Gene Details



SLC25A4 and homologs in 1 species are found in 265 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 6 Genes GS208315: GO:0015868 purine ribonucleotide transport
Expand Tier I Human GO 718 Genes GS206695: GO:0044703 multi-organism reproductive process
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Human GO 381 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human 8 Genes GS171853: HP:0000590 Progressive external ophthalmoplegia
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human GO 163 Genes GS200227: GO:0030073 insulin secretion
Expand Tier III Human 2187 Genes GS218390: Alcoholism Susceptibility Chr 1
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 691 Genes GS210096: GO:0032940 secretion by cell
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human CTD 4423 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 60 Genes GS207407: GO:0015297 antiporter activity
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Human GO 18 Genes GS203952: GO:0015813 L-glutamate transport
Expand Tier I Human GO 129 Genes GS196969: GO:0006865 amino acid transport
Expand Human 35 Genes GS219833: http://www.broadinstitute.org/gsea/msigdb/cards/REGULATION_OF_PROTEIN_MODIFICATION_PROCESS
Expand Tier I Human GO 13 Genes GS204676: GO:0043090 amino acid import
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Human GO 149 Genes GS196560: GO:0019867 outer membrane
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human CTD 866 Genes GS126764: Calcitriol interacting genes (MeSH:D002117) in CTD
Expand Tier I Human GO 152 Genes GS197456: GO:0015931 nucleobase-containing compound transport
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human CTD 200 Genes GS125369: Lamivudine interacting genes (MeSH:D019259) in CTD
Expand Tier I Human CTD 10 Genes GS124540: 10-(fluoroethoxyphosphinyl)-N-(biotinamidopentyl)decanamide interacting genes (MeSH:C403065) in CTD
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human GO 328 Genes GS208795: GO:0015980 energy derivation by oxidation of organic compounds
Expand Tier I Human 24 Genes GS171839: HP:0003458 EMG: myopathic abnormalities
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Human GO 1099 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 5 Genes GS207550: GO:0005345 purine nucleobase transmembrane transporter activity
Expand Tier I Human GO 138 Genes GS206621: GO:0050796 regulation of insulin secretion
Expand Tier I Human GO 206 Genes GS195926: GO:0042886 amide transport
Expand Tier I Human GO 184 Genes GS200226: GO:0030072 peptide hormone secretion
Expand Tier I Human GO 600 Genes GS201231: GO:0060548 negative regulation of cell death
Expand Tier I Human GO 3 Genes GS203978: GO:0051935 L-glutamate uptake involved in synaptic transmission
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 845 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human CTD 234 Genes GS125125: 2-Acetylaminofluorene interacting genes (MeSH:D015073) in CTD
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 4 Genes GS204538: GO:0015853 adenine transport
Expand Tier I Human GO 4 Genes GS194819: GO:0015867 ATP transport
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 819 Genes GS198970: GO:0031967 organelle envelope
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human GO 4283 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human GO 224 Genes GS201356: GO:0007005 mitochondrion organization
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human GO 53 Genes GS207467: GO:0015748 organophosphate ester transport
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 1218 Genes GS197008: GO:0005887 integral to plasma membrane
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 155 Genes GS202792: GO:0090087 regulation of peptide transport
Expand Tier I Human 11 Genes GS175292: HP:0003688 Decreased activity of cytochrome C oxidase in muscle tissue
Expand Tier I Human GO 1539 Genes GS196282: GO:0012501 programmed cell death
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human GO 39 Genes GS203887: GO:1901264 carbohydrate derivative transport
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 553 Genes GS201022: GO:0071705 nitrogen compound transport
Expand Tier I Human GO 199 Genes GS199724: GO:0015833 peptide transport
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 6 Genes GS208319: GO:0015865 purine nucleotide transport
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human GO 58 Genes GS200162: GO:0008637 apoptotic mitochondrial changes
Expand Human 17 Genes GS219772: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human GO 137 Genes GS201740: GO:0001505 regulation of neurotransmitter levels
Expand Tier I Human 6 Genes GS171897: HP:0011103 Abnormality of the left ventricular outflow tract
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 11 Genes GS204678: GO:0043092 L-amino acid import
Expand Tier I Human GO 183 Genes GS206896: GO:0046883 regulation of hormone secretion
Expand Human 21 Genes GS219773: http://www.broadinstitute.org/gsea/msigdb/cards/REGULATION_OF_PROTEIN_AMINO_ACID_PHOSPHORYLATION
Expand Human 17 Genes GS221377: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human GO 15 Genes GS196970: GO:0006862 nucleotide transport
Expand Tier I Human GO 2033 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 228 Genes GS200826: GO:0009914 hormone transport
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 263 Genes GS202551: GO:0015711 organic anion transport
Expand Tier I Human 48 Genes GS171444: HP:0000602 Ophthalmoplegia
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human GO 2 Genes GS199334: GO:0015207 adenine transmembrane transporter activity
Expand Tier I Human GO 133 Genes GS201349: GO:0006836 neurotransmitter transport
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 505 Genes GS198971: GO:0031966 mitochondrial membrane
Expand Tier I Human GO 153 Genes GS207353: GO:0090276 regulation of peptide hormone secretion
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 447 Genes GS209385: GO:0044403 symbiosis, encompassing mutualism through parasitism
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human GO 2 Genes GS194298: GO:0005471 ATP:ADP antiporter activity
Expand Tier I Human GO 63 Genes GS200729: GO:0006835 dicarboxylic acid transport
Expand Tier I Human GO 155 Genes GS209376: GO:0002791 regulation of peptide secretion
Expand Human 19 Genes GS219771: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHATE_METABOLIC_PROCESS
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 1929 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 188 Genes GS209375: GO:0002790 peptide secretion
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 7 Genes GS174523: HP:0009141 Depletion of mitochondrial DNA in muscle tissue
Expand Tier I Human CTD 122 Genes GS125639: Acrolein interacting genes (MeSH:D000171) in CTD
Expand Tier I Human GO 7 Genes GS196971: GO:0006863 purine nucleobase transport
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human 20 Genes GS174907: HP:0000544 External ophthalmoplegia
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 351 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 540 Genes GS196195: GO:0022415 viral reproductive process
Expand Tier I Human GO 143 Genes GS198965: GO:0031968 organelle outer membrane
Expand Tier I Human GO 311 Genes GS209586: GO:0022804 active transmembrane transporter activity
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 4 Genes GS171541: HP:0003548 Subsarcolemmal accumulations of abnormally shaped mitochondria
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human GO 222 Genes GS203929: GO:0046879 hormone secretion
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 13 Genes GS207418: GO:0015858 nucleoside transport
Expand Tier I Human GO 378 Genes GS208323: GO:0010817 regulation of hormone levels
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human GO 964 Genes GS202799: GO:0051049 regulation of transport
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human 6 Genes GS172766: HP:0001682 Subvalvular aortic stenosis
Expand Tier I Human GO 220 Genes GS200204: GO:0015849 organic acid transport
Expand Tier I Human GO 3 Genes GS203976: GO:0051933 amino acid uptake involved in synaptic transmission
Expand Tier I Human 16 Genes GS175141: HP:0003800 Muscle abnormality related to mitochondrial dysfunction
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 735 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human CTD 794 Genes GS125548: Doxorubicin interacting genes (MeSH:D004317) in CTD
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human GO 344 Genes GS209957: GO:0003001 generation of a signal involved in cell-cell signaling
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human CTD 1453 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
Expand Tier I Human GO 9 Genes GS204539: GO:0015851 nucleobase transport
Expand Human 86 Genes GS222261: Genes associated with retinitis pigmentosa (RP) on OMIM database
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 1697 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 19 Genes GS203737: GO:0015800 acidic amino acid transport
Expand Tier I Human 38 Genes GS171754: HP:0001711 Abnormality of the left ventricle
Expand Tier I Human GO 122 Genes GS197356: GO:0005741 mitochondrial outer membrane
Expand Tier I Human GO 980 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human CTD 480 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Human GO 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human CTD 127 Genes GS125370: tolcapone interacting genes (MeSH:C066340) in CTD
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human GO 369 Genes GS199224: GO:0019048 virus-host interaction
Expand Tier I Human GO 1374 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human GO 15 Genes GS207423: GO:0070265 necrotic cell death
Expand Tier I Human 14 Genes GS175579: HP:0003200 Ragged-red muscle fibers
Expand Tier I Human GO 608 Genes GS195457: GO:0060341 regulation of cellular localization
Expand Tier I Human GO 168 Genes GS198505: GO:0006112 energy reserve metabolic process
Expand Tier I Human 6 Genes GS172820: HP:0003689 Multiple mitochondrial DNA deletions
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human GO 27 Genes GS197457: GO:0015932 nucleobase-containing compound transmembrane transporter activity
Expand Tier I Human GO 793 Genes GS196790: GO:0046903 secretion
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 192 Genes GS207409: GO:0015291 secondary active transmembrane transporter activity
Expand Tier I Human GO 1324 Genes GS207293: GO:0032879 regulation of localization
Expand Tier I Human GO 439 Genes GS202796: GO:0051046 regulation of secretion
Expand Tier I Human 98 Genes GS176756: HP:0011420 Death
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human CTD 1760 Genes GS123048: Tretinoin interacting genes (MeSH:D014212) in CTD
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human GO 1086 Genes GS194481: GO:0019899 enzyme binding
Expand Tier I Human GO 313 Genes GS196355: GO:0006820 anion transport
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 11 Genes GS198513: GO:0010939 regulation of necrotic cell death
Expand Tier I Human 47 Genes GS174397: HP:0003546 Exercise intolerance
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 10 Genes GS173931: HP:0001670 Asymmetric septal hypertrophy
Expand Tier I Human GO 218 Genes GS197101: GO:0046942 carboxylic acid transport
Expand Tier I Human GO 344 Genes GS202633: GO:0023061 signal release
Expand Tier I Human 15 Genes GS172526: HP:0001699 Sudden death
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Human 20 Genes GS219759: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PROTEIN_MODIFICATION_PROCESS
Expand Tier I Human CTD 98 Genes GS126879: Toluene interacting genes (MeSH:D014050) in CTD
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 34 Genes GS171944: HP:0003324 Generalized muscle weakness
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human 58 Genes GS172853: HP:0004303 Abnormality of muscle fibers
Expand Tier I Human GO 8 Genes GS203968: GO:0051938 L-glutamate import
Expand Tier I Human GO 5 Genes GS202509: GO:0060547 negative regulation of necrotic cell death
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1522 Genes GS194172: GO:0006915 apoptotic process
Expand Tier I Human GO 694 Genes GS203305: GO:0016032 viral reproduction
Expand Tier I Human GO 5 Genes GS204783: GO:0051503 adenine nucleotide transport
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 1202 Genes GS201696: GO:0010941 regulation of cell death
Expand Tier I Human GO 411 Genes GS203490: GO:0051701 interaction with host
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 1751 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human GO 1914 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Human GO 527 Genes GS198059: GO:0005740 mitochondrial envelope
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Human 40 Genes GS219767: http://www.broadinstitute.org/gsea/msigdb/cards/REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human GO 450 Genes GS197593: GO:0006091 generation of precursor metabolites and energy
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 1972 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 14 Genes GS207990: GO:0000002 mitochondrial genome maintenance
Expand Tier I Human GO 832 Genes GS194556: GO:0031975 envelope
Expand Tier I Human CTD 3 Genes GS121849: 4-hydroxy-2-hexenal interacting genes (MeSH:C045934) in CTD
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human GO 3 Genes GS200937: GO:0015866 ADP transport
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 1262 Genes GS199199: GO:0031226 intrinsic to plasma membrane
Expand Human 17 Genes GS221128: http://www.broadinstitute.org/gsea/msigdb/cards/POSITIVE_REGULATION_OF_PHOSPHORYLATION
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human GO 29 Genes GS199624: GO:0015807 L-amino acid transport
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 22 Genes GS201739: GO:0001504 neurotransmitter uptake
Expand Tier I Human GO 651 Genes GS195082: GO:0007268 synaptic transmission
Expand Tier I Human GO 447 Genes GS196889: GO:0044419 interspecies interaction between organisms
Expand Tier I Human GO 7 Genes GS204319: GO:0015205 nucleobase transmembrane transporter activity
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD