Gene Details



OPA3 and homologs in 5 species are found in 506 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 MP 1087 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7747 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse 194 Genes GS227419: MSigDB Geneset - GSE27786_LSK_VS_LIN_NEG_CELL_UP
Expand Tier II Human 6197 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier I Human 258 Genes GS227508: MSigDB Geneset - V$OCT1_01
Expand Tier II Human 8283 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Mouse MP 1081 Genes GS166412: MP:0002118 abnormal lipid homeostasis
Expand Tier I Mouse MP 1190 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 350 Genes GS168129: MP:0010025 decreased total body fat amount
Expand Tier I Mouse MP 743 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier II Mouse 969 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Human 185 Genes GS228412: MSigDB Geneset - PRC2_SUZ12_UP.V1_DN
Expand Tier I Mouse MP 292 Genes GS167813: MP:0000163 abnormal cartilage morphology
Expand Tier I Human GO 7611 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse MP 187 Genes GS170738: MP:0001056 abnormal cranial nerve morphology
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Human 830 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse 200 Genes GS228984: MSigDB Geneset - GSE7852_TREG_VS_TCONV_FAT_UP
Expand Tier I Mouse MP 37 Genes GS162848: MP:0000005 increased brown adipose tissue amount
Expand Tier I Mouse MP 58 Genes GS163229: MP:0008831 abnormal insulin-like growth factor I level
Expand Tier II Human 5070 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Human 235 Genes GS229232: MSigDB Geneset - V$HFH1_01
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Human 2208 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier I Mouse GO 8629 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 112 Genes GS167702: MP:0003141 cardiac fibrosis
Expand Tier II Human 8948 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 6611 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Mouse 193 Genes GS229556: MSigDB Geneset - GSE17721_CTRL_VS_GARDIQUIMOD_1H_BMDM_DN
Expand Tier I Mouse GO 8649 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier II Mouse 1020 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier I Mouse MP 3142 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Mouse MP 381 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier II Mouse 649 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse MP 72 Genes GS169907: MP:0002090 abnormal vision
Expand Tier I Mouse MP 98 Genes GS169978: MP:0006035 abnormal mitochondrion morphology
Expand Tier I Human CTD 4474 Genes GS123265: Estradiol interacting with Oryzias latipes associated genes (MeSH:D004958) in CTD
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Human 244 Genes GS230204: MSigDB Geneset - V$T3R_Q6
Expand Tier II Human 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier III Human 2680 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier II Human 153 Genes GS238669: [MeSH] Amino Acid Metabolism, Inborn Errors : D000592
Expand Tier I Mouse MP 340 Genes GS165308: MP:0004848 abnormal liver size
Expand Tier I Mouse 193 Genes GS230568: MSigDB Geneset - GSE17721_CTRL_VS_POLYIC_4H_BMDM_UP
Expand Tier II Human 4602 Genes GS243358: [MeSH] Protein Transport : D021381
Expand Tier I Mouse GO 22753 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Human 2992 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier II Human 5190 Genes GS236912: [MeSH] Biological Transport : D001692
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 81 Genes GS235593: [MeSH] Optic Nerve Diseases : D009901
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier II Human 5301 Genes GS243658: [MeSH] Recombinant Fusion Proteins : D011993
Expand Tier II Mouse 954 Genes GS136745: spermatogenesis defect 3 (Spmd3, Published QTL Chr 7)
Expand Tier I Human 1207 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier II Human 34 Genes GS236121: [MeSH] Glutarates : D005977
Expand Tier I Mouse MP 1391 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
Expand Tier I Human 263 Genes GS232688: PC Geneset - "V$OCT1_Q5_01" pathway genes
Expand Tier I Human 235 Genes GS230791: MSigDB Geneset - V$FOXO1_01
Expand Tier II Human 11234 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Human CTD 1798 Genes GS251956: C646 compound interacting with Homo sapiens associated genes (MeSH:C584509) in CTD
Expand Tier I Mouse MP 219 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Mouse MP 96 Genes GS163468: MP:0010499 abnormal ventricle myocardium morphology
Expand Tier I Mouse MP 2295 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human 746 Genes GS228578: MSigDB Geneset - MGGAAGTG_V$GABP_B
Expand Tier II Human 1028 Genes GS237329: [MeSH] Acids, Acyclic : D000144
Expand Tier I Human 231 Genes GS232076: PC Geneset - "V$HFH1_01" pathway genes
Expand Tier II Human 3757 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Mouse MP 395 Genes GS169228: MP:0001406 abnormal gait
Expand Tier I Human 265 Genes GS228761: MSigDB Geneset - V$OCT1_Q5_01
Expand Tier I Mouse GO 13184 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 186 Genes GS227917: MSigDB Geneset - GSE37416_CTRL_VS_12H_F_TULARENSIS_LVS_NEUTROPHIL_DN
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse MP 4 Genes GS169313: MP:0011015 decreased body surface temperature
Expand Tier I Human GO 12166 Genes GS201251: GO:0044424 intracellular part
Expand Tier II Human 574 Genes GS239294: [MeSH] Heredodegenerative Disorders, Nervous System : D020271
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse MP 146 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier II Human 129 Genes GS239238: [MeSH] Lens Diseases : D007905
Expand Tier I Mouse MP 1091 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 66 Genes GS163652: MP:0001778 abnormal brown adipose tissue amount
Expand Tier I Mouse MP 58 Genes GS164195: MP:0003662 abnormal long bone epiphyseal plate proliferative zone
Expand Tier I Mouse MP 162 Genes GS169478: MP:0006395 abnormal epiphyseal plate morphology
Expand Tier I Human 124 Genes GS227776: MSigDB Geneset - V$GRE_C
Expand Tier II Human 7063 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier I Human 230 Genes GS232392: PC Geneset - "V$ZF5_B" pathway genes
Expand Tier I Human 1971 Genes GS232341: PC Geneset - "TTGTTT_V$FOXO4_01" pathway genes
Expand Tier II Mouse 969 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier I Human CTD 3845 Genes GS126898: Methyl Methanesulfonate interacting with Homo sapiens associated genes (MeSH:D008741) in CTD
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Mouse MP 112 Genes GS163679: MP:0002971 abnormal brown adipose tissue morphology
Expand Tier I Human 228 Genes GS232673: PC Geneset - "V$FOXO1_01" pathway genes
Expand Tier I Mouse MP 47 Genes GS167462: MP:0002795 dilated cardiomyopathy
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse MP 778 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Mouse 827 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier II Human 119 Genes GS235348: [MeSH] Cataract : D002386
Expand Tier I Mouse MP 866 Genes GS167025: MP:0003953 abnormal hormone level
Expand Tier I Mouse MP 260 Genes GS169191: MP:0000281 abnormal interventricular septum morphology
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Mouse MP 614 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Mouse MP 617 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Human 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier I Mouse MP 349 Genes GS165595: MP:0010545 abnormal heart layer morphology
Expand Tier II Human 3848 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier I Human 733 Genes GS232218: PC Geneset - "MGGAAGTG_V$GABP_B" pathway genes
Expand Tier I Human 2850 Genes GS232583: PC Geneset - "GGGCGGR_V$SP1_Q6" pathway genes
Expand Tier I Mouse MP 1894 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Mouse CTD 6607 Genes GS257260: Vehicle Emissions interacting with Mus musculus associated genes (MeSH:D001335) in CTD
Expand Tier II Human 119 Genes GS234779: [MeSH] Mitochondrial Diseases : D028361
Expand Tier I Mouse MP 51 Genes GS170064: MP:0004777 abnormal phospholipid level
Expand Tier II Human 142 Genes GS239635: [MeSH] Cranial Nerve Diseases : D003389
Expand Tier II Human 3976 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier I Mouse MP 273 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Mouse CTD 509 Genes GS255844: Ketolides interacting with Mus musculus associated genes (MeSH:D048628) in CTD
Expand Tier I Mouse MP 188 Genes GS168056: MP:0002628 hepatic steatosis
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Mouse 581 Genes GS136233: mandible length 7 (Manln7, Published QTL Chr 7)
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Mouse MP 335 Genes GS168497: MP:0001256 abnormal body length
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 10126 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 3924 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Mouse MP 103 Genes GS165263: MP:0005535 abnormal body temperature
Expand Tier II Human 2605 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier II Mouse 980 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Mouse MP 10 Genes GS167310: MP:0008513 thin retinal inner plexiform layer
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse MP 2000 Genes GS168476: MP:0005451 abnormal body composition
Expand Tier II Human 11248 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier II Human 6703 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Mouse MP 569 Genes GS168826: MP:0005294 abnormal heart ventricle morphology
Expand Tier I Human 256 Genes GS227818: MSigDB Geneset - V$OCT_Q6
Expand Tier I Human GO 5627 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9739 Genes GS186744: GO:0043226 organelle
Expand Tier I Human 184 Genes GS229287: MSigDB Geneset - GSE37416_CTRL_VS_6H_F_TULARENSIS_LVS_NEUTROPHIL_DN
Expand Tier I Mouse MP 3256 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 11363 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human 1989 Genes GS228205: MSigDB Geneset - TTGTTT_V$FOXO4_01
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Mouse MP 92 Genes GS165074: MP:0010563 increased heart right ventricle size
Expand Tier I Mouse MP 10 Genes GS169901: MP:0008507 thin retinal ganglion layer
Expand Tier I Mouse MP 786 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human GO 9089 Genes GS194133: GO:0005737 cytoplasm
Expand Tier II Mouse 1019 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Mouse MP 39 Genes GS170015: MP:0005608 cardiac interstitial fibrosis
Expand Tier I Mouse MP 1060 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier I Mouse GO 22332 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier I Mouse MP 1030 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10565 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier II Human 18556 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Mouse MP 164 Genes GS167797: MP:0008772 increased heart ventricle size
Expand Tier I Mouse MP 834 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier II Human 229 Genes GS240378: [MeSH] Carbazoles : D002227
Expand Tier II Human 7025 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse MP 73 Genes GS167896: MP:0009355 increased liver triglyceride level
Expand Tier II Human 7440 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Mouse 193 Genes GS229017: MSigDB Geneset - GSE11924_TFH_VS_TH2_CD4_TCELL_UP
Expand Tier I Zebrafish CTD 683 Genes GS261979: retinylamine interacting with Danio rerio associated genes (MeSH:C009167) in CTD
Expand Tier I Mouse MP 648 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier II Human 15970 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Mouse MP 86 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Mouse MP 394 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse MP 697 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier II Mouse 906 Genes GS135938: HDL level 38 (Hdl38, Published QTL Chr 7)
Expand Tier I Mouse MP 289 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier II Mouse 906 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier I Human 801 Genes GS228126: MSigDB Geneset - chr19q13
Expand Tier I Mouse MP 2915 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 2330 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Human 13379 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Mouse MP 59 Genes GS164236: MP:0008056 abnormal retinal ganglion cell morphology
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier II Human 25 Genes GS243691: [MeSH] Optic Atrophies, Hereditary : D015418
Expand Tier I Mouse MP 241 Genes GS167907: MP:0003921 abnormal heart left ventricle morphology
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse MP 1562 Genes GS165386: MP:0001262 decreased body weight
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 148 Genes GS164394: MP:0003055 abnormal long bone epiphyseal plate morphology
Expand Tier I Mouse MP 23 Genes GS163522: MP:0006309 decreased retinal ganglion cell number
Expand Tier I Mouse 986 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier II Human 728 Genes GS241409: [MeSH] Heterocyclic Compounds, 3-Ring : D006575
Expand Tier I Mouse MP 1027 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier I Mouse MP 1254 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 7446 Genes GS239443: [MeSH] RNA Splicing : D012326
Expand Tier II Mouse 969 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 127 Genes GS232073: PC Geneset - "V$GRE_C" pathway genes
Expand Tier II Human 679 Genes GS243748: [MeSH] Metabolism, Inborn Errors : D008661
Expand Tier II Human 11557 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier I Mouse MP 2315 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Mouse MP 49 Genes GS169661: MP:0004701 decreased circulating insulin-like growth factor I level
Expand Tier I Mouse MP 1471 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 196 Genes GS232279: PC Geneset - "V$HFH8_01" pathway genes
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 848 Genes GS163103: MP:0000003 abnormal adipose tissue morphology
Expand Tier I Mouse MP 889 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Mouse MP 94 Genes GS169625: MP:0005437 abnormal glycogen level
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier II Human 2389 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 246 Genes GS228135: MSigDB Geneset - V$P53_DECAMER_Q2
Expand Tier I Mouse MP 66 Genes GS168439: MP:0005534 decreased body temperature
Expand Tier I Human 255 Genes GS232070: PC Geneset - "V$OCT1_01" pathway genes
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 91 Genes GS166899: MP:0001330 abnormal optic nerve morphology
Expand Tier I Human 511 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5884 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 106 Genes GS169054: MP:0005438 abnormal glycogen homeostasis
Expand Tier I Mouse MP 1557 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Mouse MP 640 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse MP 14 Genes GS163514: MP:0006303 abnormal retinal nerve fiber layer morphology
Expand Tier II Human 3239 Genes GS240584: [MeSH] Green Fluorescent Proteins : D049452
Expand Tier II Human 14403 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Mouse 196 Genes GS227103: MSigDB Geneset - GSE17721_CTRL_VS_LPS_2H_BMDM_DN
Expand Tier II Human 266 Genes GS244540: [MeSH] Lod Score : D008126
Expand Tier I Human 195 Genes GS227316: MSigDB Geneset - GSE24634_IL4_VS_CTRL_TREATED_NAIVE_CD4_TCELL_DAY10_UP
Expand Tier I Mouse MP 393 Genes GS169957: MP:0001402 hypoactivity
Expand Tier II Human 1555 Genes GS243535: [MeSH] Neurodegenerative Diseases : D019636
Expand Tier I Mouse 195 Genes GS228241: MSigDB Geneset - GSE10239_NAIVE_VS_DAY4.5_EFF_CD8_TCELL_DN
Expand Tier I Mouse MP 3847 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Human 259 Genes GS230730: MSigDB Geneset - V$OCT_C
Expand Tier I Zebrafish CTD 98 Genes GS261580: Zinc interacting with Danio rerio associated genes (MeSH:D015032) in CTD
Expand Tier I Mouse MP 4704 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier II Human 199 Genes GS238561: [MeSH] Dicarboxylic Acids : D003998
Expand Tier II Human 14645 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Mouse 936 Genes GS135417: beta-carboline induced seizures 4 (Bis4, Published QTL Chr 7)
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Human 183 Genes GS232243: PC Geneset - "V$FREAC7_01" pathway genes
Expand Tier II Human 5620 Genes GS244452: [MeSH] Organ Specificity : D009928
Expand Tier II Human 12777 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Human 185 Genes GS228580: MSigDB Geneset - PRC2_EZH2_UP.V1_DN
Expand Tier II Human 15903 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier II Human 7201 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Mouse MP 909 Genes GS165869: MP:0002138 abnormal hepatobiliary system morphology
Expand Tier I Mouse MP 2874 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 309 Genes GS163197: MP:0006113 abnormal heart septum morphology
Expand Tier I Mouse MP 647 Genes GS164770: MP:0009250 abnormal appendicular skeleton morphology
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Mouse MP 1026 Genes GS169225: MP:0000358 abnormal cell morphology
Expand Tier I Human 87 Genes GS229015: MSigDB Geneset - SNACANNNYSYAGA_UNKNOWN
Expand Tier I Mouse MP 864 Genes GS165539: MP:0005375 adipose tissue phenotype
Expand Tier I Mouse MP 735 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse MP 55 Genes GS168793: MP:0005439 decreased glycogen level
Expand Tier II Mouse 637 Genes GS136214: lupus BXSB x NZW 6 (Lxw6, Published QTL Chr 7)
Expand Tier I Mouse GO 1603 Genes GS177409: GO:0005739 mitochondrion
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human CTD 1353 Genes GS125058: Selenium Compounds interacting with Homo sapiens associated genes (MeSH:D018036) in CTD
Expand Tier I Mouse CTD 1930 Genes GS260306: bisphenol A interacting with Mus musculus associated genes (MeSH:C006780) in CTD
Expand Tier I Human 243 Genes GS232206: PC Geneset - "V$P53_DECAMER_Q2" pathway genes
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Mouse MP 12 Genes GS166008: MP:0001492 abnormal pilomotor reflex
Expand Tier I Mouse MP 76 Genes GS169367: MP:0005405 axon degeneration
Expand Tier II Human 166 Genes GS240862: [MeSH] Staurosporine : D019311
Expand Tier II Human 11230 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Mouse MP 211 Genes GS167228: MP:0005317 increased triglyceride level
Expand Tier II Human 3173 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier II Human 14014 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier I Zebrafish CTD 2626 Genes GS261991: bisphenol A interacting with Danio rerio associated genes (MeSH:C006780) in CTD
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse MP 3960 Genes GS165527: MP:0005378 growth/size/body region phenotype
Expand Tier I Mouse GO 2134 Genes GS186067: GO:0050877 neurological system process
Expand Tier I Mouse MP 160 Genes GS170701: MP:0004847 abnormal liver weight
Expand Tier II Human 9704 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Mouse MP 121 Genes GS166015: MP:0006036 abnormal mitochondrial physiology
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Mouse 191 Genes GS227188: MSigDB Geneset - GSE11924_TFH_VS_TH1_CD4_TCELL_UP
Expand Tier I Mouse MP 4387 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Mouse MP 427 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human 1261 Genes GS229869: MSigDB Geneset - TATAAA_V$TATA_01
Expand Tier II Human 7556 Genes GS245348: [MeSH] RNA Processing, Post-Transcriptional : D012323
Expand Tier II Human 3864 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier I Mouse GO 2494 Genes GS193018: GO:0003008 system process
Expand Tier I Mouse MP 242 Genes GS166596: MP:0005334 abnormal fat pad morphology
Expand Tier I Human CTD 4077 Genes GS251284: Antirheumatic Agents interacting with Homo sapiens associated genes (MeSH:D018501) in CTD
Expand Tier II Human 29 Genes GS240519: [MeSH] Optic Atrophy : D009896
Expand Tier I Mouse MP 91 Genes GS168434: MP:0002981 increased liver weight
Expand Tier I Human GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Mouse MP 56 Genes GS169160: MP:0004700 abnormal circulating insulin-like growth factor I level
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier II Human 903 Genes GS240994: [MeSH] Alkaloids : D000470
Expand Tier I Mouse MP 3894 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier II Mouse 589 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier III Mouse 8264 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier II Human 255 Genes GS236453: [MeSH] DNA, Circular : D004270
Expand Tier I Mouse GO 11123 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier II Mouse 1020 Genes GS136253: modifier of Dlk1 (mdlk1, Published QTL Chr 7)
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 6547 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 514 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 348 Genes GS228078: MSigDB Geneset - YATGNWAAT_V$OCT_C
Expand Tier I Human 261 Genes GS227884: MSigDB Geneset - V$OCT1_B
Expand Tier II Mouse 581 Genes GS136096: long bones 6 (Lbn6, Published QTL Chr 7)
Expand Tier II Human 10961 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Mouse MP 771 Genes GS164301: MP:0005418 abnormal circulating hormone level
Expand Tier I Human CTD 4077 Genes GS251285: Serotonin Agents interacting with nan associated genes (MeSH:D018490) in CTD
Expand Tier II Mouse 936 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier I Human CTD 1353 Genes GS125069: Sodium Selenite interacting with Homo sapiens associated genes (MeSH:D018038) in CTD
Expand Tier II Mouse 895 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Mouse GO 9716 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 7 Genes GS270222: GWAS Catalog Data for alcohol dependence in 467 European ancestry cases, 407 European ancestry controls
Expand Tier III Human 1759 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating neuronal activity and plasticity in Homo sapiens.
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse MP 2862 Genes GS168995: MP:0009642 abnormal blood homeostasis
Expand Tier I Mouse MP 78 Genes GS168775: MP:0002753 dilated heart left ventricle
Expand Tier I Human 918 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 315 Genes GS231746: PC Geneset - "CCCNNGGGAR_V$OLF1_01" pathway genes
Expand Tier I Mouse 190 Genes GS229173: MSigDB Geneset - GSE17721_CTRL_VS_GARDIQUIMOD_12H_BMDM_DN
Expand Tier I Mouse MP 2319 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier II Human 228 Genes GS239373: [MeSH] DNA, Mitochondrial : D004272
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 256 Genes GS232515: PC Geneset - "V$OCT1_B" pathway genes
Expand Tier I Human GO 14550 Genes GS208012: GO:0044464 cell part
Expand Tier II Mouse 581 Genes GS136238: mandible size 5 (Manz5, Published QTL Chr 7)
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier II Human 8178 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human CTD 10572 Genes GS125506: Valproic Acid interacting with Homo sapiens associated genes (MeSH:D014635) in CTD
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 3057 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier I Human 2195 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Mouse MP 107 Genes GS164826: MP:0010577 abnormal heart right ventricle size
Expand Tier II Human 11279 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Mouse MP 195 Genes GS163855: MP:0000010 abnormal abdominal fat pad morphology
Expand Tier III Mouse 2219 Genes GS216489: Genes that are binding sites of CREB and zif268, transcription factors mediating neuronal activity and plasticity in Mus musculus.
Expand Tier I Human 138 Genes GS229491: MSigDB Geneset - V$AHRARNT_01
Expand Tier II Human 2198 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier I Mouse MP 432 Genes GS168088: MP:0011110 preweaning lethality, incomplete penetrance
Expand Tier II Human 9375 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier II Human 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 412 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse MP 195 Genes GS167836: MP:0001781 abnormal white adipose tissue amount
Expand Tier II Mouse 897 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 87 Genes GS166600: MP:0005330 cardiomyopathy
Expand Tier I Mouse MP 1961 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human 1223 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse MP 2557 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 1731 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 952 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 1143 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse MP 117 Genes GS163841: MP:0008022 dilated heart ventricle
Expand Tier I Human 235 Genes GS232102: PC Geneset - "V$P53_02" pathway genes
Expand Tier I Human 2864 Genes GS229203: MSigDB Geneset - GGGCGGR_V$SP1_Q6
Expand Tier I Mouse MP 175 Genes GS169416: MP:0004937 dilated heart
Expand Tier I Mouse MP 61 Genes GS165032: MP:0009269 decreased fat cell size
Expand Tier I Mouse GO 13185 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse MP 303 Genes GS168021: MP:0000745 tremors
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Mouse MP 236 Genes GS163680: MP:0002970 abnormal white adipose tissue morphology
Expand Tier II Human 1479 Genes GS235868: [MeSH] Carboxylic Acids : D002264
Expand Tier I Human 143 Genes GS232225: PC Geneset - "V$AHRARNT_01" pathway genes
Expand Tier I Mouse MP 2061 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Mouse 192 Genes GS230074: MSigDB Geneset - GSE17721_POLYIC_VS_PAM3CSK4_16H_BMDM_DN
Expand Tier I Mouse MP 74 Genes GS168646: MP:0001429 dehydration
Expand Tier I Mouse MP 19 Genes GS167727: MP:0010398 decreased liver glycogen level
Expand Tier I Human GO 12490 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 1003 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 311 Genes GS229856: MSigDB Geneset - CCCNNGGGAR_V$OLF1_01
Expand Tier I Mouse MP 579 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human 1130 Genes GS228342: MSigDB Geneset - GATTGGY_V$NFY_Q6_01
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Mouse MP 171 Genes GS168682: MP:0000599 enlarged liver
Expand Tier I Human GO 14517 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 7315 Genes GS242876: [MeSH] Proteome : D020543
Expand Tier I Human 11971 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier II Mouse 649 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Human GO 14551 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 11231 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 2876 Genes GS244578: [MeSH] Liver : D008099
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human CTD 1798 Genes GS251957: 3-(2-benzyloxyphenyl)-5-chloromethylisoxazole interacting with nan associated genes (MeSH:C584469) in CTD
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse MP 88 Genes GS164948: MP:0001505 hunched posture
Expand Tier II Human 251 Genes GS236451: [MeSH] Indole Alkaloids : D026121
Expand Tier I Mouse MP 18 Genes GS165239: MP:0010725 thin interventricular septum
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier II Human 14808 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human 238 Genes GS227769: MSigDB Geneset - V$ZF5_B
Expand Tier I Mouse GO 5871 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 2028 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I Human CTD 2300 Genes GS125319: Ethyl Methanesulfonate interacting with Homo sapiens associated genes (MeSH:D005020) in CTD
Expand Tier II Mouse 581 Genes GS136298: maternal performance (Mprf, Published QTL Chr 7)
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier II Mouse 971 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Mouse MP 70 Genes GS167834: MP:0001783 decreased white adipose tissue amount
Expand Tier I Mouse MP 44 Genes GS166238: MP:0002754 dilated heart right ventricle
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier II Human 10244 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Human GO 9519 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 216 Genes GS165811: MP:0009703 decreased birth body size
Expand Tier I Mouse MP 172 Genes GS166048: MP:0009115 abnormal fat cell morphology
Expand Tier I Human 1056 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Human 1675 Genes GS242556: [MeSH] Mitochondria : D008928
Expand Tier I Mouse MP 1022 Genes GS163853: MP:0001547 abnormal lipid level
Expand Tier II Human 5060 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier II Human 238 Genes GS237228: [MeSH] Eye Diseases, Hereditary : D015785
Expand Tier II Human 4490 Genes GS243125: [MeSH] Organic Chemicals : D009930
Expand Tier II Human 2466 Genes GS235341: [MeSH] GTP Phosphohydrolases : D020558
Expand Tier I Mouse MP 834 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier II Human 3527 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 18573 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier II Human 1048 Genes GS240795: [MeSH] Eye Diseases : D005128
Expand Tier I Mouse MP 288 Genes GS163825: MP:0001258 decreased body length
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Mouse GO 1547 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Human GO 5595 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 148 Genes GS167806: MP:0000164 abnormal cartilage development
Expand Tier I Mouse MP 1422 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier II Human 15107 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier I Mouse MP 151 Genes GS167908: MP:0003920 abnormal heart right ventricle morphology
Expand Tier II Human 17884 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Mouse MP 402 Genes GS166404: MP:0002113 abnormal skeleton development
Expand Tier I Mouse MP 1358 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 624 Genes GS170236: MP:0005452 abnormal adipose tissue amount
Expand Tier I Mouse MP 355 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier II Human 4786 Genes GS239448: [MeSH] Heterocyclic Compounds : D006571
Expand Tier II Human 2729 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier II Mouse 969 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Mouse MP 343 Genes GS164555: MP:0005329 abnormal myocardium layer morphology
Expand Tier I Mouse MP 193 Genes GS167439: MP:0000443 abnormal snout morphology
Expand Tier I Mouse MP 224 Genes GS164949: MP:0001504 abnormal posture
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier II Human 17815 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse MP 374 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse MP 2212 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 2614 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human 893 Genes GS228097: MSigDB Geneset - RTAAACA_V$FREAC2_01
Expand Tier II Human 9967 Genes GS234949: [MeSH] Genetic Vectors : D005822
Expand Tier I Mouse MP 3256 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 1234 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse MP 422 Genes GS170776: MP:0000187 abnormal triglyceride level
Expand Tier I Mouse 193 Genes GS227695: MSigDB Geneset - GSE17721_LPS_VS_CPG_16H_BMDM_UP
Expand Tier II Human 922 Genes GS236474: [MeSH] Indoles : D007211
Expand Tier I Human 185 Genes GS230461: MSigDB Geneset - V$FREAC7_01
Expand Tier I Human 179 Genes GS228281: MSigDB Geneset - PRC1_BMI_UP.V1_DN
Expand Tier I Human GO 10580 Genes GS203594: GO:0043226 organelle
Expand Tier I Zebrafish CTD 683 Genes GS261978: sodium arsenate interacting with Danio rerio associated genes (MeSH:C009277) in CTD
Expand Tier II Human 18638 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Mouse MP 82 Genes GS162866: MP:0005241 abnormal retinal ganglion layer morphology