Gene Details



MFSD8 and homologs in 8 species are found in 368 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 II Human 6197 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier I Mouse MP 661 Genes GS169304: MP:0008251 abnormal phagocyte morphology
Expand Tier I Mouse MP 1190 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Human CTD 6060 Genes GS122891: Copper Sulfate interacting with Homo sapiens associated genes (MeSH:D019327) in CTD
Expand Tier I Human 193 Genes GS229520: MSigDB Geneset - GCM_RAN
Expand Tier I Human 122 Genes GS233764: KEGG Geneset - "Lysosome" pathway genes
Expand Tier II Mouse 200 Genes GS135753: experimental allergic encephalomyelitis susceptibility 20 (Eae20, Published QTL Chr 3)
Expand Tier I Mouse GO 13255 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier II Mouse 178 Genes GS135998: HIV-associated nephropathy 1 (Hivan1, Published QTL Chr 3)
Expand Tier I Mouse GO 8629 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 108 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Mouse GO 8649 Genes GS186743: GO:0043227 membrane-bounded organelle
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 I Monkey 120 Genes GS232823: KEGG Geneset - "Lysosome" pathway genes
Expand Tier I Mouse MP 151 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
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 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Mouse MP 159 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
Expand Tier I Mouse GO 22753 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Mouse 350 Genes GS135597: cholesterol and HDL QTL 2 (Chldq2, Published QTL Chr 3)
Expand Tier II Human 2992 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse 194 Genes GS229937: MSigDB Geneset - GSE17721_CTRL_VS_LPS_24H_BMDM_DN
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human 11 Genes GS172189: HP:0002180 Neurodegeneration
Expand Tier II Human 803 Genes GS238558: [MeSH] Tandem Repeat Sequences : D020080
Expand Tier I Human 1207 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse MP 68 Genes GS169235: MP:0000136 abnormal microglial cell morphology
Expand Tier I Mouse GO 5732 Genes GS190713: GO:0016021 integral to membrane
Expand Tier II Human 21 Genes GS243298: [MeSH] Neuronal Ceroid-Lipofuscinoses : D009472
Expand Tier I Mouse 123 Genes GS233518: KEGG Geneset - "Lysosome" pathway genes
Expand Tier I Mouse MP 637 Genes GS168389: MP:0001186 pigmentation phenotype
Expand Tier I Mouse MP 2131 Genes GS166858: MP:0000685 abnormal immune system morphology
Expand Tier I Mouse MP 2295 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier III Fly 2475 Genes GS213271: Head and thorax heatmapping of Canton-S fruit flies with dietary restrictions
Expand Tier II Human 4996 Genes GS236915: [MeSH] Genome, Human : D015894
Expand Tier I Mouse 189 Genes GS227523: MSigDB Geneset - GSE17721_POLYIC_VS_CPG_1H_BMDM_UP
Expand Tier I Mouse GO 13184 Genes GS191106: GO:0044464 cell part
Expand Tier II Human 1770 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
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 Mouse 191 Genes GS229591: MSigDB Geneset - GSE27786_NKCELL_VS_ERYTHROBLAST_UP
Expand Tier I Mouse MP 738 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Human 1056 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human CTD 3339 Genes GS126466: Quercetin interacting with Homo sapiens associated genes (MeSH:D011794) in CTD
Expand Tier I Mouse MP 2983 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier II Human 1650 Genes GS243730: [MeSH] Cytoplasmic Vesicles : D022162
Expand Tier I Mouse GO 3999 Genes GS183543: GO:0051179 localization
Expand Tier I Human CTD 3845 Genes GS126898: Methyl Methanesulfonate interacting with Homo sapiens associated genes (MeSH:D008741) in CTD
Expand Tier I Mouse MP 999 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Mouse MP 74 Genes GS166313: MP:0008450 retinal photoreceptor degeneration
Expand Tier I Mouse MP 103 Genes GS170334: MP:0003345 decreased rib number
Expand Tier II Mouse 244 Genes GS136077: inspiratory timing at baseline QTL 1 (Itbq1, Published QTL Chr 3)
Expand Tier II Human 3527 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier III Fly 2478 Genes GS213272: Head and thorax heatmapping of reservatrol treated Canton-S fruit flies
Expand Tier I Human GO 3311 Genes GS209452: GO:0006810 transport
Expand Tier II Human 18573 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier II Mouse 242 Genes GS135413: bar holding four paws (Bh4p, Published QTL Chr 3)
Expand Tier II Mouse 178 Genes GS136829: thymocyte proliferative response 3 (Thypr3, Published QTL Chr 3)
Expand Tier I Human GO 342 Genes GS207982: GO:0005764 lysosome
Expand Tier II Mouse 150 Genes GS26244: Cerebellum Gene expression correlates of Mechanical Nociception - Tail Clip Test in Females BXD
Expand Tier II Human 15107 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier I Mouse MP 349 Genes GS165595: MP:0010545 abnormal heart layer morphology
Expand Tier I Human GO 405 Genes GS209163: GO:0005773 vacuole
Expand Tier II Human 17884 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier II Mouse 244 Genes GS84148: ethanol withdrawal (Published QTL, Chr 3)
Expand Tier II Mouse 230 Genes GS136047: insulin dependent diabetes susceptibility 3 (Idd3, Published QTL Chr 3)
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse MP 1358 Genes GS163971: MP:0002092 abnormal eye morphology
Expand Tier II Human 2729 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human GO 3365 Genes GS194459: GO:0051234 establishment of localization
Expand Tier II Mouse 244 Genes GS84147: ethanol conditioned taste aversion (Published QTL, Chr 3)
Expand Tier I Mouse MP 343 Genes GS164555: MP:0005329 abnormal myocardium layer morphology
Expand Tier I Mouse MP 303 Genes GS166591: MP:0004087 abnormal muscle fiber morphology
Expand Tier I Human 62 Genes GS228001: MSigDB Geneset - GCM_ERBB2IP
Expand Tier I Mouse MP 273 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Mouse GO 324 Genes GS192230: GO:0005773 vacuole
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 17815 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse CTD 6842 Genes GS257237: Benzo(a)pyrene interacting with Mus musculus associated genes (MeSH:D001564) in CTD
Expand Tier I Mouse MP 374 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier I Mouse CTD 6019 Genes GS257379: Acetaminophen interacting with Mus musculus associated genes (MeSH:D000082) in CTD
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Mouse MP 507 Genes GS163994: MP:0008248 abnormal mononuclear phagocyte morphology
Expand Tier I Mouse 188 Genes GS227336: MSigDB Geneset - GSE13306_TREG_VS_TCONV_DN
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Mouse MP 3256 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier II Human 3924 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse MP 330 Genes GS167805: MP:0000150 abnormal rib morphology
Expand Tier II Human 158 Genes GS238967: [MeSH] Lipid Metabolism, Inborn Errors : D008052
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Mouse GO 886 Genes GS192671: GO:0055085 transmembrane transport
Expand Tier I Human 196 Genes GS229916: MSigDB Geneset - GSE7460_TCONV_VS_TREG_THYMUS_UP
Expand Tier II Human 2605 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I Mouse 189 Genes GS230371: MSigDB Geneset - GSE7852_TREG_VS_TCONV_THYMUS_DN
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 CTD 2539 Genes GS255987: N-Methyl-3,4-methylenedioxyamphetamine interacting with Mus musculus associated genes (MeSH:D018817) in CTD
Expand Tier I Human GO 10580 Genes GS203594: GO:0043226 organelle
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier II Human 18638 Genes GS239190: [MeSH] Genome : D016678
Expand Tier II Mouse 224 Genes GS135545: CD4 T cell subset 1 (Cd4ts1, Published QTL Chr 3)
Expand Tier II Mouse 175 Genes GS135878: femur geometry 2 (Fmgty2, Published QTL Chr 3)
Expand Tier I Mouse 190 Genes GS230688: MSigDB Geneset - GSE17721_LPS_VS_POLYIC_24H_BMDM_UP
Expand Tier II Mouse 210 Genes GS136404: organ weight QTL 4 (Orgwq4, Published QTL Chr 3)
Expand Tier II Human 6703 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Zebrafish CTD 2626 Genes GS261992: benzo(b)fluoranthene interacting with Danio rerio associated genes (MeSH:C006703) in CTD
Expand Tier I Mouse MP 1251 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Mouse 194 Genes GS228899: MSigDB Geneset - GSE15324_ELF4_KO_VS_WT_NAIVE_CD8_TCELL_UP
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Mouse MP 1674 Genes GS164022: MP:0008246 abnormal leukocyte morphology
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 7665 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Mouse 191 Genes GS230303: MSigDB Geneset - GSE14308_NAIVE_CD4_TCELL_VS_NATURAL_TREG_UP
Expand Tier II Human 637 Genes GS236202: [MeSH] Microsatellite Repeats : D018895
Expand Tier II Human 2529 Genes GS241608: [MeSH] Haplotypes : D006239
Expand Tier I Human 37 Genes GS270147: GWAS Catalog Data for insulin sensitivity measurement, glucose homeostasis measurement in up to 4,176 Mexican American individuals
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Mouse MP 629 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Mouse GO 9739 Genes GS186744: GO:0043226 organelle
Expand Tier II Mouse 148 Genes GS129078: autoimmune ovarian dysgenesis 2 (Aod2 Published QTL Chr 3)
Expand Tier I Human 40 Genes GS227546: MSigDB Geneset - chr4q28
Expand Tier I Mouse MP 3256 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Mouse MP 941 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Mouse GO 11363 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9530 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse GO 274 Genes GS191074: GO:0005764 lysosome
Expand Tier II Mouse 233 Genes GS84144: METH responses for home cage activity (Published QTL, Chr 3)
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier III Mouse 5611 Genes GS213074: Genes with suggestive difference in (C57BL/6 x PWD)F1 vs [(PWD x C57BL/6)F1 + C57BL/6 + PWD] comparison
Expand Tier I Human 164 Genes GS229070: MSigDB Geneset - GCM_GSPT1
Expand Tier II Human 17816 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier III Mouse 7750 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampus
Expand Tier I Mouse GO 5857 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier II Human 7732 Genes GS243763: [MeSH] Intracellular Space : D042541
Expand Tier I Human GO 6258 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Mouse MP 786 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human 1489 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 122 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human GO 9089 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Mouse MP 759 Genes GS166585: MP:0001510 abnormal coat appearance
Expand Tier I Mouse GO 22332 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5251 Genes GS207615: GO:0016021 integral to membrane
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Human GO 10565 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier III Mouse 120 Genes GS26275: Hippocampus Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold [Pain] in Males BXD
Expand Tier II Human 18556 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Human 47 Genes GS171072: HP:0000572 Visual loss
Expand Tier I Mouse MP 834 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier II Human 7025 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Mouse GO 6471 Genes GS184448: GO:0044425 membrane part
Expand Tier II Human 7440 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 80 Genes GS241770: [MeSH] Lipidoses : D008064
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human GO 5911 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse MP 394 Genes GS165985: MP:0000965 abnormal sensory neuron morphology
Expand Tier I Zebrafish CTD 1799 Genes GS261758: Atrazine interacting with Danio rerio associated genes (MeSH:D001280) in CTD
Expand Tier I Mouse MP 697 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Human 184 Genes GS230092: MSigDB Geneset - GSE26928_NAIVE_VS_CENT_MEMORY_CD4_TCELL_UP
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Mouse GO 274 Genes GS180521: GO:0000323 lytic vacuole
Expand Tier I Mouse MP 2915 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Mouse DRG 1131 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Human 2330 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse MP 36 Genes GS163976: MP:0006082 CNS inflammation
Expand Tier I Human GO 4136 Genes GS200341: GO:0051179 localization
Expand Tier I Mouse 191 Genes GS227636: MSigDB Geneset - GSE7852_LN_VS_THYMUS_TCONV_DN
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier III Fly 2223 Genes GS75562: Differentially expressed alcohol sensitivity in Drosophila melanogaster (line)
Expand Tier I Mouse MP 445 Genes GS165361: MP:0004624 abnormal thoracic cage morphology
Expand Tier II Mouse 460 Genes GS35733: Hippocampus Gene expression correlates of Open Field locomotion (cm) 0-15 min post cocaine in Males BXD
Expand Tier I Mouse CTD 844 Genes GS260212: sodium arsenate interacting with Mus musculus associated genes (MeSH:C009277) in CTD
Expand Tier I Mouse MP 790 Genes GS168336: MP:0000367 abnormal coat/ hair morphology
Expand Tier I Mouse MP 277 Genes GS168592: MP:0003634 abnormal glial cell morphology
Expand Tier I Mouse MP 1027 Genes GS165535: MP:0005370 liver/biliary system phenotype
Expand Tier I Mouse MP 842 Genes GS169774: MP:0001846 increased inflammatory response
Expand Tier I Mouse MP 1254 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier II Mouse 224 Genes GS135610: circulating hormone level QTL 2 (Chlq2, Published QTL Chr 3)
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Mouse 229 Genes GS136352: novelty/stress induced locomotor activation 2 (Nsila2, Published QTL Chr 3)
Expand Tier I Mouse GO 3209 Genes GS192509: GO:0006810 transport
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Mouse MP 807 Genes GS166862: MP:0000689 abnormal spleen morphology
Expand Tier II Human 679 Genes GS243748: [MeSH] Metabolism, Inborn Errors : D008661
Expand Tier II Mouse 458 Genes GS35718: Hippocampus Gene expression correlates of Open Field locomotion 0-15 min post cocaine in Males BXD
Expand Tier I Mouse MP 2315 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier I Human 87 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Mouse MP 1471 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier II Human 623 Genes GS236928: [MeSH] Lysosomes : D008247
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 889 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier II Human 2389 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier II Human 10111 Genes GS235272: [MeSH] Membrane Proteins : D008565
Expand Tier I Human 171 Genes GS230007: MSigDB Geneset - GCM_RAB10
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 511 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse MP 689 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Mouse 194 Genes GS229957: MSigDB Geneset - GSE13306_RA_VS_UNTREATED_TCONV_UP
Expand Tier I Mouse MP 133 Genes GS168473: MP:0002183 gliosis
Expand Tier I Mouse MP 16 Genes GS164021: MP:0006243 impaired pupillary reflex
Expand Tier I Mouse MP 640 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier I Mouse GO 8142 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 292 Genes GS228639: MSigDB Geneset - GCM_NF2
Expand Tier II Mouse 120 Genes GS35392: Hippocampus Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold in Males BXD
Expand Tier II Human 14403 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 77 Genes GS171254: HP:0002360 Sleep disturbance
Expand Tier I Human GO 7725 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 34 Genes GS172848: HP:0000488 Retinopathy
Expand Tier I Mouse MP 346 Genes GS169129: MP:0002446 abnormal macrophage morphology
Expand Tier II Human 1555 Genes GS243535: [MeSH] Neurodegenerative Diseases : D019636
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12781 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse MP 251 Genes GS167928: MP:0010630 abnormal cardiac muscle tissue morphology
Expand Tier I Mouse MP 790 Genes GS169303: MP:0008250 abnormal myeloid leukocyte morphology
Expand Tier II Mouse 244 Genes GS136625: Stem cell proliferation 6 (Scpro6, Published QTL Chr 3)
Expand Tier II Human 14645 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse MP 1983 Genes GS167542: MP:0001790 abnormal immune system physiology
Expand Tier II Human 12777 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier I Human 26 Genes GS176290: HP:0002123 Generalized myoclonic seizures
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Mouse MP 909 Genes GS165869: MP:0002138 abnormal hepatobiliary system 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 Mouse MP 735 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse 189 Genes GS228837: MSigDB Geneset - GSE14308_TH2_VS_INDUCED_TREG_UP
Expand Tier I Mouse 195 Genes GS227774: MSigDB Geneset - GSE27786_LIN_NEG_VS_NKTCELL_DN
Expand Tier I Human 84 Genes GS227866: MSigDB Geneset - GCM_BMPR2
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Human 50 Genes GS172258: HP:0002197 Generalized seizures
Expand Tier II Human 326 Genes GS241511: [MeSH] Lipid Metabolism Disorders : D052439
Expand Tier I Mouse CTD 10652 Genes GS256287: Tetrachlorodibenzodioxin interacting with Mus musculus associated genes (MeSH:D013749) in CTD
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 II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Human 9704 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 427 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier I Human CTD 228 Genes GS123337: Oxyquinoline interacting with Homo sapiens associated genes (MeSH:D015125) in CTD
Expand Tier I Mouse MP 40 Genes GS164163: MP:0005058 abnormal lysosome morphology
Expand Tier I Mouse MP 2672 Genes GS169767: MP:0002396 abnormal hematopoietic system morphology/development
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 I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 1684 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 182 Genes GS209175: GO:0005774 vacuolar membrane
Expand Tier I Human 514 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Mouse MP 793 Genes GS166513: MP:0008195 abnormal professional antigen presenting cell morphology
Expand Tier II Mouse 247 Genes GS84146: METH responses for home cage activity (Published QTL, Chr 3)
Expand Tier I Mouse 190 Genes GS228781: MSigDB Geneset - GSE27786_NKCELL_VS_NEUTROPHIL_UP
Expand Tier II Mouse 230 Genes GS136420: platelet activation 1 (Pact1, Published QTL Chr 3)
Expand Tier I Mouse MP 987 Genes GS165798: MP:0005367 renal/urinary system phenotype
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 Mouse MP 113 Genes GS168472: MP:0002182 abnormal astrocyte morphology
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human CTD 7249 Genes GS123768: Cyclosporine interacting with Homo sapiens associated genes (MeSH:D016572) in CTD
Expand Tier I Mouse MP 139 Genes GS170674: MP:0000278 abnormal myocardial fiber morphology
Expand Tier I Human 918 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Mouse MP 39 Genes GS165815: MP:0008918 microgliosis
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 167 Genes GS228251: MSigDB Geneset - GCM_MAP4K4
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier I Human GO 2363 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 894 Genes GS228513: MSigDB Geneset - RCGCANGCGY_V$NRF1_Q6
Expand Tier I Human GO 138 Genes GS206073: GO:0005765 lysosomal membrane
Expand Tier I Mouse MP 2319 Genes GS169829: MP:0005385 cardiovascular system phenotype
Expand Tier I Mouse MP 1419 Genes GS166250: MP:0008247 abnormal mononuclear cell morphology
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 257 Genes GS232648: PC Geneset - "V$ERR1_Q2" pathway genes
Expand Tier I Human 107 Genes GS176797: HP:0001268 Mental deterioration
Expand Tier I Human GO 14550 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6081 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier II Mouse 229 Genes GS135328: arthropathy in MRL and DBA/1 mice 2 (Artmd2, Published QTL Chr 3)
Expand Tier I Mouse GO 3266 Genes GS177721: GO:0051234 establishment of localization
Expand Tier I Mouse CTD 1485 Genes GS259234: propiconazole interacting with Mus musculus associated genes (MeSH:C045950) in CTD
Expand Tier I Mouse MP 26 Genes GS167773: MP:0002638 abnormal pupillary reflex
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Mouse MP 1583 Genes GS165465: MP:0003633 abnormal nervous system physiology
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Human 387 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier II Mouse 351 Genes GS26280: Hippocampus Gene expression correlates of Mechanical Sensitivity-Von Frey Threshold in Females & Males BXD
Expand Tier I Human 173 Genes GS228607: MSigDB Geneset - GSE29615_CTRL_VS_DAY3_LAIV_IFLU_VACCINE_PBMC_DN
Expand Tier I Human GO 251 Genes GS205611: GO:0044437 vacuolar part
Expand Tier I Mouse MP 1693 Genes GS168422: MP:0000716 abnormal immune system cell morphology
Expand Tier I Mouse MP 1084 Genes GS163818: MP:0002722 abnormal immune system organ morphology
Expand Tier I Human 899 Genes GS232228: PC Geneset - "RCGCANGCGY_V$NRF1_Q6" pathway genes
Expand Tier I Mouse MP 74 Genes GS166393: MP:0003354 astrocytosis
Expand Tier I Mouse MP 130 Genes GS167461: MP:0002792 abnormal retinal vasculature morphology
Expand Tier II Mouse 448 Genes GS34322: Hippocampus Gene expression correlates of Cocaine TOTAL locomotion (activity beam breaks) in Males BXD
Expand Tier III Mouse 77 Genes GS216888: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of heterogeneous stock (HS) mice short term selected lines. Light cyan Cluster
Expand Tier II Human 9375 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Mouse MP 1105 Genes GS166719: MP:0010678 abnormal skin adnexa morphology
Expand Tier II Mouse 451 Genes GS34005: Hippocampus Gene expression correlates of Open Field locomotion 15-30 min post cocaine in Males BXD
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
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 Human 97 Genes GS175976: HP:0003621 Juvenile onset
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Mouse MP 1961 Genes GS168149: MP:0005508 abnormal skeleton morphology
Expand Tier I Human GO 1686 Genes GS203755: GO:0016265 death
Expand Tier I Mouse CTD 10652 Genes GS256288: Tetracaine interacting with Mus musculus associated genes (MeSH:D013748) in CTD
Expand Tier I Mouse MP 1731 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Mouse MP 3063 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Mouse MP 1143 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human CTD 1026 Genes GS126265: Diazinon interacting with Homo sapiens associated genes (MeSH:D003976) in CTD
Expand Tier I Mouse GO 13185 Genes GS182834: GO:0005623 cell
Expand Tier I Human GO 5367 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Mouse MP 1019 Genes GS169773: MP:0001845 abnormal inflammatory response
Expand Tier I Mouse MP 2061 Genes GS169530: MP:0005390 skeleton phenotype
Expand Tier I Mouse GO 5246 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human GO 12490 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 251 Genes GS230812: MSigDB Geneset - V$ERR1_Q2
Expand Tier I Mouse MP 579 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier I Mouse MP 302 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier III Mouse 7391 Genes GS213076: Genes with suggestive difference in (C57BL/6) vs [(C57BL/6 x PWD)F1 + (PWD x C57BL/6)F1 + PWD] comparison
Expand Tier I Mouse MP 386 Genes GS169080: MP:0002075 abnormal coat/hair pigmentation
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Mouse MP 1870 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Mouse MP 209 Genes GS167917: MP:0000952 abnormal CNS glial cell morphology
Expand Tier I Human 11971 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Human GO 14517 Genes GS196941: GO:0008150 biological_process
Expand Tier II Mouse 252 Genes GS84145: high-dose ethanol actions (Published QTL, Chr 3)
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 I Mouse MP 753 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier II Human 9296 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier I Mouse 192 Genes GS228240: MSigDB Geneset - GSE17721_LPS_VS_CPG_1H_BMDM_UP
Expand Tier I Human GO 342 Genes GS197314: GO:0000323 lytic vacuole
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human GO 6349 Genes GS201256: GO:0044422 organelle part
Expand Tier II Human 3422 Genes GS235729: [MeSH] Membrane Transport Proteins : D026901
Expand Tier II Mouse 445 Genes GS35748: Hippocampus Gene expression correlates of Open Field locomotion (activity beam breaks) 0-15 min post 2nd cocaine in Males BXD
Expand Tier I Mouse 192 Genes GS228090: MSigDB Geneset - GSE31082_DN_VS_CD4_SP_THYMOCYTE_DN
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 GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier II Human 2446 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9519 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle