Gene Details



SDHA and homologs in 1 species are found in 250 GeneSets:


- Entrez   - GeneNetwork   - 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 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human GO 739 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Human GO 52 Genes GS210158: GO:0006084 acetyl-CoA metabolic process
Expand Tier I Human GO 380 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Human GO 555 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 64 Genes GS174310: HP:0100705 Abnormality of the glial cells
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 71 Genes GS170917: HP:0100852 Abnormal fear/anxiety-related behavior
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 152 Genes GS128223: Proteins found to be modified by at least two drugs of abuse
Expand Tier I Human 95 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 49 Genes GS174071: HP:0009125 Lipodystrophy
Expand Tier I Human 50 Genes GS176834: HP:0002793 Abnormal respiratory patterns
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human CTD 1069 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Human CTD 64 Genes GS123959: Taurine interacting genes (MeSH:D013654) in CTD
Expand Tier I Human GO 93 Genes GS193942: GO:0035383 thioester metabolic process
Expand Tier I Human 42 Genes GS172398: HP:0003287 Abnormality of mitochondrial metabolism
Expand Tier I Human GO 27 Genes GS209846: GO:0046356 acetyl-CoA catabolic process
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 159 Genes GS208404: GO:0045333 cellular respiration
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human CTD 2422 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 39 Genes GS194433: GO:0051187 cofactor catabolic process
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 830 Genes GS194556: GO:0031975 envelope
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Human 158 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 328 Genes GS208795: GO:0015980 energy derivation by oxidation of organic compounds
Expand Tier I Human 89 Genes GS176345: HP:0003128 Lactic acidosis
Expand Tier I Human 193 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Human 6 Genes GS175544: HP:0008972 Decreased activity of mitochondrial respiratory chain
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 55 Genes GS194047: GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 40 Genes GS173722: HP:0002490 Increased CSF lactate
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human CTD 478 Genes GS125040: Thioacetamide interacting genes (MeSH:D013853) in CTD
Expand Tier I Human GO 2411 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 2 Genes GS205027: GO:0008177 succinate dehydrogenase (ubiquinone) activity
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human GO 44 Genes GS204135: GO:0009060 aerobic respiration
Expand Tier I Human 282 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human GO 4 Genes GS201556: GO:0000104 succinate dehydrogenase activity
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Human 262 Genes GS219934: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Human 18 Genes GS173560: HP:0008316 Abnormal mitochondria in muscle tissue
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 43 Genes GS172180: HP:0012103 Abnormality of the mitochondrion
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 44 Genes GS171924: HP:0100578 Lipoatrophy
Expand Tier I Human GO 1669 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human CTD 1593 Genes GS124695: arsenic trioxide interacting genes (MeSH:C006632) in CTD
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human 6 Genes GS175167: HP:0011922 Abnormal activity of mitochondrial respiratory chain
Expand Tier I Human GO 817 Genes GS198970: GO:0031967 organelle envelope
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 50 Genes GS176914: HP:0002171 Gliosis
Expand Tier I Human 118 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 153 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human GO 215 Genes GS199314: GO:0006732 coenzyme metabolic process
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 36 Genes GS174658: HP:0001427 Mitochondrial inheritance
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 74 Genes GS174070: HP:0009124 Abnormality of adipose tissue
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human GO 33 Genes GS202498: GO:0009109 coenzyme catabolic process
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 41 Genes GS174305: HP:0000712 Emotional lability
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human 48 Genes GS171444: HP:0000602 Ophthalmoplegia
Expand Tier I Human 53 Genes GS173243: HP:0001336 Myoclonus
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human GO 26 Genes GS199767: GO:0006099 tricarboxylic acid cycle
Expand Tier I Human GO 503 Genes GS198971: GO:0031966 mitochondrial membrane
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 82 Genes GS199560: GO:0043648 dicarboxylic acid metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 282 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human GO 706 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human CTD 214 Genes GS125842: Ascorbic Acid interacting genes (MeSH:D001205) in CTD
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 55 Genes GS172097: HP:0000580 Pigmentary retinopathy
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 147 Genes GS203053: GO:0022900 electron transport chain
Expand Tier I Human 102 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human 112 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 350 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 37 Genes GS170996: HP:0007305 CNS demyelination
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human GO 76 Genes GS204180: GO:0070469 respiratory chain
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2486 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 60 Genes GS172428: HP:0002151 Increased serum lactate
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 845 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Human 474 Genes GS219938: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human CTD 577 Genes GS123943: Curcumin interacting genes (MeSH:D003474) in CTD
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 1994 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 4 Genes GS207058: GO:0045283 fumarate reductase complex
Expand Tier I Human GO 2410 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human 84 Genes GS170815: HP:0011400 Abnormal CNS myelination
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human 108 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 4 Genes GS201364: GO:0045257 succinate dehydrogenase complex (ubiquinone)
Expand Tier I Human CTD 18 Genes GS123977: 2,6-dichloro-4-nitrophenol interacting genes (MeSH:C015802) in CTD
Expand Tier I Human CTD 481 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human CTD 127 Genes GS125370: tolcapone interacting genes (MeSH:C066340) in CTD
Expand Tier I Human CTD 202 Genes GS126906: sodium arsenate interacting genes (MeSH:C009277) in CTD
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Human 360 Genes GS219927: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 14 Genes GS175579: HP:0003200 Ragged-red muscle fibers
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 2361 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 4 Genes GS204477: GO:0045281 succinate dehydrogenase complex
Expand Tier I Human 2 Genes GS171496: HP:0008314 Decreased activity of mitochondrial complex II
Expand Tier I Human GO 110 Genes GS203056: GO:0022904 respiratory electron transport chain
Expand Tier I Human GO 4 Genes GS208854: GO:0045273 respiratory chain complex II
Expand Tier I Human CTD 671 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier III Human 2273 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 47 Genes GS174397: HP:0003546 Exercise intolerance
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human GO 970 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 2 Genes GS171373: HP:0004897 Stress/infection-induced lactic acidosis
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 4 Genes GS202997: GO:0016635 oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Human 360 Genes GS219710: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human 182 Genes GS173028: HP:0004360 Abnormality of acid-base homeostasis
Expand Tier I Human GO 69 Genes GS197357: GO:0005746 mitochondrial respiratory chain
Expand Tier I Human 58 Genes GS172853: HP:0004303 Abnormality of muscle fibers
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human GO 147 Genes GS197469: GO:0044455 mitochondrial membrane part
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Human 262 Genes GS219717: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_SPACE
Expand Tier I Human GO 262 Genes GS202364: GO:0048037 cofactor binding
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human GO 10 Genes GS194909: GO:0006105 succinate metabolic process
Expand Tier I Human GO 4 Genes GS198078: GO:0005749 mitochondrial respiratory chain complex II
Expand Tier I Human GO 72 Genes GS202766: GO:0050660 flavin adenine dinucleotide binding
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 2 Genes GS175646: HP:0006980 Leukoencephalopathy, progressive
Expand Tier I Human GO 186 Genes GS202764: GO:0050662 coenzyme binding
Expand Tier I Human GO 93 Genes GS198220: GO:0006637 acyl-CoA metabolic process
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 525 Genes GS198059: GO:0005740 mitochondrial envelope
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 34 Genes GS176898: HP:0002352 Leukoencephalopathy
Expand Tier I Human GO 2509 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 62 Genes GS171488: HP:0002921 Abnormality of the cerebrospinal fluid
Expand Tier I Human GO 449 Genes GS197593: GO:0006091 generation of precursor metabolites and energy
Expand Human 474 Genes GS219721: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm