transfer RNA-Asn (GTT) 9-1

TTPA Gene

tocopherol (alpha) transfer protein

This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa. [provided by RefSeq, Nov 2009]

TRA-AGC17-1 Gene

transfer RNA-Ala (AGC) 17-1

TRSUP-CTA3-1 Gene

transfer RNA suppressor (CTA) 3-1

TRA-AGC5-1 Gene

transfer RNA-Ala (AGC) 5-1

TRW-CCA3-3 Gene

transfer RNA-Trp (CCA) 3-3

TRW-CCA3-2 Gene

transfer RNA-Trp (CCA) 3-2

TRNAC-GCA Gene

transfer RNA cysteine (anticodon GCA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAP-CGG Gene

transfer RNA proline (anticodon CGG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRW-CCA1-1 Gene

transfer RNA-Trp (CCA) 1-1

TRD-GTC5-1 Gene

transfer RNA-Asp (GTC) 5-1

TRQ-CTG16-1 Gene

transfer RNA-Gln (CTG) 16-1

TRM-CAT1-1 Gene

transfer RNA-Met (CAT) 1-1

TRSUP-CTA2-1 Gene

transfer RNA suppressor (CTA) 2-1

TRA-AGC12-3 Gene

transfer RNA-Ala (AGC) 12-3

TRS-AGA5-1 Gene

transfer RNA-Ser (AGA) 5-1

TRV-TAC3-1 Gene

transfer RNA-Val (TAC) 3-1

TRK-TTT10-1 Gene

transfer RNA-Lys (TTT) 10-1

NMTRL-TAA6-1 Gene

nuclear-encoded mitochondrial transfer RNA-Leu (TAA) 6-1

TRT-CGT5-1 Gene

transfer RNA-Thr (CGT) 5-1

TRA-AGC22-1 Gene

transfer RNA-Ala (AGC) 22-1

TRP-AGG2-1 Gene

transfer RNA-Pro (AGG) 2-1

TRP-AGG2-2 Gene

transfer RNA-Pro (AGG) 2-2

TRP-AGG2-4 Gene

transfer RNA-Pro (AGG) 2-4

TRP-AGG2-7 Gene

transfer RNA-Pro (AGG) 2-7

TRM-CAT5-1 Gene

transfer RNA-Met (CAT) 5-1

TRK-TTT3-5 Gene

transfer RNA-Lys (TTT) 3-5

TRH-GTG2-1 Gene

transfer RNA-His (GTG) 2-1

TRC-GCA16-1 Gene

transfer RNA-Cys (GCA) 16-1

TRS-CGA4-1 Gene

transfer RNA-Ser (CGA) 4-1

TRA-TGC6-1 Gene

transfer RNA-Ala (TGC) 6-1

TRG-CCC3-1 Gene

transfer RNA-Gly (CCC) 3-1

TRH-GTG1-3 Gene

transfer RNA-His (GTG) 1-3

TRT-CGT6-1 Gene

transfer RNA-Thr (CGT) 6-1

TRE-TTC10-1 Gene

transfer RNA-Glu (TTC) 10-1

TRL-TAA3-1 Gene

transfer RNA-Leu (TAA) 3-1

TRL-AAG7-1 Gene

transfer RNA-Leu (AAG) 7-1

TRNAD-GUC Gene

transfer RNA aspartic acid (anticodon GUC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRC-GCA12-1 Gene

transfer RNA-Cys (GCA) 12-1

TRC-GCA6-1 Gene

transfer RNA-Cys (GCA) 6-1

TRI-AAT11-1 Gene

transfer RNA-Ile (AAT) 11-1

TRR-CCT9-1 Gene

transfer RNA-Arg (CCT) 9-1

TRG-CCC2-1 Gene

transfer RNA-Gly (CCC) 2-1

TRN-GTT13-1 Gene

transfer RNA-Asn (GTT) 13-1

TRNAL-CAG Gene

transfer RNA leucine (anticodon CAG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAL-CAA Gene

transfer RNA leucine (anticodon CAA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRG-CCC7-1 Gene

transfer RNA-Gly (CCC) 7-1

TRQ-TTG7-1 Gene

transfer RNA-Gln (TTG) 7-1

TRW-CCA2-1 Gene

transfer RNA-Trp (CCA) 2-1

TRK-TTT4-1 Gene

transfer RNA-Lys (TTT) 4-1

TRR-CCG2-1 Gene

transfer RNA-Arg (CCG) 2-1

TRR-CCT8-1 Gene

transfer RNA-Arg (CCT) 8-1

TRE-CTC17-1 Gene

transfer RNA-Glu (CTC) 17-1

TRT-AGT3-1 Gene

transfer RNA-Thr (AGT) 3-1

TRA-CGC4-1 Gene

transfer RNA-Ala (CGC) 4-1

TRQ-TTG6-1 Gene

transfer RNA-Gln (TTG) 6-1

TRK-TTT5-1 Gene

transfer RNA-Lys (TTT) 5-1

TRT-CGT4-1 Gene

transfer RNA-Thr (CGT) 4-1

TRNAG-UCC Gene

transfer RNA glycine (anticodon UCC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

NMTRP-TGG1-1 Gene

nuclear-encoded mitochondrial transfer RNA-Pro (TGG) 1-1

TRL-AAG8-1 Gene

transfer RNA-Leu (AAG) 8-1

TRNAQ-CUG Gene

transfer RNA glutamine (anticodon CUG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRA-TGC7-1 Gene

transfer RNA-Ala (TGC) 7-1

MTTP Gene

microsomal triglyceride transfer protein

MTP encodes the large subunit of the heterodimeric microsomal triglyceride transfer protein. Protein disulfide isomerase (PDI) completes the heterodimeric microsomal triglyceride transfer protein, which has been shown to play a central role in lipoprotein assembly. Mutations in MTP can cause abetalipoproteinemia. [provided by RefSeq, Jul 2008]

TRK-CTT7-1 Gene

transfer RNA-Lys (CTT) 7-1

TRR-TCT2-1 Gene

transfer RNA-Arg (TCT) 2-1

Transfer RNA arginine-1 has an anticodon UCU (Morrison et al., 1991 [PubMed 2066114]).[supplied by OMIM, Sep 2009]

TRT-AGT5-1 Gene

transfer RNA-Thr (AGT) 5-1

TRQ-CTG13-1 Gene

transfer RNA-Gln (CTG) 13-1

TRV-CAC6-1 Gene

transfer RNA-Val (CAC) 6-1

TRQ-CTG11-1 Gene

transfer RNA-Gln (CTG) 11-1

TRNAG-GCC Gene

transfer RNA glycine (anticodon GCC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRA-AGC13-2 Gene

transfer RNA-Ala (AGC) 13-2

TRI-AAT10-1 Gene

transfer RNA-Ile (AAT) 10-1

TRN-GTT12-1 Gene

transfer RNA-Asn (GTT) 12-1

TRQ-CTG10-1 Gene

transfer RNA-Gln (CTG) 10-1

TRV-CAC7-1 Gene

transfer RNA-Val (CAC) 7-1

TRK-CTT10-1 Gene

transfer RNA-Lys (CTT) 10-1

TRI-AAT2-1 Gene

transfer RNA-Ile (AAT) 2-1

TRV-CAC2-1 Gene

transfer RNA-Val (CAC) 2-1

TRS-AGA6-1 Gene

transfer RNA-Ser (AGA) 6-1

TRNAP-UGG Gene

transfer RNA proline (anticodon UGG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRE-TTC5-1 Gene

transfer RNA-Glu (TTC) 5-1

TRN-GTT4-1 Gene

transfer RNA-Asn (GTT) 4-1

TRE-CTC16-1 Gene

transfer RNA-Glu (CTC) 16-1

TRT-AGT2-2 Gene

transfer RNA-Thr (AGT) 2-2

TRK-CTT11-1 Gene

transfer RNA-Lys (CTT) 11-1

TRNAS-UGA Gene

transfer RNA serine (anticodon UGA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAT-AGU Gene

transfer RNA threonine (anticodon AGU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRV-TAC4-1 Gene

transfer RNA-Val (TAC) 4-1

TRL-TAA2-1 Gene

transfer RNA-Leu (TAA) 2-1

TRNAL-UAA Gene

transfer RNA leucine (anticodon UAA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRY-GTA6-1 Gene

transfer RNA-Tyr (GTA) 6-1

TRI-AAT9-1 Gene

transfer RNA-Ile (AAT) 9-1

TRK-CTT6-1 Gene

transfer RNA-Lys (CTT) 6-1

TRT-AGT6-1 Gene

transfer RNA-Thr (AGT) 6-1

TRR-TCT3-1 Gene

transfer RNA-Arg (TCT) 3-1

TRR-TCT3-2 Gene

transfer RNA-Arg (TCT) 3-2

TRV-AAC1-1 Gene

transfer RNA-Val (AAC) 1-1

TRS-AGA1-1 Gene

transfer RNA-Ser (AGA) 1-1

TRQ-CTG12-1 Gene

transfer RNA-Gln (CTG) 12-1

TRV-CAC8-1 Gene

transfer RNA-Val (CAC) 8-1

TRH-GTG1-9 Gene

transfer RNA-His (GTG) 1-9

TRH-GTG1-2 Gene

transfer RNA-His (GTG) 1-2

TRQ-CTG8-1 Gene

transfer RNA-Gln (CTG) 8-1

TRF-GAA9-1 Gene

transfer RNA-Phe (GAA) 9-1

TRR-TCG6-1 Gene

transfer RNA-Arg (TCG) 6-1

TRI-TAT3-1 Gene

transfer RNA-Ile (TAT) 3-1

TRV-CAC11-2 Gene

transfer RNA-Val (CAC) 11-2

TRP-GGG1-1 Gene

transfer RNA-Pro (GGG) 1-1

TRV-AAC1-4 Gene

transfer RNA-Val (AAC) 1-4

There appear to be about 1,300 tRNA genes in the human genome (Hatlen and Attardi, 1971 [PubMed 4929578]). Arnold et al. (1986) [PubMed 3023191] detected a minimum of 13 valine tRNA genes in genomic blots of human DNA.[supplied by OMIM, Sep 2009]

TRV-AAC1-5 Gene

transfer RNA-Val (AAC) 1-5

NMTRL-TAA2-1 Gene

nuclear-encoded mitochondrial transfer RNA-Leu (TAA) 2-1

TRK-TTT11-1 Gene

transfer RNA-Lys (TTT) 11-1

TRI-TAT2-2 Gene

transfer RNA-Ile (TAT) 2-2

TRI-TAT2-3 Gene

transfer RNA-Ile (TAT) 2-3

TRI-TAT2-1 Gene

transfer RNA-Ile (TAT) 2-1

TRR Gene

transfer RNA arginine

TRE-TTC4-1 Gene

transfer RNA-Glu (TTC) 4-1

TRE-TTC4-2 Gene

transfer RNA-Glu (TTC) 4-2

TRC-GCA7-1 Gene

transfer RNA-Cys (GCA) 7-1

TRP-TGG5-1 Gene

transfer RNA-Pro (TGG) 5-1

TRD-GTC4-1 Gene

transfer RNA-Asp (GTC) 4-1

TRE-TTC14-1 Gene

transfer RNA-Glu (TTC) 14-1

TRE-CTC5-1 Gene

transfer RNA-Glu (CTC) 5-1

NMTRQ-TTG1-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 1-1

NMTRQ-TTG15-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 15-1

TRV-AAC7-1 Gene

transfer RNA-Val (AAC) 7-1

TRY-GTA7-1 Gene

transfer RNA-Tyr (GTA) 7-1

TRN-GTT19-1 Gene

transfer RNA-Asn (GTT) 19-1

TRV-CAC9-1 Gene

transfer RNA-Val (CAC) 9-1

TRG-GCC2-3 Gene

transfer RNA-Gly (GCC) 2-3

TRG-GCC2-1 Gene

transfer RNA-Gly (GCC) 2-1

TRA-AGC16-1 Gene

transfer RNA-Ala (AGC) 16-1

TRE-CTC13-1 Gene

transfer RNA-Glu (CTC) 13-1

TRA-CGC5-1 Gene

transfer RNA-Ala (CGC) 5-1

TRE-CTC11-1 Gene

transfer RNA-Glu (CTC) 11-1

TRL-TAA5-1 Gene

transfer RNA-Leu (TAA) 5-1

TRV-TAC1-1 Gene

transfer RNA-Val (TAC) 1-1

TRV-TAC1-2 Gene

transfer RNA-Val (TAC) 1-2

TRA-AGC12-2 Gene

transfer RNA-Ala (AGC) 12-2

TRA-AGC12-1 Gene

transfer RNA-Ala (AGC) 12-1

TRQ-CTG7-1 Gene

transfer RNA-Gln (CTG) 7-1

TRE-CTC10-1 Gene

transfer RNA-Glu (CTC) 10-1

TRQ-TTG1-1 Gene

transfer RNA-Gln (TTG) 1-1

Mammalian cells contain at least 2 species of glutamine tRNA, the Gln(CUG) form (TRQ1; MIM 189919) and the Gln(UUG) form. Nemoto et al. (1991) [PubMed 2041751] reported the nucleotide sequence of the human tRNA(Gln/UUG) gene. In a correction, Nemoto et al. (1991) [PubMed 2041751] stated that the gene involved should have been designated tRNA-GLN/U*UG, where U* is a derivative of U.[supplied by OMIM, Sep 2009]

TRP-TGG4-1 Gene

transfer RNA-Pro (TGG) 4-1

TRE-TTC15-1 Gene

transfer RNA-Glu (TTC) 15-1

TRR-CCT3-1 Gene

transfer RNA-Arg (CCT) 3-1

TRV-TAC2-1 Gene

transfer RNA-Val (TAC) 2-1

TRS-ACT1-1 Gene

transfer RNA-Ser (ACT) 1-1

TRA-AGC13-1 Gene

transfer RNA-Ala (AGC) 13-1

PITPNM1 Gene

phosphatidylinositol transfer protein, membrane-associated 1

PITPNM1 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]

PITPNM2 Gene

phosphatidylinositol transfer protein, membrane-associated 2

PITPNM2 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]

NMTRQ-TTG14-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 14-1

TRA-TGC2-1 Gene

transfer RNA-Ala (TGC) 2-1

TRT-AGT2-1 Gene

transfer RNA-Thr (AGT) 2-1

TRL-AAG1-1 Gene

transfer RNA-Leu (AAG) 1-1

TRL-AAG1-2 Gene

transfer RNA-Leu (AAG) 1-2

TRL-AAG1-3 Gene

transfer RNA-Leu (AAG) 1-3

TRV-CAC1-4 Gene

transfer RNA-Val (CAC) 1-4

TRC-GCA18-1 Gene

transfer RNA-Cys (GCA) 18-1

TRE-CTC12-1 Gene

transfer RNA-Glu (CTC) 12-1

TRP-AGG2-6 Gene

transfer RNA-Pro (AGG) 2-6

TRC-GCA19-1 Gene

transfer RNA-Cys (GCA) 19-1

TRN-GTT18-1 Gene

transfer RNA-Asn (GTT) 18-1

TRD-GTC2-4 Gene

transfer RNA-Asp (GTC) 2-4

TRD-GTC2-5 Gene

transfer RNA-Asp (GTC) 2-5

TRY-GTA11-1 Gene

transfer RNA-Tyr (GTA) 11-1

TRY-GTA3-1 Gene

transfer RNA-Tyr (GTA) 3-1

TRD-GTC2-1 Gene

transfer RNA-Asp (GTC) 2-1

TRG-CCC8-1 Gene

transfer RNA-Gly (CCC) 8-1

TRE-TTC2-2 Gene

transfer RNA-Glu (TTC) 2-2

TRC-GCA17-1 Gene

transfer RNA-Cys (GCA) 17-1

TRNAT-CGU Gene

transfer RNA threonine (anticodon CGU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRK-CTT16-1 Gene

transfer RNA-Lys (CTT) 16-1

TRV-AAC4-1 Gene

transfer RNA-Val (AAC) 4-1

TRR-CCT2-1 Gene

transfer RNA-Arg (CCT) 2-1

TRUND-NNN9-1 Gene

transfer RNA-undetermined (NNN) 9-1

TRR-ACG1-3 Gene

transfer RNA-Arg (ACG) 1-3

TRD-GTC1-1 Gene

transfer RNA-Asp (GTC) 1-1

TRT-AGT7-1 Gene

transfer RNA-Thr (AGT) 7-1

TRT-TGT5-1 Gene

transfer RNA-Thr (TGT) 5-1

TRV-AAC5-1 Gene

transfer RNA-Val (AAC) 5-1

TRU-TCA2-1 Gene

transfer RNA-SeC (TCA) 2-1

TRG-TCC4-1 Gene

transfer RNA-Gly (TCC) 4-1

TRK-TTT15-1 Gene

transfer RNA-Lys (TTT) 15-1

TRE-CTC7-1 Gene

transfer RNA-Glu (CTC) 7-1

TRS-CGA1-1 Gene

transfer RNA-Ser (CGA) 1-1

TRN-GTT1-1 Gene

transfer RNA-Asn (GTT) 1-1

TRP-TGG1-1 Gene

transfer RNA-Pro (TGG) 1-1

TRU-TCA3-1 Gene

transfer RNA-SeC (TCA) 3-1

TRD-GTC3-1 Gene

transfer RNA-Asp (GTC) 3-1

TRD-GTC2-9 Gene

transfer RNA-Asp (GTC) 2-9

TRT-TGT1-1 Gene

transfer RNA-Thr (TGT) 1-1

TRK-TTT16-1 Gene

transfer RNA-Lys (TTT) 16-1

TRM-CAT7-1 Gene

transfer RNA-Met (CAT) 7-1

TRC-ACA1-1 Gene

transfer RNA-Cys (ACA) 1-1

TRY-GTA4-1 Gene

transfer RNA-Tyr (GTA) 4-1

TRI-AAT1-1 Gene

transfer RNA-Ile (AAT) 1-1

TRA-TGC9-1 Gene

transfer RNA-Ala (TGC) 9-1

TRE-TTC11-1 Gene

transfer RNA-Glu (TTC) 11-1

TRQ-CTG2-1 Gene

transfer RNA-Gln (CTG) 2-1

TRW-CCA3-1 Gene

transfer RNA-Trp (CCA) 3-1

TRL-CAA2-1 Gene

transfer RNA-Leu (CAA) 2-1

TRK-TTT14-1 Gene

transfer RNA-Lys (TTT) 14-1

TRQ-CTG3-1 Gene

transfer RNA-Gln (CTG) 3-1

TRQ-TTG5-1 Gene

transfer RNA-Gln (TTG) 5-1

TRY-GTA8-1 Gene

transfer RNA-Tyr (GTA) 8-1

TRQ-CTG6-1 Gene

transfer RNA-Gln (CTG) 6-1

STARD8 Gene

StAR-related lipid transfer (START) domain containing 8

This gene encodes a member of a subfamily of Rho GTPase activating proteins that contain a steroidogenic acute regulatory protein related lipid transfer domain. The encoded protein localizes to focal adhesions and may be involved in regulating cell morphology. This protein may also function as a tumor suppressor. [provided by RefSeq, Mar 2010]

STARD3 Gene

StAR-related lipid transfer (START) domain containing 3

This gene encodes a member of a subfamily of lipid trafficking proteins that are characterized by a C-terminal steroidogenic acute regulatory domain and an N-terminal metastatic lymph node 64 domain. The encoded protein localizes to the membranes of late endosomes and may be involved in exporting cholesterol. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]

STARD6 Gene

StAR-related lipid transfer (START) domain containing 6

Cholesterol homeostasis is regulated, at least in part, by sterol regulatory element (SRE)-binding proteins (e.g., SREBP1; MIM 184756) and by liver X receptors (e.g., LXRA; MIM 602423). Upon sterol depletion, LXRs are inactive and SREBPs are cleaved, after which they bind promoter SREs and activate genes involved in cholesterol biosynthesis and uptake. Sterol transport is mediated by vesicles or by soluble protein carriers, such as steroidogenic acute regulatory protein (STAR; MIM 600617). STAR is homologous to a family of proteins containing a 200- to 210-amino acid STAR-related lipid transfer (START) domain, including STARD6 (Soccio et al., 2002 [PubMed 12011452]).[supplied by OMIM, Mar 2008]

STARD7 Gene

StAR-related lipid transfer (START) domain containing 7

Predicted to enable lipid transfer activity. Predicted to be involved in ubiquinone biosynthetic process. Predicted to act upstream of or within several processes, including establishment of skin barrier; mucociliary clearance; and myeloid dendritic cell activation. Located in mitochondrion. Implicated in familial adult myoclonic epilepsy 2. [provided by Alliance of Genome Resources, Mar 2025]

TRN-GTT5-1 Gene

transfer RNA-Asn (GTT) 5-1

TRA-AGC20-1 Gene

transfer RNA-Ala (AGC) 20-1

TRY-GTA9-1 Gene

transfer RNA-Tyr (GTA) 9-1

TRC-GCA13-1 Gene

transfer RNA-Cys (GCA) 13-1

TRS-GCT6-1 Gene

transfer RNA-Ser (GCT) 6-1

TRE-CTC1-5 Gene

transfer RNA-Glu (CTC) 1-5

TRE-CTC1-3 Gene

transfer RNA-Glu (CTC) 1-3

TRN-GTT15-1 Gene

transfer RNA-Asn (GTT) 15-1

TRUND-NNN8-1 Gene

transfer RNA-undetermined (NNN) 8-1

TRD-GTC7-1 Gene

transfer RNA-Asp (GTC) 7-1

TRNAK-UUU Gene

transfer RNA lysine (anticodon UUU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRN-GTT23-1 Gene

transfer RNA-Asn (GTT) 23-1

TRS-GCT2-1 Gene

transfer RNA-Ser (GCT) 2-1

TRQ-TTG9-1 Gene

transfer RNA-Gln (TTG) 9-1

TRE-TTC9-1 Gene

transfer RNA-Glu (TTC) 9-1

TRNAI-AAU Gene

transfer RNA isoleucine (anticodon AAU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

GLTPP1 Gene

glycolipid transfer protein pseudogene 1

TRQ-TTG4-1 Gene

transfer RNA-Gln (TTG) 4-1

TRC-GCA25-1 Gene

transfer RNA-Cys (GCA) 25-1

TRP-CGG2-1 Gene

transfer RNA-Pro (CGG) 2-1

NMTRQ-CTG1-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (CTG) 1-1

TRS-GCT3-1 Gene

transfer RNA-Ser (GCT) 3-1

TRG-GCC3-1 Gene

transfer RNA-Gly (GCC) 3-1

TRR-CCT6-2 Gene

transfer RNA-Arg (CCT) 6-2

TRF-GAA1-6 Gene

transfer RNA-Phe (GAA) 1-6

TRF-GAA1-4 Gene

transfer RNA-Phe (GAA) 1-4

TRF-GAA1-5 Gene

transfer RNA-Phe (GAA) 1-5

TRF-GAA1-2 Gene

transfer RNA-Phe (GAA) 1-2

TRF-GAA1-3 Gene

transfer RNA-Phe (GAA) 1-3

TRF-GAA1-1 Gene

transfer RNA-Phe (GAA) 1-1

TRE-CTC2-1 Gene

transfer RNA-Glu (CTC) 2-1

TRNAN-GUU Gene

transfer RNA asparagine (anticodon GUU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRK-CTT1-2 Gene

transfer RNA-Lys (CTT) 1-2

TRK-CTT1-1 Gene

transfer RNA-Lys (CTT) 1-1

TRC-GCA24-1 Gene

transfer RNA-Cys (GCA) 24-1

TRG-GCC2-6 Gene

transfer RNA-Gly (GCC) 2-6

TRG-GCC2-4 Gene

transfer RNA-Gly (GCC) 2-4

TRG-GCC2-5 Gene

transfer RNA-Gly (GCC) 2-5

TRNAP-AGG Gene

transfer RNA proline (anticodon AGG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRQ-TTG10-1 Gene

transfer RNA-Gln (TTG) 10-1

TRE-CTC3-1 Gene

transfer RNA-Glu (CTC) 3-1

TRE-CTC6-1 Gene

transfer RNA-Glu (CTC) 6-1

TRNAV-AAC Gene

transfer RNA valine (anticodon AAC)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRSUP-CTA1-1 Gene

transfer RNA suppressor (CTA) 1-1

TRV-CAC11-1 Gene

transfer RNA-Val (CAC) 11-1

TRS-AGA4-1 Gene

transfer RNA-Ser (AGA) 4-1

TRE-TTC8-1 Gene

transfer RNA-Glu (TTC) 8-1

NMTRQ-TTG4-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 4-1

TRC-GCA3-1 Gene

transfer RNA-Cys (GCA) 3-1

TRNAS-GCU Gene

transfer RNA serine (anticodon GCU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

NMTRQ-TTG5-1 Gene

nuclear-encoded mitochondrial transfer RNA-Gln (TTG) 5-1

TRNAW-CCA Gene

transfer RNA tryptophan (anticodon CCA)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRX-CAT1-8 Gene

transfer RNA-iMet (CAT) 1-8

TRX-CAT1-3 Gene

transfer RNA-iMet (CAT) 1-3

TRX-CAT1-2 Gene

transfer RNA-iMet (CAT) 1-2

TRX-CAT1-1 Gene

transfer RNA-iMet (CAT) 1-1

TRX-CAT1-7 Gene

transfer RNA-iMet (CAT) 1-7

TRX-CAT1-6 Gene

transfer RNA-iMet (CAT) 1-6

TRX-CAT1-5 Gene

transfer RNA-iMet (CAT) 1-5

TRX-CAT1-4 Gene

transfer RNA-iMet (CAT) 1-4

TRNAL-AAG Gene

transfer RNA leucine (anticodon AAG)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

TRNAT-UGU Gene

transfer RNA threonine (anticodon UGU)

This record serves to anchor the annotations of this class of tRNAs at multiple locations on the human genome. The placements are predicted using tRNAscan-SE (Lowe, T.M. and Eddy, S.R. 1997. Nucleic Acids Res. 25:955-964, PubMed 9023104).

BLTP2 Gene

bridge-like lipid transfer protein family member 2

This gene was initially characterized in human as having high expression levels in breast carcinomas and breast cancer cell lines. This gene also has increased expression in prostrate cancer cells relative to normal prostrate tissues. Expression of this gene is negatively regulated by direct binding of the microRNA miR-195 to its 3' UTR. miR-195 has been shown to modulate the invasiveness of prostrate cancer cells and xenograft metastases by downgrading expression of this gene. In mouse, the protein encoded by this gene was identified as an antigen on acute monocytic leukemia cells. In human, alternative splicing results in multiple transcript variants encoding distinct isoforms; some of these isoforms are predicted to contain an RNA pol II promoter FMP27 protein domain and a Golgi-body-localization APT1 domain. [provided by RefSeq, Apr 2017]

BLTP1 Gene

bridge-like lipid transfer protein family member 1

This gene is located on the long arm of chromosome 4 in a region that is associated with susceptibility to celiac disease. The encoded protein is similar to a Chinese hamster protein that is associated with spermatocyte and adipocyte differentiation. The C-terminus of the protein is also similar to a Caenorhabditis elegans protein that plays a role in lipid storage. In mammals, this protein is thought to function in the regulation of epithelial growth and differentiation, and in tumor development. [provided by RefSeq, Oct 2009]

BLTP3B Gene

bridge-like lipid transfer protein family member 3B

Enables GARP complex binding activity; lipid transfer activity; and protein homodimerization activity. Involved in early endosome to Golgi transport and intermembrane lipid transfer. Located in cytosol and early endosome. [provided by Alliance of Genome Resources, Mar 2025]

BLTP3A Gene

bridge-like lipid transfer protein family member 3A

Enables histone deacetylase binding activity and identical protein binding activity. Located in late endosome. [provided by Alliance of Genome Resources, Mar 2025]

APOLTP Gene

apolipoprotein lipid transfer particle homolog

electron transfer flavoprotein-ubiquinone oxidoreductase defect Gene Set

From HPO Gene-Disease Associations

genes associated with the electron transfer flavoprotein-ubiquinone oxidoreductase defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Electron Transfer Flavoprotein-Ubiquinone Oxidoreductase Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

mitochondrial electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Electron transfer flavoprotein, alpha subunit, C-terminal, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein, alpha subunit, C-terminal, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein, beta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein, beta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein, alpha/beta-subunit, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein, alpha/beta-subunit, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein, alpha subunit, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein, alpha subunit, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein, beta-subunit, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein, beta-subunit, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein, alpha subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Electron transfer flavoprotein, alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Electron transfer flavoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Electron transfer flavoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Mitochondrial electron transfer flavoprotein complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Mitochondrial electron transfer flavoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

electron-transferring-flavoprotein dehydrogenase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the electron-transferring-flavoprotein dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

electron-transferring-flavoprotein dehydrogenase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the electron-transferring-flavoprotein dehydrogenase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

transmembrane electron transfer carrier Gene Set

From GO Molecular Function Annotations 2015

genes performing the transmembrane electron transfer carrier molecular function from the curated GO Molecular Function Annotations 2015 dataset.

negative regulation of electron transfer activity Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of electron transfer activity biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of electron transfer activity Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of electron transfer activity biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of electron transfer activity Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of electron transfer activity biological process from the curated GO Biological Process Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

flavoprotein Gene Set

From GeneRIF Biological Term Annotations

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

Flavoprotein pyridine nucleotide cytochrome reductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Flavoprotein pyridine nucleotide cytochrome reductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CO dehydrogenase flavoprotein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CO dehydrogenase flavoprotein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fumarate reductase/succinate dehydrogenase flavoprotein-like, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fumarate reductase/succinate dehydrogenase flavoprotein-like, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Succinate dehydrogenase, flavoprotein subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Succinate dehydrogenase, flavoprotein subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Succinate dehydrogenase/fumarate reductase flavoprotein, catalytic domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Succinate dehydrogenase/fumarate reductase flavoprotein, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Flavoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Flavoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Succinate dehydrogenase/fumarate reductase, flavoprotein subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Succinate dehydrogenase/fumarate reductase, flavoprotein subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

CO dehydrogenase flavoprotein-like, FAD-binding, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the CO dehydrogenase flavoprotein-like, FAD-binding, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DNA/pantothenate metabolism flavoprotein, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DNA/pantothenate metabolism flavoprotein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Flavoprotein-like Gene Set

From InterPro Predicted Protein Domain Annotations

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

electron Gene Set

From GeneRIF Biological Term Annotations

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

atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2015

genes participating in the atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2015 dataset.

mitochondrial electron transport, ubiquinol to cytochrome c Gene Set

From GO Biological Process Annotations 2015

genes participating in the mitochondrial electron transport, ubiquinol to cytochrome c biological process from the curated GO Biological Process Annotations 2015 dataset.

aerobic electron transport chain Gene Set

From GO Biological Process Annotations 2015

genes participating in the aerobic electron transport chain biological process from the curated GO Biological Process Annotations 2015 dataset.

mitochondrial atp synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2015

genes participating in the mitochondrial atp synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2015 dataset.

mitochondrial electron transport, cytochrome c to oxygen Gene Set

From GO Biological Process Annotations 2015

genes participating in the mitochondrial electron transport, cytochrome c to oxygen biological process from the curated GO Biological Process Annotations 2015 dataset.

electron transport chain Gene Set

From GO Biological Process Annotations 2015

genes participating in the electron transport chain biological process from the curated GO Biological Process Annotations 2015 dataset.

respiratory electron transport chain Gene Set

From GO Biological Process Annotations 2015

genes participating in the respiratory electron transport chain biological process from the curated GO Biological Process Annotations 2015 dataset.

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

From GO Molecular Function Annotations 2015

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 2015 dataset.

electron carrier activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the electron carrier activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

abnormal respiratory electron transport chain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal respiratory electron transport chain 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.

The citric acid (TCA) cycle and respiratory electron transport Gene Set

From Reactome Pathways 2014

proteins participating in the The citric acid (TCA) cycle and respiratory electron transport pathway from the Reactome Pathways dataset.

Electron transport from NADPH to Ferredoxin Gene Set

From Reactome Pathways 2014

proteins participating in the Electron transport from NADPH to Ferredoxin pathway from the Reactome Pathways dataset.

Respiratory electron transport Gene Set

From Reactome Pathways 2014

proteins participating in the Respiratory electron transport 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 2014

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

Electron Transport Chain(Homo sapiens) Gene Set

From WikiPathways Pathways 2014

proteins participating in the Electron Transport Chain(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

Electron Transport Chain(Mus musculus) Gene Set

From WikiPathways Pathways 2014

proteins participating in the Electron Transport Chain(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.

Electron Transport Chain Deficiencies, Mitochondrial Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Electron Transport Chain Deficiencies, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Glomerular Subendothelial Electron-Dense Deposits Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Glomerular Subendothelial Electron-Dense Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

mitochondrial electron transport, cytochrome c to oxygen Gene Set

From GO Biological Process Annotations 2023

genes participating in the mitochondrial electron transport, cytochrome c to oxygen biological process from the curated GO Biological Process Annotations 2023 dataset.

mitochondrial electron transport, ubiquinol to cytochrome c Gene Set

From GO Biological Process Annotations 2023

genes participating in the mitochondrial electron transport, ubiquinol to cytochrome c biological process from the curated GO Biological Process Annotations 2023 dataset.

mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2023 dataset.

respiratory electron transport chain Gene Set

From GO Biological Process Annotations 2023

genes participating in the respiratory electron transport chain biological process from the curated GO Biological Process Annotations 2023 dataset.

electron transport chain Gene Set

From GO Biological Process Annotations 2023

genes participating in the electron transport chain biological process from the curated GO Biological Process Annotations 2023 dataset.

plasma membrane ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the plasma membrane ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2023 dataset.

aerobic electron transport chain Gene Set

From GO Biological Process Annotations 2023

genes participating in the aerobic electron transport chain biological process from the curated GO Biological Process Annotations 2023 dataset.

electron transport coupled proton transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the electron transport coupled proton transport biological process from the curated GO Biological Process Annotations 2023 dataset.

ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2023 dataset.

abnormal respiratory electron transport chain Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal respiratory electron transport chain phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal mitochondrial ATP synthesis coupled electron transport Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal mitochondrial ATP synthesis coupled electron transport phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Electron transport chain OXPHOS system in mitochondria Gene Set

From WikiPathways Pathways 2024

proteins participating in the Electron transport chain OXPHOS system in mitochondria pathway from the WikiPathways Pathways 2024 dataset.

Aerobic respiration and respiratory electron transport Gene Set

From Reactome Pathways 2024

proteins participating in the Aerobic respiration and respiratory electron transport pathway from the Reactome Pathways 2024 dataset.

Electron transport from NADPH to Ferredoxin Gene Set

From Reactome Pathways 2024

proteins participating in the Electron transport from NADPH to Ferredoxin pathway from the Reactome Pathways 2024 dataset.

Respiratory electron transport Gene Set

From Reactome Pathways 2024

proteins participating in the Respiratory electron transport pathway from the Reactome Pathways 2024 dataset.

mitochondrial electron transport, cytochrome c to oxygen Gene Set

From GO Biological Process Annotations 2025

genes participating in the mitochondrial electron transport, cytochrome c to oxygen biological process from the curated GO Biological Process Annotations 2025 dataset.

mitochondrial electron transport, ubiquinol to cytochrome c Gene Set

From GO Biological Process Annotations 2025

genes participating in the mitochondrial electron transport, ubiquinol to cytochrome c biological process from the curated GO Biological Process Annotations 2025 dataset.

mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2025

genes participating in the mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2025 dataset.

respiratory electron transport chain Gene Set

From GO Biological Process Annotations 2025

genes participating in the respiratory electron transport chain biological process from the curated GO Biological Process Annotations 2025 dataset.

electron transport chain Gene Set

From GO Biological Process Annotations 2025

genes participating in the electron transport chain biological process from the curated GO Biological Process Annotations 2025 dataset.

aerobic electron transport chain Gene Set

From GO Biological Process Annotations 2025

genes participating in the aerobic electron transport chain biological process from the curated GO Biological Process Annotations 2025 dataset.

electron transport coupled proton transport Gene Set

From GO Biological Process Annotations 2025

genes participating in the electron transport coupled proton transport biological process from the curated GO Biological Process Annotations 2025 dataset.

ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2025

genes participating in the ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of mitochondrial ATP synthesis coupled electron transport Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of mitochondrial ATP synthesis coupled electron transport biological process from the curated GO Biological Process Annotations 2025 dataset.

Mitochondrial electron transport chain function Gene Set

From CM4AI U2OS Cell Map Protein Localization Assemblies

proteins comprising Mitochondrial electron transport chain function assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.

cholesteryl ester transfer protein Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesteryl ester transfer protein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cholesteryl ester transfer protein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesteryl ester transfer protein plasma lipid levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesteryl ester transfer protein plasma lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

transfer Gene Set

From GeneRIF Biological Term Annotations

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

phospholipid transfer to membrane Gene Set

From GO Biological Process Annotations 2015

genes participating in the phospholipid transfer to membrane biological process from the curated GO Biological Process Annotations 2015 dataset.

transferase activity, transferring acyl groups, acyl groups converted into alkyl on transfer Gene Set

From GO Molecular Function Annotations 2015

genes performing the transferase activity, transferring acyl groups, acyl groups converted into alkyl on transfer molecular function from the curated GO Molecular Function Annotations 2015 dataset.

Transfer Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Transfer phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Glycolipid transfer protein domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glycolipid transfer protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

StAR-related lipid transfer protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the StAR-related lipid transfer protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cholesteryl ester transfer Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cholesteryl ester transfer protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phospholipid transfer protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phospholipid transfer protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

StAR-related lipid transfer protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the StAR-related lipid transfer protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Phosphatidylinositol transfer protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Phosphatidylinositol transfer protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transfer of LPS from LBP carrier to CD14 Gene Set

From Reactome Pathways 2014

proteins participating in the Transfer of LPS from LBP carrier to CD14 pathway from the Reactome Pathways dataset.

Prefoldin mediated transfer of substrate to CCT/TriC Gene Set

From Reactome Pathways 2014

proteins participating in the Prefoldin mediated transfer of substrate to CCT/TriC pathway from the Reactome Pathways dataset.

Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Set

From Reactome Pathways 2014

proteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways dataset.

Cholesteryl Ester Transfer Protein Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cholesteryl Ester Transfer Protein Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Fetus Affected By Placental Transfer Of Anticonvulsant Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Fetus Affected By Placental Transfer Of Anticonvulsant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cholesteryl Ester Transfer Protein Measurement Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cholesteryl Ester Transfer Protein Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

intermembrane lipid transfer Gene Set

From GO Biological Process Annotations 2023

genes participating in the intermembrane lipid transfer biological process from the curated GO Biological Process Annotations 2023 dataset.

protein maturation by copper ion transfer Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein maturation by copper ion transfer biological process from the curated GO Biological Process Annotations 2023 dataset.

protein insertion into ER membrane by stop-transfer membrane-anchor sequence Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein insertion into ER membrane by stop-transfer membrane-anchor sequence biological process from the curated GO Biological Process Annotations 2023 dataset.

protein maturation by iron-sulfur cluster transfer Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein maturation by iron-sulfur cluster transfer biological process from the curated GO Biological Process Annotations 2023 dataset.

protein maturation by [2Fe-2S] cluster transfer Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein maturation by [2Fe-2S] cluster transfer biological process from the curated GO Biological Process Annotations 2023 dataset.

protein maturation by [4Fe-4S] cluster transfer Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein maturation by [4Fe-4S] cluster transfer biological process from the curated GO Biological Process Annotations 2023 dataset.

intermembrane sphingolipid transfer Gene Set

From GO Biological Process Annotations 2023

genes participating in the intermembrane sphingolipid transfer biological process from the curated GO Biological Process Annotations 2023 dataset.

phosphatidylinositol transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phosphatidylinositol transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

phosphatidic acid transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phosphatidic acid transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

cholesterol transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the cholesterol transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

sterol transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the sterol transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

phosphatidylcholine transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phosphatidylcholine transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

sphingomyelin transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the sphingomyelin transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

phospholipid transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phospholipid transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

diacylglyceride transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the diacylglyceride transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

phosphatidylglycerol transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phosphatidylglycerol transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

cerebroside transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the cerebroside transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

phosphatidylethanolamine transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phosphatidylethanolamine transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

triglyceride transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the triglyceride transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

ceramide 1-phosphate transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the ceramide 1-phosphate transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

glycolipid transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the glycolipid transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

phosphatidylserine transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the phosphatidylserine transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

ceramide transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the ceramide transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

sphingolipid transfer activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the sphingolipid transfer activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

acyltransferase activity, acyl groups converted into alkyl on transfer Gene Set

From GO Molecular Function Annotations 2023

genes performing the acyltransferase activity, acyl groups converted into alkyl on transfer molecular function from the curated GO Molecular Function Annotations 2023 dataset.

Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Set

From Reactome Pathways 2024

proteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways 2024 dataset.

Prefoldin mediated transfer of substrate to CCT/TriC Gene Set

From Reactome Pathways 2024

proteins participating in the Prefoldin mediated transfer of substrate to CCT/TriC pathway from the Reactome Pathways 2024 dataset.

Transfer of LPS from LBP carrier to CD14 Gene Set

From Reactome Pathways 2024

proteins participating in the Transfer of LPS from LBP carrier to CD14 pathway from the Reactome Pathways 2024 dataset.

intermembrane lipid transfer Gene Set

From GO Biological Process Annotations 2025

genes participating in the intermembrane lipid transfer biological process from the curated GO Biological Process Annotations 2025 dataset.

protein insertion into ER membrane by stop-transfer membrane-anchor sequence Gene Set

From GO Biological Process Annotations 2025

genes participating in the protein insertion into ER membrane by stop-transfer membrane-anchor sequence biological process from the curated GO Biological Process Annotations 2025 dataset.

intermembrane sphingolipid transfer Gene Set

From GO Biological Process Annotations 2025

genes participating in the intermembrane sphingolipid transfer biological process from the curated GO Biological Process Annotations 2025 dataset.

phosphatidylinositol transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phosphatidylinositol transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

cholesterol transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the cholesterol transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

phosphatidic acid transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phosphatidic acid transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

sterol transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the sterol transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

phosphatidylcholine transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phosphatidylcholine transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

sphingomyelin transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the sphingomyelin transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

phospholipid transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phospholipid transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

diacylglyceride transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the diacylglyceride transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

phosphatidylglycerol transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phosphatidylglycerol transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

cerebroside transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the cerebroside transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

phosphatidylethanolamine transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phosphatidylethanolamine transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

triglyceride transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the triglyceride transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

ceramide 1-phosphate transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the ceramide 1-phosphate transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

glycolipid transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the glycolipid transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

phosphatidylserine transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the phosphatidylserine transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

ceramide transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the ceramide transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

sphingolipid transfer activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the sphingolipid transfer activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

acyltransferase activity, acyl groups converted into alkyl on transfer Gene Set

From GO Molecular Function Annotations 2025

genes performing the acyltransferase activity, acyl groups converted into alkyl on transfer molecular function from the curated GO Molecular Function Annotations 2025 dataset.

cholesterol-ester transfer protein deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease cholesterol-ester transfer protein deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Transfer cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Transfer cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Transfer cell precursor Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Transfer cell precursor in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

iron-sulfur cluster transfer complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the iron-sulfur cluster transfer complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Cholesteryl ester transfer protein levels Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Cholesteryl ester transfer protein levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

oxidoreductase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

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

oxidoreductase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

cytochrome p450 oxidoreductase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cytochrome p450 oxidoreductase in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oxidoreductase Gene Set

From GeneRIF Biological Term Annotations

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

sulfide oxidation, using sulfide:quinone oxidoreductase Gene Set

From GO Biological Process Annotations 2015

genes participating in the sulfide oxidation, using sulfide:quinone oxidoreductase biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2015 dataset.

oxidoreductase complex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the oxidoreductase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

n1-acetylspermidine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the n1-acetylspermidine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on superoxide radicals as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on superoxide radicals as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

aminoacetone:oxygen oxidoreductase(deaminating) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the aminoacetone:oxygen oxidoreductase(deaminating) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

intramolecular oxidoreductase activity, interconverting aldoses and ketoses Gene Set

From GO Molecular Function Annotations 2015

genes performing the intramolecular oxidoreductase activity, interconverting aldoses and ketoses molecular function from the curated GO Molecular Function Annotations 2015 dataset.

n1-acetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the n1-acetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

peptide disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the peptide disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on iron-sulfur proteins as donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on ch or ch2 groups, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on ch or ch2 groups, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on diphenols and related substances as donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

glutathione disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the glutathione disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on peroxide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on peroxide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

n1-acetylspermine:oxygen oxidoreductase (n1-acetylspermidine-forming) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the n1-acetylspermine:oxygen oxidoreductase (n1-acetylspermidine-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of two atoms of oxygen into one donor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on nad(p)h Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on nad(p)h molecular function from the curated GO Molecular Function Annotations 2015 dataset.

intramolecular oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the intramolecular oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, oxidizing metal ions with flavin as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, oxidizing metal ions with flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

alditol:nadp+ 1-oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the alditol:nadp+ 1-oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-ch group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-ch group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

n(1),n(12)-diacetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the n(1),n(12)-diacetylspermine:oxygen oxidoreductase (3-acetamidopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on ch or ch2 groups Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on ch or ch2 groups molecular function from the curated GO Molecular Function Annotations 2015 dataset.

sulfide:quinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the sulfide:quinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

spermine:oxygen oxidoreductase (spermidine-forming) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the spermine:oxygen oxidoreductase (spermidine-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

intramolecular oxidoreductase activity, transposing c=c bonds Gene Set

From GO Molecular Function Annotations 2015

genes performing the intramolecular oxidoreductase activity, transposing c=c bonds molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, oxidizing metal ions, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, oxidizing metal ions, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

tryptamine:oxygen oxidoreductase (deaminating) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the tryptamine:oxygen oxidoreductase (deaminating) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

protein disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the protein disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a sulfur group of donors, nad(p) as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

glutathione oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the glutathione oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

norspermine:oxygen oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the norspermine:oxygen oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a heme group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a heme group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, with nad(p)h as one donor, and the other dehydrogenated molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on nad(p)h, nad(p) as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on nad(p)h, nad(p) as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, oxidizing metal ions, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, oxidizing metal ions, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

intramolecular oxidoreductase activity, transposing s-s bonds Gene Set

From GO Molecular Function Annotations 2015

genes performing the intramolecular oxidoreductase activity, transposing s-s bonds molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on nad(p)h, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on nad(p)h, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, oxidizing metal ions Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, oxidizing metal ions molecular function from the curated GO Molecular Function Annotations 2015 dataset.

nadph:sulfur oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the nadph:sulfur oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a heme group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

spermidine:oxygen oxidoreductase (3-aminopropanal-forming) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the spermidine:oxygen oxidoreductase (3-aminopropanal-forming) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on ch or ch2 groups, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on ch or ch2 groups, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on ch-oh group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on ch-oh group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on diphenols and related substances as donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, nad(p)h as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

intramolecular oxidoreductase activity, interconverting keto- and enol-groups Gene Set

From GO Molecular Function Annotations 2015

genes performing the intramolecular oxidoreductase activity, interconverting keto- and enol-groups molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a sulfur group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a sulfur group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2015 dataset.

phenethylamine:oxygen oxidoreductase (deaminating) activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the phenethylamine:oxygen oxidoreductase (deaminating) activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on phosphorus or arsenic in donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on phosphorus or arsenic in donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on ch or ch2 groups, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on ch or ch2 groups, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on nad(p)h, nitrogenous group as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on nad(p)h, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on nad(p)h, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-nh group of donors Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-nh group of donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on ch or ch2 groups, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on ch or ch2 groups, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-oh group of donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

glyceraldehyde oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the glyceraldehyde oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on nad(p)h, heme protein as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on nad(p)h, heme protein as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on the ch-ch group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

NADH:quinone oxidoreductase/Mrp antiporter, membrane subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH:quinone oxidoreductase/Mrp antiporter, membrane subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, molybdopterin-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, molybdopterin-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdopterin oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdopterin oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Moybdenum cofactor oxidoreductase, dimerisation Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Moybdenum cofactor oxidoreductase, dimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NAD(P)H-quinone oxidoreductase subunit D/H Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NAD(P)H-quinone oxidoreductase subunit D/H protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, FAD/NAD(P)-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, FAD/NAD(P)-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, NAD-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, NAD-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, FAD-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, FAD-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase subunit E-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase subunit E-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase-like, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase-like, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, class I, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, class I, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Quinone oxidoreductase/zeta-crystallin, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Quinone oxidoreductase/zeta-crystallin, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, chain G, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, chain G, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, chain M/4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, chain M/4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Pyridine nucleotide-disulphide oxidoreductase, class-II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pyridine nucleotide-disulphide oxidoreductase, class-II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, subunit D Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, subunit D protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

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

FAD dependent oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD dependent oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-plastoquinone oxidoreductase, chain 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-plastoquinone oxidoreductase, chain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Malic oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Malic oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Eukaryotic molybdopterin oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Eukaryotic molybdopterin oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-dependent pyridine nucleotide-disulphide oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-dependent pyridine nucleotide-disulphide oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADH-quinone oxidoreductase, chain I Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADH-quinone oxidoreductase, chain I protein domain from the InterPro Predicted Protein Domain Annotations dataset.

FAD-linked oxidoreductase-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FAD-linked oxidoreductase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase FAD/NAD(P)-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase FAD/NAD(P)-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADP-dependent oxidoreductase domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADP-dependent oxidoreductase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Multi-copper polyphenol oxidoreductase, laccase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Multi-copper polyphenol oxidoreductase, laccase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Oxidoreductase, molybdopterin binding site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Oxidoreductase, molybdopterin binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Quinone oxidoreductase PIG3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Quinone oxidoreductase PIG3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

NADPH-dependent diflavin oxidoreductase 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the NADPH-dependent diflavin oxidoreductase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transketolase, C-terminal/Pyruvate-ferredoxin oxidoreductase, domain II Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transketolase, C-terminal/Pyruvate-ferredoxin oxidoreductase, domain II protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Molybdopterin oxidoreductase, 4Fe-4S domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Molybdopterin oxidoreductase, 4Fe-4S domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

disordered steroidogenesis due to cytochrome p450 oxidoreductase Gene Set

From OMIM Gene-Disease Associations

genes associated with the disordered steroidogenesis due to cytochrome p450 oxidoreductase phenotype from the curated OMIM Gene-Disease Associations dataset.

positive regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2023 dataset.

sulfide oxidation, using sulfide:quinone oxidoreductase Gene Set

From GO Biological Process Annotations 2023

genes participating in the sulfide oxidation, using sulfide:quinone oxidoreductase biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

alditol:NADP+ 1-oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the alditol:NADP+ 1-oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

glyceraldehyde oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the glyceraldehyde oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

glutathione disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the glutathione disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

intramolecular oxidoreductase activity, transposing C=C bonds Gene Set

From GO Molecular Function Annotations 2023

genes performing the intramolecular oxidoreductase activity, transposing C=C bonds molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on metal ions, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on metal ions, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

spermine:oxygen oxidoreductase (spermidine-forming) activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the spermine:oxygen oxidoreductase (spermidine-forming) activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

sulfide:quinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the sulfide:quinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

glutathione-dependent sulfide quinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the glutathione-dependent sulfide quinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on metal ions, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on metal ions, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on CH or CH2 groups, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on CH or CH2 groups, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

intramolecular oxidoreductase activity, interconverting aldoses and ketoses Gene Set

From GO Molecular Function Annotations 2023

genes performing the intramolecular oxidoreductase activity, interconverting aldoses and ketoses molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

intramolecular oxidoreductase activity, interconverting keto- and enol-groups Gene Set

From GO Molecular Function Annotations 2023

genes performing the intramolecular oxidoreductase activity, interconverting keto- and enol-groups molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on CH or CH2 groups, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on CH or CH2 groups, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

L-methionine:thioredoxin-disulfide S-oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the L-methionine:thioredoxin-disulfide S-oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

oxidoreductase activity, acting on NAD(P)H, NAD(P) as acceptor Gene Set

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on NAD(P)H, NAD(P) as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

positive regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2025 dataset.

sulfide oxidation, using sulfide:quinone oxidoreductase Gene Set

From GO Biological Process Annotations 2025

genes participating in the sulfide oxidation, using sulfide:quinone oxidoreductase biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of oxidoreductase activity Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of oxidoreductase activity biological process from the curated GO Biological Process Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on metal ions, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on metal ions, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

glyceraldehyde oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the glyceraldehyde oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

glutathione disulfide oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the glutathione disulfide oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

intramolecular oxidoreductase activity, transposing C=C bonds Gene Set

From GO Molecular Function Annotations 2025

genes performing the intramolecular oxidoreductase activity, transposing C=C bonds molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on diphenols and related substances as donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on metal ions, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on metal ions, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

sulfide:quinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the sulfide:quinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

glutathione-dependent sulfide quinone oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the glutathione-dependent sulfide quinone oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with oxidation of a pair of donors resulting in the reduction of molecular oxygen to two molecules of water molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced pteridine as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on CH or CH2 groups, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on CH or CH2 groups, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

intramolecular oxidoreductase activity, interconverting aldoses and ketoses Gene Set

From GO Molecular Function Annotations 2025

genes performing the intramolecular oxidoreductase activity, interconverting aldoses and ketoses molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced ascorbate as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, with a flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

intramolecular oxidoreductase activity, interconverting keto- and enol-groups Gene Set

From GO Molecular Function Annotations 2025

genes performing the intramolecular oxidoreductase activity, interconverting keto- and enol-groups molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, another compound as one donor, and incorporation of one atom of oxygen molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH2 group of donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-CH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the aldehyde or oxo group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on CH or CH2 groups, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on CH or CH2 groups, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on CH or CH2 groups, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on NAD(P)H as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on NAD(P)H as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, oxygen as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on phosphorus or arsenic in donors, disulfide as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-NH group of donors, flavin as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on a sulfur group of donors, quinone or similar compound as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor Gene Set

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on the CH-OH group of donors, cytochrome as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

L-methionine:thioredoxin-disulfide S-oxidoreductase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the L-methionine:thioredoxin-disulfide S-oxidoreductase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Cytochrome P450 oxidoreductase deficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Cytochrome P450 oxidoreductase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Cytochrome P450 oxidoreductase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cytochrome P450 oxidoreductase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Oxidoreductase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Oxidoreductase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Oxidoreductase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Oxidoreductase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Dandy-Walker like malformation with atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dandy-Walker like malformation with atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Protan defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac conduction defect, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac conduction defect, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 7 with or without atrioventricular conduction defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 7 with or without atrioventricular conduction defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-Barr virus infection, and neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neutral 1 amino acid transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ventricular septal defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ventricular septal defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Laron-type isolated somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Laron-type isolated somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iodotyrosine deiodination defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to thrombomodulin defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal carnitine transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrioventricular septal defect 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrioventricular septal defect 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency due to defect in cd3-zeta Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency due to defect in cd3-zeta phenotype from the curated ClinVar Gene-Phenotype Associations 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.

Atrial septal defect 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Atrial septal defect 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Atrial septal defect 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oocyte maturation defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immune dysfunction with T-cell inactivation due to calcium entry defect 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iodotyrosyl coupling defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, X-Linked, Due To Factor Ix Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thrombophilia, X-Linked, Due To Factor Ix Defect from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

Cardiac Conduction Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Conduction Defect from the curated CTD Gene-Disease Associations dataset.

Atrial septal defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial septal defect 2 from the curated CTD Gene-Disease Associations dataset.

ATRIOVENTRICULAR SEPTAL DEFECT 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIOVENTRICULAR SEPTAL DEFECT 3 from the curated CTD Gene-Disease Associations dataset.

Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrioventricular Septal Defect, Partial, with Heterotaxy Syndrome from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.

METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease METHYLMALONIC ACIDURIA DUE TO TRANSCOBALAMIN RECEPTOR DEFECT from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 4 from the curated CTD Gene-Disease Associations dataset.

Atrioventricular Canal Defect Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrioventricular Canal Defect from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.

Neural tube defect, folate-sensitive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neural tube defect, folate-sensitive from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 6 from the curated CTD Gene-Disease Associations dataset.

NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency due to Defect in CD3-Zeta Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in CD3-Zeta from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 5 from the curated CTD Gene-Disease Associations dataset.

Atrial Septal Defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrial Septal Defect 1 from the curated CTD Gene-Disease 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.

Immunodeficiency due to Defect in MAPBP-Interacting Protein Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency due to Defect in MAPBP-Interacting Protein from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1 from the curated CTD Gene-Disease Associations dataset.

Immune dysfunction with T-cell inactivation due to calcium entry defect 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immune dysfunction with T-cell inactivation due to calcium entry defect 2 from the curated CTD Gene-Disease Associations dataset.

ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATRIAL SEPTAL DEFECT 7 WITH OR WITHOUT ATRIOVENTRICULAR CONDUCTION DEFECTS from the curated CTD Gene-Disease Associations dataset.

atrial heart septal defect Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease atrial heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart septal defect Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease heart septal defect from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

alcohol-related birth defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease alcohol-related birth defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrioventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital bile acid synthesis defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atrial heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

qualitative platelet defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

human spermatogenic defect Gene Set

From GAD Gene-Disease Associations

genes associated with the disease human spermatogenic defect in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

defect Gene Set

From GeneRIF Biological Term Annotations

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

conotruncal defect Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the conotruncal defect phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

thyroid hormone receptor defect Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid hormone receptor defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline defect of mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the midline defect of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

secundum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the secundum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dynein arm defect of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the dynein arm defect of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inlet ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the inlet ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thyroid defect in oxidation and organification of iodide Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid defect in oxidation and organification of iodide phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenocorticotropin (acth) receptor (acthr) defect Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenocorticotropin (acth) receptor (acthr) defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sacral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the sacral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abdominal wall defect Gene Set

From HPO Gene-Disease Associations

genes associated with the abdominal wall defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

visual field defect Gene Set

From HPO Gene-Disease Associations

genes associated with the visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrioventricular canal defect with right ventricle aorta and pulmonary atresia Gene Set

From HPO Gene-Disease Associations

genes associated with the atrioventricular canal defect with right ventricle aorta and pulmonary atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscular ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the muscular ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

defect in the atrial septum Gene Set

From HPO Gene-Disease Associations

genes associated with the defect in the atrial septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

skull defect Gene Set

From HPO Gene-Disease Associations

genes associated with the skull defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cervical segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

perimembranous ventricular septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the perimembranous ventricular septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline defect of the nose Gene Set

From HPO Gene-Disease Associations

genes associated with the midline defect of the nose phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

complete atrioventricular canal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the complete atrioventricular canal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

large central visual field defect Gene Set

From HPO Gene-Disease Associations

genes associated with the large central visual field defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

conotruncal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the conotruncal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

primum atrial septal defect Gene Set

From HPO Gene-Disease Associations

genes associated with the primum atrial septal defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Mannose-P-dolichol utilization defect 1 protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Mannose-P-dolichol utilization defect 1 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

perimembraneous ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

partial atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

inlet ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle with atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

iodide oxidation defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aorticopulmonary septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

double outlet right ventricle, ventricular defect committed to aorta Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

muscular ventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium primum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

complete atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ostium secundum atrial septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrioventricular septal defect Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thrombophilia due to thrombomodulin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombomodulin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

bleeding disorder due to p2rx1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the bleeding disorder due to p2rx1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

schizophrenia, neurophysiologic defect in Gene Set

From OMIM Gene-Disease Associations

genes associated with the schizophrenia, neurophysiologic defect in phenotype from the curated OMIM Gene-Disease Associations dataset.

{atrioventricular septal defect, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

?isolated growth hormone deficiency due to defect in ghrf Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?isolated growth hormone deficiency due to defect in ghrf phenotype from the curated OMIM Gene-Disease Associations dataset.

erythrocyte lactate transporter defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the erythrocyte lactate transporter defect phenotype from the curated OMIM Gene-Disease Associations dataset.

natural killer cell and glucocorticoid deficiency with dna repair defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the natural killer cell and glucocorticoid deficiency with dna repair defect phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

selective t-cell defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the selective t-cell defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypercholesterolemia, familial, due to ldlr defect, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypercholesterolemia, familial, due to ldlr defect, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect, partial, with heterotaxy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect, partial, with heterotaxy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

bile acid synthesis defect, congenital, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the bile acid synthesis defect, congenital, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

ventricular septal defect 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ventricular septal defect 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac conduction defect, nonspecific Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac conduction defect, nonspecific phenotype from the curated OMIM Gene-Disease Associations dataset.

rickets due to defect in vitamin d 25-hydroxylation Gene Set

From OMIM Gene-Disease Associations

genes associated with the rickets due to defect in vitamin d 25-hydroxylation phenotype from the curated OMIM Gene-Disease Associations dataset.

{atrioventricular septal defect, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {atrioventricular septal defect, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

oocyte maturation defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the oocyte maturation defect phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria due to transcobalamin receptor defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria due to transcobalamin receptor defect phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

atrioventricular septal defect 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrioventricular septal defect 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia, x-linked, due to factor ix defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia, x-linked, due to factor ix defect phenotype from the curated OMIM Gene-Disease Associations dataset.

atrial septal defect 7, with or without av conduction defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the atrial septal defect 7, with or without av conduction defects phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency due to defect in mapbp-interacting protein Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency due to defect in mapbp-interacting protein phenotype from the curated OMIM Gene-Disease Associations dataset.

goiter, familial, due to ttf-1 defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the goiter, familial, due to ttf-1 defect phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency, x-linked, with magnesium defect, epstein-barr virus infection and neoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to thrombin defect Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to thrombin defect phenotype from the curated OMIM Gene-Disease Associations dataset.

{cardiac conduction defect, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {cardiac conduction defect, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type Gene Set

From OMIM Gene-Disease Associations

genes associated with the methylmalonic aciduria, vitamin b12-responsive, due to defect in synthesis of adenosylcobalamin, cblb complementation type phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) Gene Set

From Reactome Pathways 2014

proteins participating in the Defective CYP7B1 causes Spastic paraplegia 5A, autosomal recessive (SPG5A) and Congenital bile acid synthesis defect 3 (CBAS3) pathway from the Reactome Pathways dataset.

Histidinuria Renal Tubular Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Histidinuria Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bile Acid Synthesis Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bile Acid Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Renal Carnitine Transport Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Renal Carnitine Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atrioventricular Canal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atrioventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atrioventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Aortopulmonary Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Aortopulmonary Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atrial Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ostium Secundum Atrial Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ostium Secundum Atrial Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Alcohol Related Birth Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Alcohol Related Birth Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Glucose-6-Phosphate Transport Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Glucose-6-Phosphate Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventilatory Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Calvarial Skull Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Calvarial Skull Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Single Ventricle Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Single Ventricle Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Defect Of Skull And Scalp Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Defect Of Skull And Scalp in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Coronary Sinus Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Coronary Sinus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Muscular Ventricular Septum Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Muscular Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Perimembranous Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Perimembranous Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Triple Gene Defect Alpha Thalassemia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Triple Gene Defect Alpha Thalassemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Defect Of Vertebral Segmentation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Defect Of Vertebral Segmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Glycosylphosphatidylinositol Biosynthesis Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Glycosylphosphatidylinositol Biosynthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cardiac Conduction Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Patent Or Persistent Ostium Secundum Defect (Type Ii) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Patent Or Persistent Ostium Secundum Defect (Type Ii) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Patent Or Persistent Sinus Venosus Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Patent Or Persistent Sinus Venosus Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Antibody Deficiency Due To Defect In Cd19 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Antibody Deficiency Due To Defect In Cd19 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Conotruncal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Conotruncal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Obstructive Ventilatory Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Obstructive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Atrioventricular Septal Defect, Partial, With Heterotaxy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Partial Defect Of Atrioventricular Canal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Partial Defect Of Atrioventricular Canal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Synthetic Defect Of Bile Acids Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Synthetic Defect Of Bile Acids in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Bile Acid Synthesis Defect Type 3 Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Bile Acid Synthesis Defect Type 3 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Transitional Atrioventricular Canal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Transitional Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hereditary Bundle Branch System Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hereditary Bundle Branch System Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Midline Defect Of The Nose Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Midline Defect Of The Nose in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Thyroid Hormone Plasma Membrane Transport Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thyroid Hormone Plasma Membrane Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Defect Of Articular Cartilage Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Defect Of Articular Cartilage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Thoracoabdominal Wall Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thoracoabdominal Wall Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pulmonary Atresia With Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pulmonary Atresia With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Membranous Ventricular Septum Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Membranous Ventricular Septum Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Defect Of The Pericardium Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Defect Of The Pericardium in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Insulin Receptor, Defect In Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Insulin Receptor, Defect In in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Iodide Transport Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Iodide Transport Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neural Tube Defect, Folate-Sensitive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neural Tube Defect, Folate-Sensitive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Double Outlet Right Ventricle With Doubly Committed Ventricular Septal Defect And Pulmonary Stenosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Adenosylcobalamin Synthesis Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Adenosylcobalamin Synthesis Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Oocyte Maturation Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Oocyte Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Sacral Defect And Anterior Sacral Meningocele Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Sacral Defect And Anterior Sacral Meningocele in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Renal Tubular Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Renal Tubular Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenitally Corrected Transposition Of The Great Arteries With Ventricular Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cardiac Valvular Defect, Developmental Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cardiac Valvular Defect, Developmental in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ulnar-Fibular Ray Defect And Brachydactyly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ulnar-Fibular Ray Defect And Brachydactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cardiac Conduction Defect, Nonprogressive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cardiac Conduction Defect, Nonprogressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Corneal Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Corneal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Fibrinolytic Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Fibrinolytic Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Erythrocyte Lactate Transporter Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Erythrocyte Lactate Transporter Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Mondini Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Mondini Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Heart Defect, Tongue Hamartoma And Polysyndactyly Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Heart Defect, Tongue Hamartoma And Polysyndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Mucociliary Clearance Defect Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Mucociliary Clearance Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Adrenocorticotropin Receptor Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Adrenocorticotropin Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Color Vision Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Color Vision Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Maturation Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Maturation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Restrictive Ventilatory Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Restrictive Ventilatory Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Heart Defect (In Some Patients) Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Heart Defect (In Some Patients) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cardiac Conduction Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cardiac Conduction Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Retinal Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Retinal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Glaucomatous Visual Field Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Glaucomatous Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Dynein Arm Defect Of Respiratory Motile Cilia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Dynein Arm Defect Of Respiratory Motile Cilia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Iris Transillumination Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Iris Transillumination Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Iodide Organification Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Iodide Organification Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cervical Segmentation Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cervical Segmentation Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Lacrimal Duct Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Lacrimal Duct Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Large Central Visual Field Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Large Central Visual Field Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Unbalanced Atrioventricular Canal Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Unbalanced Atrioventricular Canal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Afferent Pupillary Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Afferent Pupillary Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventral Septal Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventral Septal Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Thyroid Defect In Oxidation And Organification Of Iodide Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Thyroid Defect In Oxidation And Organification Of Iodide in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Activating Thyroid-Stimulating Hormone Receptor Defect Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Activating Thyroid-Stimulating Hormone Receptor Defect in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

perimembraneous ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the perimembraneous ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

double outlet right ventricle with atrioventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the double outlet right ventricle with atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrial septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrioventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ostium secundum atrial septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ostium secundum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

complete atrioventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the complete atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

muscular ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the muscular ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ostium primum atrial septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ostium primum atrial septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

inlet ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the inlet ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

aorticopulmonary septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the aorticopulmonary septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

iodide oxidation defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the iodide oxidation defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

partial atrioventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the partial atrioventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

double outlet right ventricle, ventricular defect committed to aorta Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the double outlet right ventricle, ventricular defect committed to aorta phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

double outlet right ventricle, noncommitted ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the double outlet right ventricle, noncommitted ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

subarterial ventricular septal defect Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the subarterial ventricular septal defect phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

repair of mitotic kinetochore microtubule attachment defect Gene Set

From GO Biological Process Annotations 2025

genes participating in the repair of mitotic kinetochore microtubule attachment defect biological process from the curated GO Biological Process Annotations 2025 dataset.

Atrial heart septal defect Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Atrial heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Heart septal defect Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Heart septal defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Neural tube defect Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Neural tube defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Congenital bile acid synthesis defect from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect 2 Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Congenital bile acid synthesis defect 2 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Neural tube defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neural tube defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Ventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Ventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrioventricular septal defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrioventricular septal defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital bile acid synthesis defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect 5 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital bile acid synthesis defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 9 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Glycosylphosphatidylinositol biosynthesis defect 16 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Glycosylphosphatidylinositol biosynthesis defect 16 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 6 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 5 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Thrombophilia due to thrombin defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Thrombophilia due to thrombin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Qualitative platelet defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Qualitative platelet defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital bile acid synthesis defect 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital bile acid synthesis defect 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Joubert syndrome with orofaciodigital defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Joubert syndrome with orofaciodigital defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

X-linked thrombophilia due to factor IX defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease X-linked thrombophilia due to factor IX defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Atrial heart septal defect 8 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Atrial heart septal defect 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Developmental cardiac valvular defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Developmental cardiac valvular defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Congenital bile acid synthesis defect 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Congenital bile acid synthesis defect 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease hypotrichosis-lymphedema-telangiectasia-renal defect syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Thrombophilia due to thrombomodulin defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Thrombophilia due to thrombomodulin defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Nerve fibre bundle defect Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Nerve fibre bundle defect in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Combined oxidative phosphorylation defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Thyroglobulin synthesis defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Thyroglobulin synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Iodotyrosine deiodination defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Iodotyrosine deiodination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neutral 1 amino acid transport defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neutral 1 amino acid transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Congenital bile acid synthesis defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Congenital bile acid synthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Thrombophilia due to thrombin defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Thrombophilia due to thrombin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Iris transillumination defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Iris transillumination defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hepatoencephalopathy due to combined oxidative phosphorylation defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hepatoencephalopathy due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atrial septal defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atrial septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Fatal mitochondrial disease due to combined oxidative phosphorylation defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Fatal mitochondrial disease due to combined oxidative phosphorylation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Renal carnitine transport defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Renal carnitine transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Peroxisome biogenesis disorder due to PEX1 defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Peroxisome biogenesis disorder due to PEX1 defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Laron- somatotropin defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Laron- somatotropin defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Color vision defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Color vision defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Protan defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Protan defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Iodotyrosyl coupling defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Iodotyrosyl coupling defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MPV17-related mitochondrial DNA maintenance defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MPV17-related mitochondrial DNA maintenance defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Neural tube defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Neural tube defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Gastrointestinal defect and immunodeficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Gastrointestinal defect and immunodeficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Familial atrioventricular septal defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial atrioventricular septal defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Single Ventricle Defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Single Ventricle Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Heart defect - tongue hamartoma - polysyndactyly syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Heart defect - tongue hamartoma - polysyndactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Metabolic myopathy due to lactate transporter defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Metabolic myopathy due to lactate transporter defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Methylmalonic acidemia due to transcobalamin receptor defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Methylmalonic acidemia due to transcobalamin receptor defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Sacral defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Sacral defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Bile acid conjugation defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Bile acid conjugation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Ulnar/fibula ray defect-brachydactyly syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Ulnar/fibula ray defect-brachydactyly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Immunodeficiency due to defect in CD3-gamma Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Immunodeficiency due to defect in CD3-gamma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Thyroid Hormonogenesis Defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Thyroid Hormonogenesis Defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Oocyte maturation defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Glycosylphosphatidylinositol biosynthesis defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Glycosylphosphatidylinositol biosynthesis defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Inherited oocyte maturation defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Inherited oocyte maturation defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atrioventricular septal defect and common atrioventricular junction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atrioventricular septal defect and common atrioventricular junction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Progressive retinal dystrophy due to retinol transport defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Progressive retinal dystrophy due to retinol transport defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cardiac valvular defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cardiac valvular defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Juvenile arthritis due to defect in LA Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Juvenile arthritis due to defect in LA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Female infertility due to zona pellucida defect Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Female infertility due to zona pellucida defect phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Left ventricular obstructive tract defect (inherited effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular obstructive tract defect (inherited effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Left ventricular obstructive tract defect (maternal effect) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Left ventricular obstructive tract defect (maternal effect) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.