Gene Details



MAN2B1 and homologs in 8 species are found in 939 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 GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier II Human 2152 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier I Mouse MP 193 Genes GS170581: MP:0008987 abnormal liver lobule morphology
Expand Tier I Mouse MP 47 Genes GS168997: MP:0009640 abnormal renal tubule epithelium morphology
Expand Tier III Rat 588 Genes GS224085: Body weight QTL 152 (Bw152 Published QTL Chr 19)
Expand Tier I Mouse 574 Genes GS136137: lithogenic gene 18 (Lith18, Published QTL Chr 8)
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 200 Genes GS228648: MSigDB Geneset - GSE3982_BASOPHIL_VS_CENT_MEMORY_CD4_TCELL_DN
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier II Human 12421 Genes GS239540: [MeSH] Heterochromatin : D006570
Expand Tier II Human 462 Genes GS234684: [MeSH] env Gene Products, Human Immunodeficiency Virus : D054299
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier I Human 200 Genes GS230510: MSigDB Geneset - GSE3982_MAC_VS_BASOPHIL_UP
Expand Tier I Mouse MP 3520 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse 573 Genes GS135547: CD4 T cell subset 3 (Cd4ts3, Published QTL Chr 8)
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Mouse MP 190 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier I Mouse MP 508 Genes GS167046: MP:0003881 abnormal nephron morphology
Expand Tier II Human 11446 Genes GS236912: [MeSH] Biological Transport : D001692
Expand Tier II Human 10106 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier II Human 35 Genes GS237727: [MeSH] AIDS Vaccines : D016915
Expand Tier I Human CTD 377 Genes GS124417: Propylthiouracil interacting genes (MeSH:D011441) in CTD
Expand Tier II Human 143 Genes GS242664: [MeSH] Hexosamines : D006595
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human 60 Genes GS227677: MSigDB Geneset - GNF2_MYD88
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse MP 8 Genes GS166576: MP:0004081 abnormal globus pallidus morphology
Expand Tier II Human 3 Genes GS238685: [MeSH] Mannosidase Deficiency Diseases : D044904
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier II Human 1685 Genes GS241253: [MeSH] Protein Folding : D017510
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier II Human 2639 Genes GS245025: [MeSH] Receptors, Cytokine : D018121
Expand Tier I Mouse 574 Genes GS135948: HDL QTL 16 (Hdlq16, Published QTL Chr 8)
Expand Tier III Rat 592 Genes GS223838: Urinary albumin excretion QTL 39 (Uae39 Published QTL Chr 19)
Expand Tier I Mouse MP 83 Genes GS164483: MP:0005220 abnormal exocrine pancreas morphology
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Mouse 501 Genes GS136657: skeletal muscle weight 16 (Skmw16, Published QTL Chr 8)
Expand Tier II Human 14581 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier III Rat 213 Genes GS224726: Experimental allergic encephalomyelitis QTL 8 (Eae8 Published QTL Chr 19)
Expand Tier I Mouse MP 2220 Genes GS166858: MP:0000685 abnormal immune system morphology
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Mouse MP 28 Genes GS167519: MP:0002802 abnormal discrimination learning
Expand Tier I Human CTD 2014 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human 1 Genes GS171980: HP:0007232 Spinocerebellar tract disease in lower limbs
Expand Tier II Human 432 Genes GS236659: [MeSH] Codon, Terminator : D018388
Expand Tier I Mouse MP 164 Genes GS169585: MP:0001413 abnormal response to new environment
Expand Tier I Human 6 Genes GS172728: HP:0008850 Severe postnatal growth retardation
Expand Tier II Human 94 Genes GS239667: [MeSH] Glucosamine : D005944
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
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 I Mouse MP 243 Genes GS170569: MP:0005404 abnormal axon morphology
Expand Tier I Human 32 Genes GS176916: HP:0004437 Cranial hyperostosis
Expand Tier I Mouse MP 902 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier I Mouse 200 Genes GS228965: MSigDB Geneset - GSE3337_4H_VS_16H_IFNG_IN_CD8POS_DC_DN
Expand Tier II Human 3578 Genes GS243730: [MeSH] Cytoplasmic Vesicles : D022162
Expand Tier I Mouse 419 Genes GS135449: bone length and organs 5 (Bod5, Published QTL Chr 8)
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier II Human 26 Genes GS239748: [MeSH] alpha-Mannosidase : D043323
Expand Tier I Human 199 Genes GS228772: MSigDB Geneset - GSE3982_DC_VS_TH2_UP
Expand Tier I Mouse 18 Genes GS233392: KEGG Geneset - "Other glycan degradation" pathway genes
Expand Tier II Human 174 Genes GS236901: [MeSH] Carbohydrate Metabolism, Inborn Errors : D002239
Expand Tier I Human GO 341 Genes GS207982: GO:0005764 lysosome
Expand Tier I Human 2 Genes GS175466: HP:0007893 Progressive retinal degeneration
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Human GO 404 Genes GS209163: GO:0005773 vacuole
Expand Tier II Human 18727 Genes GS236759: [MeSH] Intranuclear Space : D042581
Expand Tier II Human 3470 Genes GS240837: [MeSH] Polysaccharides : D011134
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Mouse MP 2070 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier II Human 2454 Genes GS245143: [MeSH] Monosaccharides : D009005
Expand Tier I Human 197 Genes GS229960: MSigDB Geneset - GSE29618_BCELL_VS_PDC_DAY7_FLU_VACCINE_DN
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Mouse MP 323 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 175 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier I Human 88 Genes GS173557: HP:0005372 Abnormality of B cell physiology
Expand Tier I Human 193 Genes GS228060: MSigDB Geneset - GSE12366_GC_VS_MEMORY_BCELL_DN
Expand Tier I Mouse MP 533 Genes GS163994: MP:0008248 abnormal mononuclear phagocyte morphology
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
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 Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 9 Genes GS174506: HP:0100712 Abnormality of the lumbar spine
Expand Tier II Human 1998 Genes GS244732: [MeSH] Protein Precursors : D011498
Expand Tier I Human 25 Genes GS175546: HP:0010885 Aseptic necrosis
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier II Human 908 Genes GS242101: [MeSH] Sexually Transmitted Diseases : D012749
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier II Human 6955 Genes GS245398: [MeSH] Protein Isoforms : D020033
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 201 Genes GS245479: [MeSH] Plant Lectins : D037121
Expand Tier II Human 780 Genes GS240871: [MeSH] Membrane Fusion Proteins : D050576
Expand Tier II Mouse 409 Genes GS84205: chronic alcohol withdrawal severity (Published QTL, Chr 8)
Expand Tier I Mouse MP 13 Genes GS168413: MP:0004292 abnormal spiral ligament fibrocyte morphology
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier II Human 6568 Genes GS235980: [MeSH] Mechanical Phenomena : D055595
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Mouse 718 Genes GS128597: Ethanol Induced Ataxia Chr#8
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse GO 560 Genes GS189224: GO:0007610 behavior
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier III Mouse 7843 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier II Human 4568 Genes GS239065: [MeSH] Urinary Tract : D014551
Expand Tier I Mouse 542 Genes GS135540: cerebellum weight 2 (Cbm2, Published QTL Chr 8)
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
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 974 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier II Human 496 Genes GS235219: [MeSH] Antigens, CD4 : D015704
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier II Human 9312 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier I Human 200 Genes GS227543: MSigDB Geneset - GSE22886_NAIVE_BCELL_VS_DC_DN
Expand Tier I Human 192 Genes GS228891: MSigDB Geneset - GSE12366_GC_VS_NAIVE_BCELL_DN
Expand Tier III Rat 526 Genes GS224976: Serum corticosterone level QTL 11 (Scort11 Published QTL Chr 19)
Expand Tier I Human 12 Genes GS170954: HP:0000885 Broad ribs
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier II Human 1261 Genes GS243450: [MeSH] Virus Physiological Phenomena : D018406
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Mouse MP 10 Genes GS165603: MP:0008265 abnormal hippocampus CA2 region morphology
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier III Rat 788 Genes GS223499: Urinary albumin excretion QTL 12 (Uae12 Published QTL Chr 19)
Expand Tier I Human 22 Genes GS173334: HP:0000687 Widely spaced teeth
Expand Tier I Mouse 200 Genes GS227423: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN2_THYMOCYTE_FETAL_UP
Expand Tier I Human 70 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier III Rat 286 Genes GS224968: Serum cholesterol level QTL 12 (Scl12 Published QTL Chr 19)
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 157 Genes GS241239: [MeSH] Viral Fusion Proteins : D014760
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 4298 Genes GS241873: [MeSH] Glycoconjugates : D006001
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse MP 31 Genes GS164960: MP:0002856 abnormal vestibular ganglion morphology
Expand Tier I Human 87 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human 104 Genes GS173512: HP:0000306 Abnormality of the chin
Expand Tier I Human CTD 238 Genes GS121381: fumonisin B1 interacting genes (MeSH:C056933) in CTD
Expand Tier I Mouse 200 Genes GS227994: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN3_THYMOCYTE_ADULT_UP
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse 586 Genes GS135972: wound healing/regeneration 1 (Heal1, Published QTL Chr 8)
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 16 Genes GS173187: HP:0007772 Impaired smooth pursuit
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier II Human 13521 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Mouse 198 Genes GS229957: MSigDB Geneset - GSE13306_RA_VS_UNTREATED_TCONV_UP
Expand Tier I Mouse MP 724 Genes GS168155: MP:0005502 abnormal renal/urinary system physiology
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse MP 84 Genes GS166540: MP:0009820 abnormal liver vasculature morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 200 Genes GS228269: MSigDB Geneset - GSE24634_TEFF_VS_TCONV_DAY10_IN_CULTURE_DN
Expand Tier I Human 5 Genes GS176229: HP:0004570 Increased vertebral height
Expand Tier I Mouse MP 12 Genes GS168016: MP:0003686 abnormal eye muscle morphology
Expand Tier I Human 138 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Mouse MP 784 Genes GS169303: MP:0008250 abnormal myeloid leukocyte morphology
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 18 Genes GS173403: HP:0002684 Thickened calvaria
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Human 1770 Genes GS246716: Muscle function and aging - female Set 2
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 84 Genes GS176462: HP:0100240 Synostosis of joints
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier II Human 482 Genes GS240405: [MeSH] Gene Products, env : D015686
Expand Tier II Human 212 Genes GS234380: [MeSH] Vaccines : D014612
Expand Tier I Human 20 Genes GS175409: HP:0002070 Limb ataxia
Expand Tier I Mouse 849 Genes GS128577: Ethanol induced LORR Chr# 8
Expand Tier I Mouse MP 230 Genes GS163662: MP:0005277 abnormal brainstem morphology
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier I Mouse MP 53 Genes GS167466: MP:0002799 abnormal passive avoidance behavior
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier II Human 7823 Genes GS235095: [MeSH] Digestive System : D004064
Expand Tier II Human 771 Genes GS239200: [MeSH] Receptors, HIV : D015728
Expand Tier I Human 16 Genes GS174507: HP:0100711 Abnormality of the thoracic spine
Expand Tier II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Mouse MP 472 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 153 Genes GS240352: [MeSH] Lysosomal Storage Diseases : D016464
Expand Tier I Human 86 Genes GS176008: HP:0010701 Abnormal immunoglobulin level
Expand Tier I Mouse GO 2303 Genes GS177598: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier II Human 1140 Genes GS240484: [MeSH] Antigens, Differentiation, T-Lymphocyte : D000945
Expand Tier II Mouse 118 Genes GS35078: Striatum Gene expression correlates of Difference in time on rotarod between training and saline in Females & Males BXD
Expand Tier I Human 61 Genes GS174926: HP:0000768 Pectus carinatum
Expand Tier I Mouse MP 1634 Genes GS166250: MP:0008247 abnormal mononuclear cell morphology
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier II Human 615 Genes GS234720: [MeSH] Glycopeptides : D006020
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 II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Human 496 Genes GS239416: [MeSH] Receptors, Interleukin-16 : D053721
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Mouse MP 151 Genes GS162983: MP:0002356 abnormal spleen red pulp morphology
Expand Tier I Human GO 18 Genes GS209597: GO:0005537 mannose binding
Expand Tier II Human 38 Genes GS234644: [MeSH] Swainsonine : D017026
Expand Tier II Human 1210 Genes GS235850: [MeSH] Virus Physiological Processes : D055681
Expand Tier I Mouse 168 Genes GS229064: MSigDB Geneset - GCNP_SHH_UP_EARLY.V1_DN
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Mouse MP 1811 Genes GS168422: MP:0000716 abnormal immune system cell morphology
Expand Tier I Mouse 519 Genes GS135589: P. chabaudi malaria resistance QTL 2 (Char2, Published QTL Chr 8)
Expand Tier I Human GO 72 Genes GS198454: GO:0048029 monosaccharide binding
Expand Tier I Human GO 333 Genes GS204027: GO:0044708 single-organism behavior
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier II Human 34 Genes GS238375: [MeSH] Imino Pyranoses : D050112
Expand Tier II Human 9473 Genes GS241940: [MeSH] Urogenital System : D014566
Expand Tier I Mouse 417 Genes GS136032: induction of brown adipocytes 3 (Iba3, Published QTL Chr 8)
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier II Human 2327 Genes GS241735: [MeSH] Molecular Weight : D008970
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 141 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 2551 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Mouse MP 1548 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human CTD 916 Genes GS121965: Amiodarone interacting genes (MeSH:D000638) in CTD
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Mouse MP 1674 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Human 123 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 15731 Genes GS236183: [MeSH] Chromosome Structures : D022004
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Mouse MP 267 Genes GS167289: MP:0001463 abnormal spatial learning
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Human 199 Genes GS229046: MSigDB Geneset - GSE22886_NAIVE_CD8_TCELL_VS_DC_DN
Expand Tier II Human 290 Genes GS237860: [MeSH] Amino Sugars : D000606
Expand Tier I Mouse MP 64 Genes GS169566: MP:0001092 abnormal trigeminal ganglion morphology
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 129 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Mouse GO 13 Genes GS185006: GO:0015923 mannosidase activity
Expand Tier II Human 478 Genes GS236988: [MeSH] HIV Antigens : D015488
Expand Tier I Mouse MP 60 Genes GS170285: MP:0004967 abnormal kidney epithelium morphology
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse MP 183 Genes GS167518: MP:0001312 abnormal cornea morphology
Expand Tier I Mouse MP 632 Genes GS169386: MP:0002063 abnormal learning/memory/conditioning
Expand Tier II Human 867 Genes GS245305: [MeSH] Sexually Transmitted Diseases, Viral : D015229
Expand Tier I Human GO 13 Genes GS201821: GO:0015923 mannosidase activity
Expand Tier II Human 23476 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier II Human 5168 Genes GS244578: [MeSH] Liver : D008099
Expand Tier II Human 5087 Genes GS234776: [MeSH] Endocrine System : D004703
Expand Tier I Human 13 Genes GS172942: HP:0002942 Thoracic kyphosis
Expand Tier I Human GO 341 Genes GS197314: GO:0000323 lytic vacuole
Expand Tier I Human 191 Genes GS228982: MSigDB Geneset - GSE25087_TREG_VS_TCONV_FETUS_DN
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier II Human 2960 Genes GS236288: [MeSH] Amino Acids, Neutral : D021542
Expand Tier I Human 63 Genes GS172617: HP:0004313 Hypogammaglobulinemia
Expand Tier II Human 955 Genes GS234765: [MeSH] Receptors, Virus : D011991
Expand Tier I Mouse MP 2204 Genes GS165615: MP:0002123 abnormal hematopoiesis
Expand Tier II Human 15607 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier II Human 499 Genes GS235763: [MeSH] Chromosomes, Human, Pair 19 : D002888
Expand Tier I Mouse 444 Genes GS136390: autoimmune orchitis resistance 6 (Orch6, Published QTL Chr 8)
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Mouse GO 219 Genes GS179910: GO:0030246 carbohydrate binding
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier II Human 2299 Genes GS239523: [MeSH] Serine Endopeptidases : D012697
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier II Human 1452 Genes GS241704: [MeSH] Lectins : D037102
Expand Tier I Monkey 16 Genes GS232794: KEGG Geneset - "Other glycan degradation" pathway genes
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier III Rat 515 Genes GS224232: Collagen induced arthritis QTL 14 (Cia14 Published QTL Chr 19)
Expand Tier II Human 7492 Genes GS234348: [MeSH] Inorganic Chemicals : D007287
Expand Tier I Human 46 Genes GS170961: HP:0000158 Macroglossia
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Human 5015 Genes GS240747: [MeSH] Endocrine Glands : D004702
Expand Tier I Mouse MP 3168 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier II Human 3642 Genes GS239875: [MeSH] Immune System Diseases : D007154
Expand Tier II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier I Mouse GO 19 Genes GS192655: GO:0005537 mannose binding
Expand Tier I Mouse MP 1235 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier II Human 9229 Genes GS243125: [MeSH] Organic Chemicals : D009930
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 414 Genes GS135268: alopecia areata 3 (Alaa3, Published QTL Chr 8)
Expand Tier I Mouse MP 832 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 80 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier II Human 3013 Genes GS240174: [MeSH] Isoenzymes : D007527
Expand Tier I Human 94 Genes GS173327: HP:0005368 Abnormality of humoral immunity
Expand Tier III Rat 759 Genes GS224004: Urinary albumin excretion QTL 29 (Uae29 Published QTL Chr 19)
Expand Tier III Rat 526 Genes GS224326: Urine mineral level QTL 5 (Uminl5 Published QTL Chr 19)
Expand Tier I Human CTD 671 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 20 Genes GS171661: HP:0000617 Abnormality of ocular smooth pursuit
Expand Tier I Mouse DRG 938 Genes provisional GS86984: Table S2: The data provided represent genes showing differential expression using ANOVA. A. Genes showing main effect of strain. [DRG]
Expand Tier II Human 8626 Genes GS243166: [MeSH] Pharmacologic Actions : D020228
Expand Tier I Mouse MP 656 Genes GS165538: MP:0005377 hearing/vestibular/ear phenotype
Expand Tier II Human 5263 Genes GS236400: [MeSH] Receptors, Immunologic : D011971
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human 56 Genes GS173337: HP:0000689 Dental malocclusion
Expand Mouse 1119 Genes GS216490: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Tier I Mouse MP 16 Genes GS168111: MP:0008114 abnormal Kupffer cell morphology
Expand Tier I Mouse MP 611 Genes GS163101: MP:0008540 abnormal cerebrum morphology
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier II Human 35 Genes GS240905: [MeSH] Imino Sugars : D050111
Expand Tier I Mouse MP 1798 Genes GS164022: MP:0008246 abnormal leukocyte morphology
Expand Tier I Human 41 Genes GS175197: HP:0002066 Gait ataxia
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse MP 553 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier II Human 30317 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Tier II Human 69 Genes GS234347: [MeSH] Neuraminidase : D009439
Expand Tier I Mouse GO 1341 Genes GS186836: GO:0008270 zinc ion binding
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier I Mouse MP 365 Genes GS164530: MP:0000801 abnormal temporal lobe morphology
Expand Tier I Human 1287 Genes GS227864: MSigDB Geneset - GGGTGGRR_V$PAX4_03
Expand Tier I Mouse MP 524 Genes GS169658: MP:0002572 abnormal emotion/affect behavior
Expand Tier II Human 150 Genes GS244694: [MeSH] HIV Envelope Protein gp41 : D015700
Expand Tier II Human 13895 Genes GS244414: [MeSH] Arthropod Proteins : D060829
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Human 108 Genes GS239037: [MeSH] Mannose : D008358
Expand Tier I Mouse GO 440 Genes GS188916: GO:0044723 single-organism carbohydrate metabolic process
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse 519 Genes GS136533: preaxial shift (Prxsh, Published QTL Chr 8)
Expand Tier I Human 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human GO 168 Genes GS209865: GO:0050890 cognition
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human 6 Genes GS175783: HP:0002503 Spinocerebellar tract degeneration
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Mouse MP 623 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier II Human 1301 Genes GS235959: [MeSH] Complex Mixtures : D045424
Expand Tier II Human 13886 Genes GS245484: [MeSH] Insect Proteins : D019476
Expand Tier I Human GO 12 Genes GS208375: GO:0004559 alpha-mannosidase activity
Expand Tier I Mouse 574 Genes GS136313: non-HDL QTL 1 (Nhdlq1, Published QTL Chr 8)
Expand Tier I Human GO 507 Genes GS206091: GO:0007610 behavior
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse DRG 1196 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Mouse 586 Genes GS135989: Hfe modifier 2 (Hfem2, Published QTL Chr 8)
Expand Tier II Human 12246 Genes GS243456: [MeSH] Euchromatin : D022041
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 57 Genes GS174337: HP:0002718 Recurrent bacterial infections
Expand Tier I Mouse MP 1415 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Mouse 573 Genes GS136068: immune response to AAV2 QTL 2 (Imraq2, Published QTL Chr 8)
Expand Tier I Mouse 419 Genes GS135913: glomerulsclerosis index 1 (Gsi1, Published QTL Chr 8)
Expand Tier I Human 108 Genes GS172118: HP:0004332 Abnormality of lymphocytes
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Mouse MP 837 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse MP 569 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Human 226 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier II Human 9287 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier I Human 134 Genes GS171627: HP:0000470 Short neck
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier II Human 14234 Genes GS242721: [MeSH] Physical Phenomena : D055585
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 3424 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 64 Genes GS176627: HP:0000457 Flat nose
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Human 8327 Genes GS244452: [MeSH] Organ Specificity : D009928
Expand Mouse 1119 Genes GS216461: Differential expression of the liver after chronic ethanol exposure in mice.
Expand Tier I Mouse MP 66 Genes GS165135: MP:0003008 enhanced long term potentiation
Expand Tier I Human 173 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier III Rat 591 Genes GS223227: Alcohol response QTL 21 (Alcrsp21 Published QTL Chr 19)
Expand Tier I Mouse MP 436 Genes GS169225: MP:0000358 abnormal cell morphology
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier II Human 4428 Genes GS241824: [MeSH] Antigens, Differentiation : D000943
Expand Tier I Mouse MP 247 Genes GS163316: MP:0000035 abnormal membranous labyrinth morphology
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 57 Genes GS167534: MP:0009145 abnormal pancreatic acinus morphology
Expand Tier III Mouse 213 Genes GS824: UCSD_CEREBELLUM_Int_Age_Geno
Expand Tier I Human 199 Genes GS227501: MSigDB Geneset - GSE24634_TEFF_VS_TCONV_DAY3_IN_CULTURE_DN
Expand Tier I Mouse 573 Genes GS136920: vertebral morphology and mechanical traits 8 (Vmmt8, Published QTL Chr 8)
Expand Tier II Human 822 Genes GS235254: [MeSH] Viral Structural Proteins : D015678
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier II Human 15964 Genes GS237339: [MeSH] Regulatory Sequences, Nucleic Acid : D012045
Expand Tier II Human 4481 Genes GS243574: [MeSH] Kidney : D007668
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier II Human 1415 Genes GS245443: [MeSH] Retroviridae Proteins : D012191
Expand Tier I Human 199 Genes GS230764: MSigDB Geneset - GSE13484_UNSTIM_VS_3H_YF17D_VACCINE_STIM_PBMC_UP
Expand Tier I Mouse 574 Genes GS136369: obesity QTL 16 (Obq16, Published QTL Chr 8)
Expand Tier II Human 1906 Genes GS240149: [MeSH] Microbiological Phenomena : D008827
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier II Human 13694 Genes GS241851: [MeSH] Receptors, Cell Surface : D011956
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Mouse MP 357 Genes GS167748: MP:0000788 abnormal cerebral cortex morphology
Expand Tier III Rat 236 Genes GS224251: Non-insulin dependent diabetes mellitus QTL 38 (Niddm38 Published QTL Chr 19)
Expand Tier II Mouse 42 Genes GS35264: Whole Brain Gene expression correlates of Maximum startle response to 80 db in Females BXD
Expand Tier II Human 18456 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier II Human 8647 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier I Human 1498 Genes GS230639: MSigDB Geneset - CAGCTG_V$AP4_Q5
Expand Tier I Human GO 786 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Mouse MP 165 Genes GS164751: MP:0000607 abnormal hepatocyte morphology
Expand Tier I Human CTD 573 Genes GS124594: 3-(4'-hydroxy-3'-adamantylbiphenyl-4-yl)acrylic acid interacting genes (MeSH:C472791) in CTD
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier II Human 2208 Genes GS238152: [MeSH] Protein Interaction Maps : D060066
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier III Mouse 2612 Genes GS866: Linear decrease in expression in both Pax6 (Sey) mutants and controls.
Expand Tier I Mouse MP 1015 Genes GS166825: MP:0000462 abnormal digestive system morphology
Expand Tier II Human 14476 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier I Mouse MP 661 Genes GS169304: MP:0008251 abnormal phagocyte morphology
Expand Tier II Human 19440 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier I Mouse MP 29 Genes GS167249: MP:0008267 abnormal hippocampus CA3 region morphology
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 279 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier I Human 33 Genes GS172194: HP:0002970 Genu varum
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier II Human 6632 Genes GS241841: [MeSH] Genitalia : D005835
Expand Tier I Mouse MP 68 Genes GS164269: MP:0000815 abnormal Ammon gyrus morphology
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 198 Genes GS227116: MSigDB Geneset - GSE3982_DC_VS_EFF_MEMORY_CD4_TCELL_UP
Expand Tier II Human 1415 Genes GS234378: [MeSH] Microbiological Processes : D055679
Expand Tier I Mouse GO 10 Genes GS181760: GO:0006013 mannose metabolic process
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse 200 Genes GS228728: MSigDB Geneset - GSE24142_EARLY_THYMIC_PROGENITOR_VS_DN2_THYMOCYTE_UP
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 73 Genes GS181665: GO:0048029 monosaccharide binding
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier III Rat 404 Genes GS224167: Cardiac mass QTL 9 (Cm9 Published QTL Chr 19)
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier II Human 181 Genes GS234325: [MeSH] Carbohydrate Sequence : D002240
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Mouse MP 388 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Human 200 Genes GS228497: MSigDB Geneset - GSE22886_NAIVE_TCELL_VS_DC_DN
Expand Tier I Monkey 117 Genes GS232823: KEGG Geneset - "Lysosome" pathway genes
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Mouse GO 224 Genes GS191043: GO:0005996 monosaccharide metabolic process
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Mouse GO 2223 Genes GS179830: GO:0006464 cellular protein modification process
Expand Tier I Mouse MP 267 Genes GS167356: MP:0002207 abnormal long term potentiation
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 116 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Mouse MP 47 Genes GS165610: MP:0008989 abnormal liver sinusoid morphology
Expand Tier II Human 12580 Genes GS238462: [MeSH] Interspersed Repetitive Sequences : D020071