Gene Details



G6PC and homologs in 1 species are found in 284 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 CTD 355 Genes GS122430: rosiglitazone interacting genes (MeSH:C089730) in CTD
Expand Tier I Human GO 13 Genes GS206730: GO:0046415 urate metabolic process
Expand Tier I Human GO 27 Genes GS202197: GO:0044247 cellular polysaccharide catabolic process
Expand Tier I Human CTD 306 Genes GS126769: Calcium interacting genes (MeSH:D002118) in CTD
Expand Tier I Human GO 108 Genes GS203164: GO:0015758 glucose transport
Expand Tier I Human GO 1191 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human GO 556 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human CTD 20 Genes GS125144: 4,4'-diaminodiphenylmethane interacting genes (MeSH:C009505) in CTD
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 70 Genes GS125512: Vanadates interacting genes (MeSH:D014638) in CTD
Expand Tier I Human GO 4 Genes GS207162: GO:0015712 hexose phosphate transport
Expand Tier I Human CTD 1601 Genes GS123916: Aflatoxin B1 interacting genes (MeSH:D016604) in CTD
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human CTD 408 Genes GS123598: Paclitaxel interacting genes (MeSH:D017239) in CTD
Expand Tier I Human GO 590 Genes GS205780: GO:0044723 single-organism carbohydrate metabolic process
Expand Tier I Human GO 64 Genes GS201923: GO:0019319 hexose biosynthetic process
Expand Tier I Human 13 Genes GS175483: HP:0000991 Xanthomatosis
Expand Tier I Human 61 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 68 Genes GS199727: GO:0044042 glucan metabolic process
Expand Tier I Human GO 166 Genes GS195147: GO:0016051 carbohydrate biosynthetic process
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human GO 355 Genes GS198370: GO:0042578 phosphoric ester hydrolase activity
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human CTD 2424 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
Expand Tier I Human CTD 51 Genes GS124624: tetrabrominated diphenyl ether 47 interacting genes (MeSH:C517826) in CTD
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 17 Genes GS173339: HP:0004368 Increased purine levels
Expand Tier I Human 36 Genes GS175798: HP:0002896 Neoplasm of the liver
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human GO 29 Genes GS208136: GO:0000272 polysaccharide catabolic process
Expand Tier I Human CTD 147 Genes GS123838: cyanoginosin LR interacting genes (MeSH:C057862) in CTD
Expand Tier I Human 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human 17 Genes GS171261: HP:0002149 Hyperuricemia
Expand Tier I Human 56 Genes GS173195: HP:0012091 Abnormality of pancreas physiology
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human CTD 377 Genes GS121976: Zidovudine interacting genes (MeSH:D015215) in CTD
Expand Tier I Human GO 810 Genes GS195897: GO:0044255 cellular lipid metabolic process
Expand Tier I Human 167 Genes GS171201: HP:0001941 Acidosis
Expand Tier I Human GO 230 Genes GS194306: GO:0031300 intrinsic to organelle membrane
Expand Tier I Human CTD 133 Genes GS123377: Glucose interacting genes (MeSH:D005947) in CTD
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 89 Genes GS176345: HP:0003128 Lactic acidosis
Expand Tier I Human GO 3 Genes GS199975: GO:0004346 glucose-6-phosphatase activity
Expand Tier I Human CTD 3 Genes GS124840: bis(quercetinato)oxovanadium(IV) interacting genes (MeSH:C517295) in CTD
Expand Tier I Human 52 Genes GS171719: HP:0000787 Nephrolithiasis
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 106 Genes GS199148: GO:0030176 integral to endoplasmic reticulum membrane
Expand Tier I Human GO 104 Genes GS202606: GO:0006641 triglyceride metabolic process
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 GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human CTD 265 Genes GS125371: Cadmium Chloride interacting genes (MeSH:D019256) in CTD
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human CTD 162 Genes GS123134: Forskolin interacting genes (MeSH:D005576) in CTD
Expand Tier I Human CTD 272 Genes GS123751: Cadmium interacting genes (MeSH:D002104) in CTD
Expand Tier I Human CTD 166 Genes GS126494: epigallocatechin gallate interacting genes (MeSH:C045651) in CTD
Expand Tier I Human 24 Genes GS175065: HP:0004352 Abnormality of purine metabolism
Expand Tier I Human CTD 533 Genes GS125159: Rotenone interacting genes (MeSH:D012402) in CTD
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 281 Genes GS207421: GO:0008202 steroid metabolic process
Expand Tier I Human CTD 527 Genes GS125792: Ethanol interacting genes (MeSH:D000431) in CTD
Expand Tier I Human GO 741 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human CTD 594 Genes GS121595: Dexamethasone interacting genes (MeSH:D003907) in CTD
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 5 Genes GS126543: bis(allixinato)oxovanadium(IV) interacting genes (MeSH:C511635) in CTD
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human CTD 29 Genes GS125702: Metformin interacting genes (MeSH:D008687) in CTD
Expand Tier I Human GO 280 Genes GS207949: GO:0005996 monosaccharide metabolic process
Expand Tier I Human CTD 514 Genes GS125959: Cisplatin interacting genes (MeSH:D002945) in CTD
Expand Tier I Human GO 68 Genes GS205150: GO:0006073 cellular glucan metabolic process
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human GO 60 Genes GS210707: GO:0006094 gluconeogenesis
Expand Tier I Human CTD 238 Genes GS121381: fumonisin B1 interacting genes (MeSH:C056933) in CTD
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 53 Genes GS207467: GO:0015748 organophosphate ester transport
Expand Tier I Human GO 4 Genes GS207563: GO:0051156 glucose 6-phosphate metabolic process
Expand Tier I Human 25 Genes GS171215: HP:0000095 Morphological abnormalities of the glomeruli
Expand Tier I Human GO 57 Genes GS200993: GO:0044275 cellular carbohydrate catabolic process
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 837 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 1138 Genes GS193812: GO:0006629 lipid metabolic process
Expand Tier I Human GO 107 Genes GS194720: GO:0035264 multicellular organism growth
Expand Tier I Human 68 Genes GS175906: HP:0002910 Elevated hepatic transaminases
Expand Tier I Human GO 10 Genes GS195943: GO:0050308 sugar-phosphatase activity
Expand Tier I Human GO 109 Genes GS198223: GO:0006639 acylglycerol metabolic process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 137 Genes GS205788: GO:0044724 single-organism carbohydrate catabolic process
Expand Tier I Human GO 39 Genes GS203887: GO:1901264 carbohydrate derivative transport
Expand Tier I Human GO 110 Genes GS207466: GO:0015749 monosaccharide transport
Expand Tier III Human 224 Genes GS218958: Diff expressed in small bowel of Crohn’s-like disease of the pouch vs normal controls.
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 214 Genes GS208955: GO:0006006 glucose metabolic process
Expand Tier I Human CTD 129 Genes GS124163: Streptozocin interacting genes (MeSH:D013311) in CTD
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human GO 783 Genes GS208559: GO:0040007 growth
Expand Tier I Human 73 Genes GS171209: HP:0000093 Proteinuria
Expand Tier I Human 75 Genes GS175886: HP:0007378 Neoplasm of the gastrointestinal tract
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human CTD 151 Genes GS125182: Vitamin A interacting genes (MeSH:D014801) in CTD
Expand Tier I Human CTD 5075 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 110 Genes GS198224: GO:0006638 neutral lipid metabolic process
Expand Tier I Human 104 Genes GS171211: HP:0000091 Abnormality of the renal tubule
Expand Tier I Human GO 899 Genes GS204919: GO:0016772 transferase activity, transferring phosphorus-containing groups
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human CTD 191 Genes GS121455: pyrazole interacting genes (MeSH:C031280) in CTD
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 12 Genes GS197299: GO:0042301 phosphate ion binding
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human CTD 4 Genes GS126115: Phlorhizin interacting genes (MeSH:D010695) in CTD
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 19 Genes GS175076: HP:0001402 Hepatocellular carcinoma
Expand Tier I Human GO 1929 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 772 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 114 Genes GS175593: HP:0011015 Abnormality of blood glucose concentration
Expand Tier I Human GO 73 Genes GS197710: GO:0046364 monosaccharide biosynthetic process
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human CTD 132 Genes GS122195: Gentamicins interacting genes (MeSH:D005839) in CTD
Expand Tier I Human GO 60 Genes GS194763: GO:0042632 cholesterol homeostasis
Expand Tier I Human GO 67 Genes GS199923: GO:0005977 glycogen metabolic process
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 209 Genes GS200626: GO:0044262 cellular carbohydrate metabolic process
Expand Tier I Human GO 258 Genes GS195576: GO:0016791 phosphatase activity
Expand Tier I Human 92 Genes GS172356: HP:0003119 Abnormality of lipid metabolism
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human GO 208 Genes GS205580: GO:0031301 integral to organelle membrane
Expand Tier I Human CTD 31 Genes GS121816: Vancomycin interacting genes (MeSH:D014640) in CTD
Expand Tier I Human 12 Genes GS172301: HP:0000105 Enlarged kidneys
Expand Tier I Human GO 1180 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 919 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human GO 26 Genes GS203626: GO:0005980 glycogen catabolic process
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2353 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 60 Genes GS196578: GO:0055092 sterol homeostasis
Expand Tier I Human GO 789 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human GO 315 Genes GS201237: GO:0046486 glycerolipid metabolic process
Expand Tier I Human 34 Genes GS176240: HP:0010932 Abnormality of nucleobase metabolism
Expand Tier I Human GO 132 Genes GS203571: GO:0008643 carbohydrate transport
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human GO 10 Genes GS195949: GO:0019203 carbohydrate phosphatase activity
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human CTD 10 Genes GS126325: bis(maltolato)oxovanadium(IV) interacting genes (MeSH:C074212) in CTD
Expand Tier I Human 109 Genes GS174136: HP:0002014 Diarrhea
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 717 Genes GS204918: GO:0016773 phosphotransferase activity, alcohol group as acceptor
Expand Tier I Human GO 709 Genes GS210435: GO:0072521 purine-containing compound metabolic process
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 27 Genes GS208807: GO:0009251 glucan catabolic process
Expand Tier I Human GO 106 Genes GS203101: GO:0033500 carbohydrate homeostasis
Expand Tier I Human CTD 363 Genes GS125936: Tunicamycin interacting genes (MeSH:D014415) in CTD
Expand Tier I Human GO 3 Genes GS195944: GO:0050309 sugar-terminal-phosphatase activity
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 140 Genes GS195144: GO:0016052 carbohydrate catabolic process
Expand Tier I Human CTD 26 Genes GS123323: Sucrose interacting genes (MeSH:D013395) in CTD
Expand Tier I Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human CTD 5725 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 8 Genes GS173736: HP:0001997 Gout
Expand Tier I Human GO 168 Genes GS198505: GO:0006112 energy reserve metabolic process
Expand Tier I Human GO 890 Genes GS207863: GO:0009057 macromolecule catabolic process
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human 3 Genes GS175300: HP:0000295 Doll-like facies
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human CTD 358 Genes GS124286: Benzene interacting genes (MeSH:D001554) in CTD
Expand Tier I Human 16 Genes GS171214: HP:0000096 Glomerulosclerosis
Expand Tier I Human CTD 870 Genes GS123911: Ozone interacting genes (MeSH:D010126) in CTD
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human GO 106 Genes GS207016: GO:0042593 glucose homeostasis
Expand Tier I Human CTD 122 Genes GS124490: Fructose interacting genes (MeSH:D005632) in CTD
Expand Tier I Human 20 Genes GS173655: HP:0000823 Delayed puberty
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 28 Genes GS176822: HP:0011036 Abnormality of renal excretion
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 108 Genes GS203894: GO:0008645 hexose transport
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human CTD 117 Genes GS124346: dicyclanil interacting genes (MeSH:C121718) in CTD
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 25 Genes GS174393: HP:0001733 Pancreatitis
Expand Tier I Human 2 Genes GS176593: HP:0000120 Reduced creatinine clearance
Expand Tier I Human GO 790 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier I Human GO 971 Genes GS210163: GO:0006082 organic acid metabolic process
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 85 Genes GS209607: GO:0055088 lipid homeostasis
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human CTD 627 Genes GS122305: resveratrol interacting genes (MeSH:C059514) in CTD
Expand Tier I Human 15 Genes GS176275: HP:0001538 Protuberant abdomen
Expand Tier I Human GO 85 Genes GS210372: GO:0044264 cellular polysaccharide metabolic process
Expand Tier I Human 11 Genes GS171213: HP:0000097 Focal segmental glomerulosclerosis
Expand Tier I Human 182 Genes GS173028: HP:0004360 Abnormality of acid-base homeostasis
Expand Tier I Human 29 Genes GS175804: HP:0003270 Abdominal distention
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 4 Genes GS172858: HP:0000660 Lipemia retinalis
Expand Tier I Human 29 Genes GS171709: HP:0003077 Hyperlipidemia
Expand Tier I Human CTD 24 Genes GS122210: AICA ribonucleotide interacting genes (MeSH:C031143) in CTD
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human CTD 152 Genes GS121601: 1-Naphthylisothiocyanate interacting genes (MeSH:D015058) in CTD
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human CTD 71 Genes GS126676: Ketoconazole interacting genes (MeSH:D007654) in CTD
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 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 4 Genes GS199438: GO:0015760 glucose-6-phosphate transport
Expand Tier I Human 2 Genes GS174432: HP:0002254 Intermittent diarrhea
Expand Tier I Human CTD 25 Genes GS126204: Niacinamide interacting genes (MeSH:D009536) in CTD
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human CTD 64 Genes GS122279: Endosulfan interacting genes (MeSH:D004726) in CTD
Expand Tier I Human GO 250 Genes GS201922: GO:0019318 hexose metabolic process
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human CTD 3171 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human GO 1205 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human GO 94 Genes GS199924: GO:0005976 polysaccharide metabolic process
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 CTD 41 Genes GS125469: Bacitracin interacting genes (MeSH:D001414) in CTD
Expand Tier I Human CTD 5 Genes GS126093: Betamethasone interacting genes (MeSH:D001623) in CTD
Expand Tier I Human 105 Genes GS171199: HP:0001943 Hypoglycemia
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 123 Genes GS199200: GO:0031227 intrinsic to endoplasmic reticulum membrane
Expand Tier I Human CTD 9 Genes GS127092: tungstate interacting genes (MeSH:C045951) in CTD
Expand Tier I Human 12 Genes GS174326: HP:0003199 Decreased muscle mass
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology