Gene Details



OPA3 and homologs in 6 species are found in 484 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse MP 1246 Genes GS165707: MP:0000428 abnormal craniofacial morphology
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse 200 Genes GS227419: MSigDB Geneset - GSE27786_LSK_VS_LIN_NEG_CELL_UP
Expand Tier II Human 14476 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier I Human 263 Genes GS227508: MSigDB Geneset - V$OCT1_01
Expand Tier II Human 19667 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Mouse MP 1698 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Mouse MP 196 Genes GS168129: MP:0010025 decreased total body fat amount
Expand Tier I Human 187 Genes GS228412: MSigDB Geneset - PRC2_SUZ12_UP.V1_DN
Expand Tier I Mouse 969 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Mouse MP 1039 Genes GS166120: MP:0002106 abnormal muscle physiology
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse MP 241 Genes GS170738: MP:0001056 abnormal cranial nerve morphology
Expand Tier II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier II Mouse 80 Genes GS36017: Striatum Gene expression correlates of Light-Dark Box Total seconds spent in dark compartment in Females & Males BXD
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Mouse 200 Genes GS228984: MSigDB Geneset - GSE7852_TREG_VS_TCONV_FAT_UP
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier II Human 12421 Genes GS239540: [MeSH] Heterochromatin : D006570
Expand Tier II Mouse 86 Genes GS35311: Striatum Gene expression correlates of Acoustic Startle Response Percentage of maximum response at 85 db in Females BXD
Expand Tier I Human 239 Genes GS229232: MSigDB Geneset - V$HFH1_01
Expand Tier I Human 2254 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 224 Genes GS167702: MP:0003141 cardiac fibrosis
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 8563 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Mouse 200 Genes GS229556: MSigDB Geneset - GSE17721_CTRL_VS_GARDIQUIMOD_1H_BMDM_DN
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 1020 Genes GS136319: non-HDL QTL 6 (Nhdlq6, Published QTL Chr 7)
Expand Tier I Mouse MP 3520 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier II Mouse 358 Genes GS35306: Striatum Gene expression correlates of Acoustic Startle Response Percentage of maximum startle response at 80 db in Females & Males BXD
Expand Tier I Mouse MP 388 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse 649 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Mouse MP 71 Genes GS169907: MP:0002090 abnormal vision
Expand Tier I Mouse MP 127 Genes GS169978: MP:0006035 abnormal mitochondrion morphology
Expand Tier I Human 248 Genes GS230204: MSigDB Geneset - V$T3R_Q6
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier III Human 3028 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier II Human 234 Genes GS238669: [MeSH] Amino Acid Metabolism, Inborn Errors : D000592
Expand Tier I Mouse 199 Genes GS230568: MSigDB Geneset - GSE17721_CTRL_VS_POLYIC_4H_BMDM_UP
Expand Tier II Human 9487 Genes GS243358: [MeSH] Protein Transport : D021381
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Human 11446 Genes GS236912: [MeSH] Biological Transport : D001692
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 99 Genes GS235593: [MeSH] Optic Nerve Diseases : D009901
Expand Tier II Human 12580 Genes GS238462: [MeSH] Interspersed Repetitive Sequences : D020071
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier II Human 10604 Genes GS243658: [MeSH] Recombinant Fusion Proteins : D011993
Expand Tier I Mouse 954 Genes GS136745: spermatogenesis defect 3 (Spmd3, Published QTL Chr 7)
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier II Human 41 Genes GS236121: [MeSH] Glutarates : D005977
Expand Tier I Human 265 Genes GS232688: PC Geneset - "V$OCT1_Q5_01" pathway genes
Expand Tier I Mouse MP 1566 Genes GS163852: MP:0001544 abnormal cardiovascular system physiology
Expand Tier I Human 240 Genes GS230791: MSigDB Geneset - V$FOXO1_01
Expand Tier II Mouse 39 Genes GS34260: Cerebellum Gene expression correlates of Suppression of activity in altered context in Females BXD
Expand Tier II Human 30225 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Mouse MP 245 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier I Mouse MP 124 Genes GS163468: MP:0010499 abnormal ventricle myocardium morphology
Expand Tier I Mouse MP 2893 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human 756 Genes GS228578: MSigDB Geneset - MGGAAGTG_V$GABP_B
Expand Tier II Human 1635 Genes GS237329: [MeSH] Acids, Acyclic : D000144
Expand Tier I Human 234 Genes GS232076: PC Geneset - "V$HFH1_01" pathway genes
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Mouse MP 465 Genes GS169228: MP:0001406 abnormal gait
Expand Tier I Human 269 Genes GS228761: MSigDB Geneset - V$OCT1_Q5_01
Expand Tier II Mouse 68 Genes GS34871: Cerebellum Gene expression correlates of Open Field - Percentage center time in Females BXD
Expand Tier II Mouse 262 Genes GS34191: Hippocampus Gene expression correlates of Number of entries into closed arms of plus maze in Males BXD
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Human 196 Genes GS227917: MSigDB Geneset - GSE37416_CTRL_VS_12H_F_TULARENSIS_LVS_NEUTROPHIL_DN
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier II Human 888 Genes GS239294: [MeSH] Heredodegenerative Disorders, Nervous System : D020271
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse MP 187 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier II Human 204 Genes GS239238: [MeSH] Lens Diseases : D007905
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Human 126 Genes GS227776: MSigDB Geneset - V$GRE_C
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier I Human 2005 Genes GS232341: PC Geneset - "TTGTTT_V$FOXO4_01" pathway genes
Expand Tier I Human 231 Genes GS232392: PC Geneset - "V$ZF5_B" pathway genes
Expand Tier I Mouse 969 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 232 Genes GS232673: PC Geneset - "V$FOXO1_01" pathway genes
Expand Tier I Mouse MP 108 Genes GS167462: MP:0002795 dilated cardiomyopathy
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Mouse MP 1015 Genes GS166660: MP:0001731 abnormal postnatal growth
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier I Mouse 827 Genes GS136728: susceptibility to lung cancer 30 (Sluc30, Published QTL Chr 7)
Expand Tier II Human 192 Genes GS235348: [MeSH] Cataract : D002386
Expand Tier II Mouse 262 Genes GS36850: Hippocampus Gene expression correlates of Percentage of entries into closed arms of plus maze in Males BXD
Expand Tier I Mouse MP 316 Genes GS169191: MP:0000281 abnormal interventricular septum morphology
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Mouse MP 799 Genes GS163226: MP:0003312 abnormal locomotor coordination
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Mouse MP 737 Genes GS167833: MP:0001784 abnormal fluid regulation
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier I Mouse MP 519 Genes GS165595: MP:0010545 abnormal heart layer morphology
Expand Tier II Human 9151 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier II Human 18727 Genes GS236759: [MeSH] Intranuclear Space : D042581
Expand Tier I Human 741 Genes GS232218: PC Geneset - "MGGAAGTG_V$GABP_B" pathway genes
Expand Tier II Mouse 44 Genes GS36443: Cerebellum Gene expression correlates of Open Field -Total distance in the perimeter in Females BXD
Expand Tier I Human 2892 Genes GS232583: PC Geneset - "GGGCGGR_V$SP1_Q6" pathway genes
Expand Tier I Mouse MP 2070 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier II Human 160 Genes GS234779: [MeSH] Mitochondrial Diseases : D028361
Expand Tier II Human 173 Genes GS239635: [MeSH] Cranial Nerve Diseases : D003389
Expand Tier II Human 7543 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier II Human 14860 Genes GS240463: [MeSH] Chromatin : D002843
Expand Tier I Mouse MP 323 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I 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 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Mouse 358 Genes GS35286: Striatum Gene expression correlates of Prepulse inhibition at 80db in Females & Males BXD
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier II Human 4450 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I 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 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Mouse MP 18 Genes GS167310: MP:0008513 thin retinal inner plexiform layer
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier II Human 16067 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 260 Genes GS227818: MSigDB Geneset - V$OCT_Q6
Expand Tier I Mouse MP 710 Genes GS168826: MP:0005294 abnormal heart ventricle morphology
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human 189 Genes GS229287: MSigDB Geneset - GSE37416_CTRL_VS_6H_F_TULARENSIS_LVS_NEUTROPHIL_DN
Expand Tier I Mouse MP 3159 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human 2037 Genes GS228205: MSigDB Geneset - TTGTTT_V$FOXO4_01
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Mouse MP 126 Genes GS165074: MP:0010563 increased heart right ventricle size
Expand Tier I Mouse MP 17 Genes GS169901: MP:0008507 thin retinal ganglion layer
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse MP 855 Genes GS169075: MP:0002078 abnormal glucose homeostasis
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Mouse MP 234 Genes GS167797: MP:0008772 increased heart ventricle size
Expand Tier I Mouse MP 974 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier II Human 16797 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Mouse 197 Genes GS229017: MSigDB Geneset - GSE11924_TFH_VS_TH2_CD4_TCELL_UP
Expand Tier II Human 18907 Genes GS242148: [MeSH] Cell Nucleus Structures : D022003
Expand Tier II Human 13815 Genes GS240409: [MeSH] Drosophila Proteins : D029721
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse MP 334 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 1764 Genes GS165386: MP:0001262 decreased body weight
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse 1026 Genes GS128580: BECs at LORR Recovery Chr# 7
Expand Tier I Mouse MP 1119 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier I Mouse MP 1338 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier I Mouse 969 Genes GS135988: Hfe modifier 1 (Hfem1, Published QTL Chr 7)
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier II Human 1039 Genes GS243748: [MeSH] Metabolism, Inborn Errors : D008661
Expand Tier I Mouse MP 2283 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 864 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier II Human 3936 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 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse MP 113 Genes GS166899: MP:0001330 abnormal optic nerve morphology
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse MP 15 Genes GS163514: MP:0006303 abnormal retinal nerve fiber layer morphology
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier II Human 5957 Genes GS240584: [MeSH] Green Fluorescent Proteins : D049452
Expand Tier III Mouse 5790 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Mouse 200 Genes GS227103: MSigDB Geneset - GSE17721_CTRL_VS_LPS_2H_BMDM_DN
Expand Tier II Human 283 Genes GS244540: [MeSH] Lod Score : D008126
Expand Tier I Human 196 Genes GS227316: MSigDB Geneset - GSE24634_IL4_VS_CTRL_TREATED_NAIVE_CD4_TCELL_DAY10_UP
Expand Tier II Mouse 48 Genes GS34247: Hippocampus Gene expression correlates of Activity in altered context during presentation of cue in Females BXD
Expand Tier I Mouse MP 444 Genes GS169957: MP:0001402 hypoactivity
Expand Tier II Human 2379 Genes GS243535: [MeSH] Neurodegenerative Diseases : D019636
Expand Tier I Mouse 199 Genes GS228241: MSigDB Geneset - GSE10239_NAIVE_VS_DAY4.5_EFF_CD8_TCELL_DN
Expand Tier I Human 265 Genes GS230730: MSigDB Geneset - V$OCT_C
Expand Tier I Mouse MP 3424 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse MP 4902 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier II Human 280 Genes GS238561: [MeSH] Dicarboxylic Acids : D003998
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier I Human 187 Genes GS232243: PC Geneset - "V$FREAC7_01" pathway genes
Expand Tier I Mouse 936 Genes GS135417: beta-carboline induced seizures 4 (Bis4, Published QTL Chr 7)
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Human 8327 Genes GS244452: [MeSH] Organ Specificity : D009928
Expand Tier I Human 192 Genes GS228580: MSigDB Geneset - PRC2_EZH2_UP.V1_DN
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 991 Genes GS165869: MP:0002138 abnormal hepatobiliary system morphology
Expand Tier I Mouse MP 375 Genes GS163197: MP:0006113 abnormal heart septum morphology
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human 90 Genes GS229015: MSigDB Geneset - SNACANNNYSYAGA_UNKNOWN
Expand Tier I Mouse MP 436 Genes GS169225: MP:0000358 abnormal cell morphology
Expand Tier I Mouse MP 628 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse MP 687 Genes GS165539: MP:0005375 adipose tissue phenotype
Expand Tier I Mouse DRG 2567 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Mouse MP 73 Genes GS168793: MP:0005439 decreased glycogen level
Expand Tier I Mouse 637 Genes GS136214: lupus BXSB x NZW 6 (Lxw6, Published QTL Chr 7)
Expand Tier I Mouse GO 1603 Genes GS177409: GO:0005739 mitochondrion
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human 248 Genes GS232206: PC Geneset - "V$P53_DECAMER_Q2" pathway genes
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Mouse MP 18 Genes GS166008: MP:0001492 abnormal pilomotor reflex
Expand Tier I Mouse MP 111 Genes GS169367: MP:0005405 axon degeneration
Expand Tier II Mouse 86 Genes GS35291: Striatum Gene expression correlates of Prepulse inhibition at 85db in Females BXD
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 219 Genes GS240862: [MeSH] Staurosporine : D019311
Expand Tier II Human 24024 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Mouse MP 153 Genes GS166015: MP:0006036 abnormal mitochondrial physiology
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Mouse 196 Genes GS227188: MSigDB Geneset - GSE11924_TFH_VS_TH1_CD4_TCELL_UP
Expand Tier I Mouse MP 4624 Genes GS165524: MP:0010769 abnormal survival
Expand Tier I Mouse MP 459 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Human 1279 Genes GS229869: MSigDB Geneset - TATAAA_V$TATA_01
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier II Human 12369 Genes GS245348: [MeSH] RNA Processing, Post-Transcriptional : D012323
Expand Tier II Human 7823 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier I Mouse MP 250 Genes GS166596: MP:0005334 abnormal fat pad morphology
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier II Human 39 Genes GS240519: [MeSH] Optic Atrophy : D009896
Expand Tier I Human GO 1515 Genes GS194138: GO:0005739 mitochondrion
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier II Human 1434 Genes GS240994: [MeSH] Alkaloids : D000470
Expand Tier I Mouse MP 3714 Genes GS165243: MP:0010770 preweaning lethality
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse 589 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier II Human 480 Genes GS236453: [MeSH] DNA, Circular : D004270
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier I Mouse 1020 Genes GS136253: modifier of Dlk1 (mdlk1, Published QTL Chr 7)
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier II Human 22498 Genes GS245206: [MeSH] Cell Nucleus : D002467
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 355 Genes GS228078: MSigDB Geneset - YATGNWAAT_V$OCT_C
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 264 Genes GS227884: MSigDB Geneset - V$OCT1_B
Expand Tier I Mouse 581 Genes GS136096: long bones 6 (Lbn6, Published QTL Chr 7)
Expand Tier II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier II Mouse 45 Genes GS26259: Cerebellum Gene expression correlates of Thermal Nociception Tail Withdrawal Test in Females BXD
Expand Tier I Mouse 936 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
Expand Tier I Human CTD 1192 Genes GS125069: Sodium Selenite interacting genes (MeSH:D018038) in CTD
Expand Tier II Mouse 899 Genes GS84191: alcohol preference 7 QTL (Ap7q, Published QTL, Chr 7)
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier III Human 2161 Genes GS216491: Genes that are binding sites for CREB and zif268,transcription factors mediating nieuronal activity and plasticity, in Homo sapiens.
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Mouse MP 123 Genes GS168775: MP:0002753 dilated heart left ventricle
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 320 Genes GS231746: PC Geneset - "CCCNNGGGAR_V$OLF1_01" pathway genes
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Mouse 199 Genes GS229173: MSigDB Geneset - GSE17721_CTRL_VS_GARDIQUIMOD_12H_BMDM_DN
Expand Tier I Mouse MP 2465 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier II Human 429 Genes GS239373: [MeSH] DNA, Mitochondrial : D004272
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 258 Genes GS232515: PC Geneset - "V$OCT1_B" pathway genes
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse DRG 2567 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Mouse 581 Genes GS136238: mandible size 5 (Manz5, Published QTL Chr 7)
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 73 Genes GS175408: HP:0002071 Abnormality of extrapyramidal motor function
Expand Tier II Human 18456 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human 53 Genes GS175407: HP:0002072 Chorea
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Mouse MP 2111 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 58023 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 5596 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier II Human 12397 Genes GS235736: [MeSH] DNA Transposable Elements : D004251
Expand Tier I Human 2227 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Mouse MP 141 Genes GS164826: MP:0010577 abnormal heart right ventricle size
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Mouse MP 207 Genes GS163855: MP:0000010 abnormal abdominal fat pad morphology
Expand Tier III Mouse 2256 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 140 Genes GS229491: MSigDB Geneset - V$AHRARNT_01
Expand Tier II Human 3263 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier I Mouse MP 157 Genes GS168088: MP:0011110 partial preweaning lethality
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse 897 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 167 Genes GS166600: MP:0005330 cardiomyopathy
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 1743 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 1967 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 181 Genes GS163841: MP:0008022 dilated heart ventricle
Expand Tier I Mouse MP 1548 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human 2919 Genes GS229203: MSigDB Geneset - GGGCGGR_V$SP1_Q6
Expand Tier I Human 243 Genes GS232102: PC Geneset - "V$P53_02" pathway genes
Expand Tier I Mouse MP 300 Genes GS169416: MP:0004937 dilated heart
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse MP 374 Genes GS168021: MP:0000745 tremors
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier II Human 2398 Genes GS235868: [MeSH] Carboxylic Acids : D002264
Expand Tier I Human 144 Genes GS232225: PC Geneset - "V$AHRARNT_01" pathway genes
Expand Tier I Mouse 198 Genes GS230074: MSigDB Geneset - GSE17721_POLYIC_VS_PAM3CSK4_16H_BMDM_DN
Expand Tier I Mouse MP 22 Genes GS167727: MP:0010398 decreased liver glycogen level
Expand Tier I Mouse MP 103 Genes GS168646: MP:0001429 dehydration
Expand Tier I Human 320 Genes GS229856: MSigDB Geneset - CCCNNGGGAR_V$OLF1_01
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 15731 Genes GS236183: [MeSH] Chromosome Structures : D022004
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human 1157 Genes GS228342: MSigDB Geneset - GATTGGY_V$NFY_Q6_01
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier II Mouse 23 Genes GS36142: Striatum Gene expression correlates of Activity during 2ndtone shock pairing in Females BXD
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 15342 Genes GS242876: [MeSH] Proteome : D020543
Expand Tier II Human 12283 Genes GS244576: [MeSH] Genome, Insect : D049750
Expand Tier I Mouse 649 Genes GS135679: Crhr1 transcript abundance QTL 1 (Crhr1taq1, Published QTL Chr 7)
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 5168 Genes GS244578: [MeSH] Liver : D008099
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Mouse MP 128 Genes GS164948: MP:0001505 hunched posture
Expand Tier II Human 344 Genes GS236451: [MeSH] Indole Alkaloids : D026121
Expand Tier I Mouse MP 29 Genes GS165239: MP:0010725 thin interventricular septum
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human 239 Genes GS227769: MSigDB Geneset - V$ZF5_B
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 2105 Genes GS128573: Ethanol Induced Hypothermia Chr# 7
Expand Tier I 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 68 Genes GS35011: Cerebellum Gene expression correlates of Open Field-Total time in perimeter in Females BXD
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Mouse 971 Genes GS136602: sperm beat cross frequency (Sbcf, Published QTL Chr 7)
Expand Tier I Mouse MP 75 Genes GS166238: MP:0002754 dilated heart right ventricle
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse MP 244 Genes GS165811: MP:0009703 decreased birth body size
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Human 4060 Genes GS242556: [MeSH] Mitochondria : D008928
Expand Tier II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier II Human 357 Genes GS237228: [MeSH] Eye Diseases, Hereditary : D015785
Expand Tier II Human 5364 Genes GS235341: [MeSH] GTP Phosphohydrolases : D020558
Expand Tier II Human 9229 Genes GS243125: [MeSH] Organic Chemicals : D009930
Expand Tier I Mouse MP 918 Genes GS165427: MP:0000432 abnormal head morphology
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier II Human 1689 Genes GS240795: [MeSH] Eye Diseases : D005128
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Mouse GO 1550 Genes GS192290: GO:0007600 sensory perception
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 1589 Genes GS165260: MP:0001392 abnormal locomotor behavior
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier I Mouse MP 195 Genes GS167908: MP:0003920 abnormal heart right ventricle morphology
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Mouse MP 1327 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier I Mouse MP 551 Genes GS170236: MP:0005452 abnormal adipose tissue amount
Expand Tier I Mouse MP 542 Genes GS165385: MP:0008946 abnormal neuron number
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier II Human 9423 Genes GS239448: [MeSH] Heterocyclic Compounds : D006571
Expand Tier I Mouse 969 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Mouse MP 510 Genes GS164555: MP:0005329 abnormal myocardium layer morphology
Expand Tier I Mouse MP 208 Genes GS167439: MP:0000443 abnormal snout morphology
Expand Tier I Mouse MP 295 Genes GS164949: MP:0001504 abnormal posture
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse MP 569 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Human 910 Genes GS228097: MSigDB Geneset - RTAAACA_V$FREAC2_01
Expand Tier I Mouse MP 2489 Genes GS165397: MP:0001265 decreased body size
Expand Tier I Mouse MP 3396 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier II Human 13620 Genes GS234949: [MeSH] Genetic Vectors : D005822
Expand Tier II Human 12282 Genes GS234930: [MeSH] Genes, Insect : D017344
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Mouse 199 Genes GS227695: MSigDB Geneset - GSE17721_LPS_VS_CPG_16H_BMDM_UP
Expand Tier I Human 186 Genes GS228281: MSigDB Geneset - PRC1_BMI_UP.V1_DN
Expand Tier I Human 190 Genes GS230461: MSigDB Geneset - V$FREAC7_01
Expand Tier II Human 1483 Genes GS236474: [MeSH] Indoles : D007211
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier II Human 73890 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Mouse MP 116 Genes GS162866: MP:0005241 abnormal retinal ganglion layer morphology
Expand Tier II Human 32928 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier I Human 252 Genes GS227531: MSigDB Geneset - V$P53_02
Expand Tier II Human 5 Genes GS236750: [MeSH] Optic Atrophy, Autosomal Dominant : D029241
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Mouse MP 155 Genes GS167355: MP:0000445 short snout
Expand Tier II Human 13292 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Human 199 Genes GS229166: MSigDB Geneset - V$HFH8_01
Expand Tier I Mouse 2138 Genes GS128593: Average rotarod training latency Chr# 7
Expand Tier I Mouse MP 4019 Genes GS165537: MP:0005376 homeostasis/metabolism phenotype
Expand Tier II Human 6800 Genes GS241330: [MeSH] Heterocyclic Compounds, 2-Ring : D006574
Expand Tier I Mouse 827 Genes GS136263: modifier of mammary tumor growth 3 (Mmtg3, Published QTL Chr 7)
Expand Tier I Mouse MP 553 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier I Human 199 Genes GS229530: MSigDB Geneset - GSE7460_CTRL_VS_FOXP3_OVEREXPR_TCONV_UP
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Mouse MP 854 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 123 Genes GS193540: GO:0007601 visual perception
Expand Tier II Human 30317 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Tier II Human 7917 Genes GS239881: [MeSH] Subcellular Fractions : D013347
Expand Tier I Mouse MP 983 Genes GS164742: MP:0001732 postnatal growth retardation
Expand Tier II Human 56931 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier II Human 30254 Genes GS243763: [MeSH] Intracellular Space : D042541
Expand Tier I Mouse MP 139 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier II Human 8112 Genes GS235286: [MeSH] Cell Death : D016923
Expand Tier I Mouse MP 39 Genes GS169801: MP:0003734 abnormal retinal inner plexiform layer morphology
Expand Tier II Mouse 80 Genes GS36047: Striatum Gene expression correlates of Light- Dark Box Total seconds spent in light compartment in Females & Males BXD
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 898 Genes GS231628: PC Geneset - "RTAAACA_V$FREAC2_01" pathway genes
Expand Tier II Human 2211 Genes GS244905: [MeSH] Mitochondrial Proteins : D024101
Expand Tier II Human 13600 Genes GS235415: [MeSH] Embryo, Mammalian : D004622
Expand Tier II Human 13895 Genes GS244414: [MeSH] Arthropod Proteins : D060829
Expand Tier I Mouse 1019 Genes GS136742: Streptococcus pneumoniae infection resistance 1 (Spir1, Published QTL Chr 7)
Expand Tier I Mouse MP 86 Genes GS170015: MP:0005608 cardiac interstitial fibrosis
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse MP 1065 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier II Human 73218 Genes GS245795: [MeSH] Genes : D005796
Expand Tier II Human 322 Genes GS240378: [MeSH] Carbazoles : D002227
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse MP 728 Genes GS170683: MP:0003743 abnormal facial morphology
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Mouse MP 92 Genes GS170195: MP:0008515 thin retinal outer nuclear layer
Expand Tier I Mouse MP 577 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Mouse 906 Genes GS135938: HDL level 38 (Hdl38, Published QTL Chr 7)
Expand Tier I Mouse MP 623 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse 906 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier I Mouse MP 482 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier II Human 13886 Genes GS245484: [MeSH] Insect Proteins : D019476
Expand Tier I Human 816 Genes GS228126: MSigDB Geneset - chr19q13
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Human 35136 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Mouse MP 87 Genes GS164236: MP:0008056 abnormal retinal ganglion cell morphology
Expand Tier II Human 35 Genes GS243691: [MeSH] Optic Atrophies, Hereditary : D015418
Expand Tier I Mouse MP 37 Genes GS163522: MP:0006309 decreased retinal ganglion cell number
Expand Tier II Human 982 Genes GS241409: [MeSH] Heterocyclic Compounds, 3-Ring : D006575
Expand Tier II Human 12246 Genes GS243456: [MeSH] Euchromatin : D022041
Expand Tier II Human 11662 Genes GS239443: [MeSH] RNA Splicing : D012326
Expand Tier I Human 128 Genes GS232073: PC Geneset - "V$GRE_C" pathway genes
Expand Tier II Human 22746 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier I Human 199 Genes GS232279: PC Geneset - "V$HFH8_01" pathway genes
Expand Tier I