Gene Details



SDHA and homologs in 6 species are found in 406 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 Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 112 Genes GS174327: HP:0003198 Myopathy
Expand Tier I Human GO 52 Genes GS210158: GO:0006084 acetyl-CoA metabolic process
Expand Tier I Human 64 Genes GS174310: HP:0100705 Abnormality of the glial cells
Expand Tier I Human 173 Genes GS128223: Proteins found to be modified by at least two drugs of abuse
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier I Mouse GO 1822 Genes GS190997: GO:0044281 small molecule metabolic process
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human CTD 64 Genes GS123959: Taurine interacting genes (MeSH:D013654) in CTD
Expand Tier I Human GO 159 Genes GS208404: GO:0045333 cellular respiration
Expand Tier I Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Mouse GO 361 Genes GS179795: GO:0019866 organelle inner membrane
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human GO 4 Genes GS201556: GO:0000104 succinate dehydrogenase activity
Expand Tier I Mouse 460 Genes GS135648: cocaine induced activation 11 (Cocia11, Published QTL Chr 13)
Expand Tier II Mouse 134 Genes GS34121: Cerebellum Gene expression correlates of Open Field locomotion (activity beam breaks) 45-60 min post 2nd cocaine in Males BXD
Expand Tier I Mouse GO 32 Genes GS186213: GO:0022904 respiratory electron transport chain
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human GO 26 Genes GS199767: GO:0006099 tricarboxylic acid cycle
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Mouse 463 Genes GS135228: Angiostrongylus costaricensis nematode susceptibility 2 (Acsns2, Published QTL Chr 13)
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Human 1661 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Mouse GO 195 Genes GS182519: GO:0006732 coenzyme metabolic process
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 43 Genes GS193215: GO:0006084 acetyl-CoA metabolic process
Expand Tier I Human 60 Genes GS172428: HP:0002151 Increased serum lactate
Expand Tier I Human CTD 578 Genes GS123943: Curcumin interacting genes (MeSH:D003474) in CTD
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 953 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Mouse GO 1209 Genes GS178284: GO:0031090 organelle membrane
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
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 Mouse 3319 Genes GS127931: Olfactory bulb - Allen Mouse Brain Atlas
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human GO 147 Genes GS197469: GO:0044455 mitochondrial membrane part
Expand Tier I Human 319 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Mouse GO 77 Genes GS181430: GO:0006637 acyl-CoA metabolic process
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Human GO 72 Genes GS202766: GO:0050660 flavin adenine dinucleotide binding
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
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 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 714 Genes GS182173: GO:0031967 organelle envelope
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human GO 93 Genes GS193942: GO:0035383 thioester metabolic process
Expand Tier I Mouse 2963 Genes GS127934: Retrohippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier II Mouse 39 Genes GS35096: Cerebellum Gene expression correlates of Open Field TOTAL locomotion (activity beam breaks) in Males BXD
Expand Tier II Mouse 134 Genes GS34176: Cerebellum Gene expression correlates of Open Field rears 45-60 min post 2nd cocaine in Males BXD
Expand Tier I Human 6 Genes GS175544: HP:0008972 Decreased activity of mitochondrial respiratory chain
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Mouse GO 37 Genes GS177695: GO:0051187 cofactor catabolic process
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 50 Genes GS176914: HP:0002171 Gliosis
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Human 23 Genes GS219632: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CITRATE_CYCLE_TCA_CYCLE
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 53 Genes GS173243: HP:0001336 Myoclonus
Expand Tier I Human GO 505 Genes GS198971: GO:0031966 mitochondrial membrane
Expand Tier I Human GO 8595 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 709 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human GO 351 Genes GS198058: GO:0005743 mitochondrial inner membrane
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 1518 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse 348 Genes GS136248: molar crown diameter QTL 1 (Mcdq1, Published QTL Chr 13)
Expand Tier I Human GO 4 Genes GS204477: GO:0045281 succinate dehydrogenase complex
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse DRG 2693 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier III Mouse 1964 Genes GS865: Sey_Pax6_Age_Reduced_Linear_Incr
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human GO 741 Genes GS201250: GO:0044429 mitochondrial part
Expand Tier I Mouse 456 Genes GS135668: circadian period of locomotor activity 11 (Cplaq11, Published QTL Chr 13)
Expand Human 1183 Genes GS219682: http://www.broadinstitute.org/gsea/msigdb/cards/INTRACELLULAR_ORGANELLE_PART
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 49 Genes GS174071: HP:0009125 Lipodystrophy
Expand Tier I Mouse GO 731 Genes GS193220: GO:0006082 organic acid metabolic process
Expand Tier II Mouse 13 Genes GS34295: Cerebellum Gene expression correlates of Activity in 30 second interval post 3rd tone shock pairing in Males BXD
Expand Tier I Mouse GO 22 Genes GS182966: GO:0006099 tricarboxylic acid cycle
Expand Tier I Human GO 27 Genes GS209846: GO:0046356 acetyl-CoA catabolic process
Expand Tier I Mouse 3096 Genes GS127928: Lateral septal complex - Allen Mouse Brain Atlas
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Mouse 2918 Genes GS127935: Striatum dorsal region - Allen Mouse Brain Atlas
Expand Tier I Human GO 328 Genes GS208795: GO:0015980 energy derivation by oxidation of organic compounds
Expand Tier I Human 40 Genes GS173722: HP:0002490 Increased CSF lactate
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Human CTD 1148 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier I Mouse GO 180 Genes GS185926: GO:0050662 coenzyme binding
Expand Tier I Mouse DRG 612 Genes provisional GS87381: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 43 Genes GS172180: HP:0012103 Abnormality of the mitochondrion
Expand Tier I Human CTD 1587 Genes GS124695: arsenic trioxide interacting genes (MeSH:C006632) in CTD
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse DRG 361 Genes provisional GS86497: Table S2: Additional data file 2 - Lists of probe sets of genes with expression altered by acute and chronic morphine (ANOVA; FDR < 1%). C57BL/6J [DRG]
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 33 Genes GS202498: GO:0009109 coenzyme catabolic process
Expand Tier I Human 41 Genes GS174305: HP:0000712 Emotional lability
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 3275 Genes GS199267: GO:0043234 protein complex
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
Expand Tier I Human 261 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 33 Genes GS185666: GO:0009109 coenzyme catabolic process
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 846 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Mouse 462 Genes GS135980: wound healing/regeneration 7 (Heal7, Published QTL Chr 13)
Expand Tier I Human CTD 670 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 182 Genes GS173028: HP:0004360 Abnormality of acid-base homeostasis
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Mouse 454 Genes GS135512: body weight day 30 males 2 (Bwem2, Published QTL Chr 13)
Expand Tier I Human GO 262 Genes GS202364: GO:0048037 cofactor binding
Expand Tier I Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
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 Mouse GO 4 Genes GS184750: GO:0000104 succinate dehydrogenase activity
Expand Tier I Mouse GO 232 Genes GS177696: GO:0051186 cofactor metabolic process
Expand Tier I Human GO 6769 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 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse 379 Genes GS135401: body growth late QTL 10 (Bglq10, Published QTL Chr 13)
Expand Tier I Human GO 186 Genes GS202764: GO:0050662 coenzyme binding
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Mouse GO 2263 Genes GS192174: GO:0000166 nucleotide binding
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 481 Genes GS136721: susceptibility to lung cancer 23 (Sluc23, Published QTL Chr 13)
Expand Tier I Human 34 Genes GS176898: HP:0002352 Leukoencephalopathy
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Mouse 3289 Genes GS127924: Cerebral cortex - Allen Mouse Brain Atlas
Expand Tier I Mouse 3384 Genes GS127925: Hippocampal formation - Allen Mouse Brain Atlas
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human CTD 1068 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 344 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Mouse GO 342 Genes GS181270: GO:0005743 mitochondrial inner membrane
Expand Tier I Human 89 Genes GS176345: HP:0003128 Lactic acidosis
Expand Tier I Human 195 Genes GS174813: HP:0001638 Cardiomyopathy
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse GO 23 Genes GS192900: GO:0046356 acetyl-CoA catabolic process
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Mouse DRG 1187 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier II Mouse 463 Genes GS83966: cocaine induced activation 11 (Cocia11, Published QTL, Chr 13, MGI:3040202)
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Mouse GO 55 Genes GS177317: GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 3211 Genes GS192509: GO:0006810 transport
Expand Tier I Human 6 Genes GS175167: HP:0011922 Abnormal activity of mitochondrial respiratory chain
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Human 346 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier II Mouse 18 Genes GS34454: Cerebellum Gene expression correlates of Novel environment locomotion (activity beam breaks) 15-30 min in the periphery in Females BXD
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse 355 Genes GS136128: listeriosis resistance 2 (Listr2, Published QTL Chr 13)
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Mouse 454 Genes GS136967: Y-linked autoimmune acceleration QTL 1 (Yaa1, Published QTL Chr 13)
Expand Tier I Human 36 Genes GS174658: HP:0001427 Mitochondrial inheritance
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 48 Genes GS171444: HP:0000602 Ophthalmoplegia
Expand Tier I Human 626 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 Mouse GO 2263 Genes GS187023: GO:1901265 nucleoside phosphate binding
Expand Tier I Mouse DRG 2537 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Human 55 Genes GS172097: HP:0000580 Pigmentary retinopathy
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 148 Genes GS203053: GO:0022900 electron transport chain
Expand Tier I Rat DRG 4920 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 37 Genes GS170996: HP:0007305 CNS demyelination
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Mouse 413 Genes GS136489: primordial germ cell tumor locus 1 (Pgct1, Published QTL Chr 13)
Expand Tier I Human GO 76 Genes GS204180: GO:0070469 respiratory chain
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Mouse 379 Genes GS136681: skull morphology 20 (Skull20, Published QTL Chr 13)
Expand Tier I Human GO 4 Genes GS207058: GO:0045283 fumarate reductase complex
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse GO 10 Genes GS178159: GO:0006105 succinate metabolic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 78 Genes GS191477: GO:0045333 cellular respiration
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human CTD 18 Genes GS123977: 2,6-dichloro-4-nitrophenol interacting genes (MeSH:C015802) in CTD
Expand Tier I Mouse 330 Genes GS136746: spermatogenesis defect 4 (Spmd4, Published QTL Chr 13)
Expand Tier I Mouse GO 482 Genes GS181271: GO:0005740 mitochondrial envelope
Expand Tier I Human CTD 127 Genes GS125370: tolcapone interacting genes (MeSH:C066340) in CTD
Expand Tier II Mouse 25 Genes GS33965: Cerebellum Gene expression correlates of Morphine distance (cm) travelled minutes 165-180 in Females BXD
Expand Tier I Mouse 463 Genes GS136487: predicted fat percentage 3 (Pfat3, Published QTL Chr 13)
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 14 Genes GS175579: HP:0003200 Ragged-red muscle fibers
Expand Tier I Human 200 Genes GS174812: HP:0001637 Abnormality of the myocardium
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse 379 Genes GS135451: bone length and organs 7 (Bod7, Published QTL Chr 13)
Expand Tier I Human GO 4 Genes GS208854: GO:0045273 respiratory chain complex II
Expand Tier I Human GO 257 Genes GS194434: GO:0051186 cofactor metabolic process
Expand Tier I Mouse 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Mouse 3329 Genes GS127933: Pons - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 3268 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Mouse GO 1648 Genes GS190954: GO:0009056 catabolic process
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse 402 Genes GS135747: experimental allergic encephalomyelitis susceptibility 13 (Eae13, Published QTL Chr 13)
Expand Tier I Human GO 381 Genes GS196559: GO:0019866 organelle inner membrane
Expand Tier I Mouse GO 77 Genes GS177219: GO:0035383 thioester metabolic process
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human GO 7638 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 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse 426 Genes GS136125: lipoprotein QTL 2 (Lipq2, Published QTL Chr 13)
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse 348 Genes GS135348: Avp transcript abundance QTL 3 (Avptaq3, Published QTL Chr 13)
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 114 Genes GS186210: GO:0022900 electron transport chain
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 42 Genes GS172398: HP:0003287 Abnormality of mitochondrial metabolism
Expand Tier I Mouse GO 292 Genes GS180799: GO:0006091 generation of precursor metabolites and energy
Expand Tier I Mouse 484 Genes GS129182: spontaneous crescentic glomerulonephritis QTL 5 (Scgq5 Published QTL Chr 13)
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Mouse DRG 612 Genes provisional GS86911: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by morphine treatment (661). [DRG]
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse 3109 Genes GS127923: Cerebellum - Allen Mouse Brain Atlas
Expand Tier I Mouse 453 Genes GS135682: Crh transcript abundance QTL 3 (Crhtaq3, Published QTL Chr 13)
Expand Tier I Human GO 55 Genes GS194047: GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
Expand Tier I Mouse 348 Genes GS135734: delta power in slow-wave sleep 1 (Dps1, Published QTL Chr 13)
Expand Tier I Human GO 2 Genes GS205027: GO:0008177 succinate dehydrogenase (ubiquinone) activity
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 44 Genes GS204135: GO:0009060 aerobic respiration
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Mouse GO 735 Genes GS181962: GO:0016491 oxidoreductase activity
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Rat DRG 4920 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 120 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Mouse GO 717 Genes GS185724: GO:0043436 oxoacid metabolic process
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier II Mouse 407 Genes GS84269: ethanol withdrawal (Published QTL, Chr 13)
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 459 Genes GS182174: GO:0031966 mitochondrial membrane
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse 379 Genes GS136652: skeletal size (tail length) 6 (Skl6, Published QTL Chr 13)
Expand Tier I Human 84 Genes GS174760: HP:0002376 Developmental regression
Expand Tier I Human CTD 213 Genes GS125842: Ascorbic Acid interacting genes (MeSH:D001205) in CTD
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse 402 Genes GS136271: modifier of obesity 2 (Mobe2, Published QTL Chr 13)
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human CTD 480 Genes GS122634: Ketone Bodies interacting genes (MeSH:D007657) in CTD
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse GO 1518 Genes GS192074: GO:1901575 organic substance catabolic process
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 110 Genes GS203056: GO:0022904 respiratory electron transport chain
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 47 Genes GS174397: HP:0003546 Exercise intolerance
Expand Tier I Human 2 Genes GS171373: HP:0004897 Stress/infection-induced lactic acidosis
Expand Tier I Human 58 Genes GS172853: HP:0004303 Abnormality of muscle fibers
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Mouse 348 Genes GS135776: epistatic circling C C57L/J 2 (Eclc, Published QTL Chr 13)
Expand Tier I Human 2 Genes GS175646: HP:0006980 Leukoencephalopathy, progressive
Expand Tier I Mouse 3136 Genes GS127926: Hippocampal region - Allen Mouse Brain Atlas
Expand Tier I Human GO 527 Genes GS198059: GO:0005740 mitochondrial envelope
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human 62 Genes GS171488: HP:0002921 Abnormality of the cerebrospinal fluid
Expand Tier I Mouse GO 4 Genes GS186159: GO:0016635 oxidoreductase activity, acting on the CH-CH group of donors, quinone or related compound as acceptor
Expand Tier I Human GO 450 Genes GS197593: GO:0006091 generation of precursor metabolites and energy
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 832 Genes GS194556: GO:0031975 envelope
Expand Tier I Mouse GO 2 Genes GS188168: GO:0008177 succinate dehydrogenase (ubiquinone) activity
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human CTD 476 Genes GS125040: Thioacetamide interacting genes (MeSH:D013853) in CTD
Expand Tier I Mouse GO 147 Genes GS191854: GO:0015980 energy derivation by oxidation of organic compounds
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse 444 Genes GS136426: pulmonary adenoma susceptibility 10 (Pas10, Published QTL Chr 13)
Expand Tier I Mouse GO 726 Genes GS177814: GO:0031975 envelope
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier I Mouse GO 590 Genes GS184446: GO:0044429 mitochondrial part
Expand Tier I Mouse 481 Genes GS135943: HDL cholesterol level 2 (Hdlcl2, Published QTL Chr 13)
Expand Tier I Human 44 Genes GS171924: HP:0100578 Lipoatrophy
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse 454 Genes GS135666: "cerebellum pattern fissures, declival 5" (Cpfd5, Published QTL Chr 13)
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 215 Genes GS199314: GO:0006732 coenzyme metabolic process
Expand Tier I Human 106 Genes GS173246: HP:0001332 Dystonia
Expand Tier I Mouse 348 Genes GS135981: wound healing/regeneration 8 (Heal8, Published QTL Chr 13)
Expand Tier I Mouse GO 254 Genes GS185538: GO:0048037 cofactor binding
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Human 1985 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Human 334 Genes GS219678: http://www.broadinstitute.org/gsea/msigdb/cards/MITOCHONDRION
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse GO 675 Genes GS187462: GO:0019752 carboxylic acid metabolic process
Expand Tier I Mouse 3395 Genes GS127929: Medulla - Allen Mouse Brain Atlas
Expand Tier I Mouse GO 1603 Genes GS177409: GO:0005739 mitochondrion
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Human 161 Genes GS176803: HP:0001260 Dysarthria
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 4 Genes GS201364: GO:0045257 succinate dehydrogenase complex (ubiquinone)
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 2 Genes GS171496: HP:0008314 Decreased activity of mitochondrial complex II
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 68 Genes GS185928: GO:0050660 flavin adenine dinucleotide binding
Expand Tier I Human GO 69 Genes GS197357: GO:0005746 mitochondrial respiratory chain
Expand Tier I Mouse 456 Genes GS135573: cystic fibrosis body weight 5 (Cfbw5, Published QTL Chr 13)
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Human 1188 Genes GS219681: http://www.broadinstitute.org/gsea/msigdb/cards/ORGANELLE_PART
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 50 Genes GS176834: HP:0002793 Abnormal respiratory patterns
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 215 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
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 160 Genes GS174814: HP:0001639 Hypertrophic cardiomyopathy
Expand Tier I Human 378 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Mouse GO 69 Genes GS182762: GO:0043648 dicarboxylic acid metabolic process
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 18 Genes GS173560: HP:0008316 Abnormal mitochondria in muscle tissue
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 819 Genes GS198970: GO:0031967 organelle envelope
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Mouse 481 Genes GS136028: hyperinsulinemia (Hypism, Published QTL Chr 13)
Expand Tier I Human 74 Genes GS174070: HP:0009124 Abnormality of adipose tissue
Expand Tier II Mouse 62 Genes GS35202: Cerebellum Gene expression correlates of Open Field - Total horizontal distance (cm) 0-15 min post saline in Males BXD
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Human 316 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 84 Genes GS170815: HP:0011400 Abnormal CNS myelination
Expand Tier I Human 110 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Human CTD 202 Genes GS126906: sodium arsenate interacting genes (MeSH:C009277) in CTD
Expand Tier I Mouse 417 Genes GS135427: bone mechanical trait 6 (Bmch6, Published QTL Chr 13)
Expand Tier III Human 2403 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Mouse GO 1395 Genes GS185366: GO:0044248 cellular catabolic process
Expand Tier I Mouse GO 32 Genes GS187277: GO:0009060 aerobic respiration
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Mouse 379 Genes GS136222: mandible length 14 (Manln14, Published QTL Chr 13)
Expand Tier I Mouse 417 Genes GS135529: castaneus 10 week body weight 4 (C10bw4, Published QTL Chr 13)