Gene Details



FKRP and homologs in 7 species are found in 963 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 969 Genes GS136900: ventral midbrain iron content 4 (Vmbic4, Published QTL Chr 7)
Expand Tier I Human 6 Genes GS176048: HP:0002359 Frequent falls
Expand Human 1715 Genes GS221148: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Mouse MP 175 Genes GS163171: MP:0000854 abnormal cerebellum development
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Mouse MP 15 Genes GS166439: MP:0006221 optic nerve hypoplasia
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Human 1715 Genes GS221397: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier II Human 12421 Genes GS239540: [MeSH] Heterochromatin : D006570
Expand Tier II Human 225 Genes GS245709: [MeSH] Dystrophin-Associated Proteins : D049029
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 I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Mouse 649 Genes GS135346: Avp transcript abundance QTL 1 (Avptaq1, Published QTL Chr 7)
Expand Tier I Human 194 Genes GS228344: MSigDB Geneset - GSE3982_BCELL_VS_EFF_MEMORY_CD4_TCELL_DN
Expand Tier I Mouse MP 30 Genes GS168741: MP:0009415 skeletal muscle degeneration
Expand Tier II Human 12069 Genes GS237417: [MeSH] Multigene Family : D005810
Expand Tier II Human 1599 Genes GS245714: [MeSH] Face : D005145
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Human 191 Genes GS229236: MSigDB Geneset - GSE17974_2H_VS_72H_UNTREATED_IN_VITRO_CD4_TCELL_UP
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier II Human 10106 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier I Human 17 Genes GS172643: HP:0002365 Hypoplasia of the brainstem
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human 769 Genes GS231653: PC Geneset - "CAGGTA_V$AREB6_01" pathway genes
Expand Tier III Rat 1082 Genes GS223255: Bone structure and strength QTL 66 (Bss66 Published QTL Chr 1)
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Mouse MP 36 Genes GS168493: MP:0010090 increased circulating creatine kinase level
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier III Rat 1082 Genes GS224178: Bone structure and strength QTL 69 (Bss69 Published QTL Chr 1)
Expand Tier I Human 167 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier II Human 446 Genes GS245783: [MeSH] Genetic Diseases, X-Linked : D040181
Expand Tier I Mouse GO 114 Genes GS186286: GO:0016485 protein processing
Expand Tier I Human 187 Genes GS229082: MSigDB Geneset - GSE15659_NONSUPPRESSIVE_TCELL_VS_ACTIVATED_TREG_UP
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 198 Genes GS228069: MSigDB Geneset - GSE29618_PRE_VS_DAY7_POST_LAIV_FLU_VACCINE_PDC_DN
Expand Tier I Mouse MP 371 Genes GS165643: MP:0011088 partial neonatal lethality
Expand Tier I Mouse MP 742 Genes GS165992: MP:0008469 abnormal protein level
Expand Tier II Human 616 Genes GS234799: [MeSH] Cardiomegaly : D006332
Expand Tier III Rat 1082 Genes GS224505: Bone structure and strength QTL 68 (Bss68 Published QTL Chr 1)
Expand Tier III Rat 766 Genes GS224576: Estrogen-induced pituitary tumorigenesis QTL 13 (Ept13 Published QTL Chr 1)
Expand Tier I Mouse MP 245 Genes GS165839: MP:0009701 abnormal birth body size
Expand Tier II Human 14581 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 851 Genes GS203972: GO:0005615 extracellular space
Expand Tier III Fly 2415 Genes GS213271: Head and thorax heatmapping of Canton-S fruit flies with dietary restrictions
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 65 Genes GS229839: MSigDB Geneset - GATGKMRGCG_UNKNOWN
Expand Tier I Human 198 Genes GS230487: MSigDB Geneset - GSE29618_PRE_VS_DAY7_FLU_VACCINE_PDC_DN
Expand Tier III Rat 710 Genes GS223738: Renal function QTL 29 (Rf29 Published QTL Chr 1)
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier II Human 1807 Genes GS238780: [MeSH] Head : D006257
Expand Tier I Human 16 Genes GS173830: HP:0002913 Myoglobinuria
Expand Tier II Mouse 92 Genes GS35700: Whole Brain Gene expression correlates of Morphine distance (cm) travelled minutes 105-120 in Females BXD
Expand Human 195 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier II Human 293 Genes GS236762: [MeSH] Nuclear Family : D009679
Expand Tier II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse MP 361 Genes GS167214: MP:0005319 abnormal enzyme/ coenzyme level
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 120 Genes GS203131: GO:0016485 protein processing
Expand Tier I Mouse 198 Genes GS229591: MSigDB Geneset - GSE27786_NKCELL_VS_ERYTHROBLAST_UP
Expand Tier I Human 257 Genes GS231926: PC Geneset - "V$POU3F2_02" pathway genes
Expand Tier III Rat 1482 Genes GS224475: Bone structure and strength QTL 54 (Bss54 Published QTL Chr 1)
Expand Tier I Mouse MP 781 Genes GS170024: MP:0011086 partial postnatal lethality
Expand Tier II Human 8197 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier I Human 19 Genes GS176247: HP:0002948 Vertebral fusion
Expand Tier I Mouse MP 1246 Genes GS165228: MP:0005382 craniofacial phenotype
Expand Tier I Mouse MP 38 Genes GS163906: MP:0009772 abnormal retinal development
Expand Tier I Human 9 Genes GS172223: HP:0001771 Achilles tendon contracture
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier I Mouse 969 Genes GS136531: prion resistance 2 (Prnr2, Published QTL Chr 7)
Expand Tier III Mouse 1046 Genes GS213200: Expression changes in the regulation of memory consolidation and synaptic function in FoxO6 vs. wild-type mice
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier III Fly 2417 Genes GS213272: Head and thorax heatmapping of reservatrol treated Canton-S fruit flies
Expand Tier I Human 196 Genes GS230507: MSigDB Geneset - GSE10325_CD4_TCELL_VS_LUPUS_CD4_TCELL_UP
Expand Tier I Human 90 Genes GS230145: MSigDB Geneset - KMCATNNWGGA_UNKNOWN
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Mouse MP 113 Genes GS164129: MP:0001573 abnormal circulating alanine transaminase level
Expand Tier I Mouse GO 122 Genes GS193053: GO:0051604 protein maturation
Expand Tier II Human 4022 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier II Human 18727 Genes GS236759: [MeSH] Intranuclear Space : D042581
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Mouse MP 2070 Genes GS163824: MP:0001259 abnormal body weight
Expand Tier I Mouse MP 503 Genes GS166591: MP:0004087 abnormal muscle fiber morphology
Expand Tier I Human 200 Genes GS230020: MSigDB Geneset - GSE13484_UNSTIM_VS_12H_YF17D_VACCINE_STIM_PBMC_DN
Expand Tier I Mouse MP 368 Genes GS163926: MP:0004097 abnormal cerebellar cortex morphology
Expand Tier I Mouse MP 323 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier II Human 3165 Genes GS235939: [MeSH] Cerebral Cortex : D002540
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 68 Genes GS176437: HP:0002334 Abnormality of the cerebellar vermis
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Human 84 Genes GS227473: MSigDB Geneset - CCAWNWWNNNGGC_UNKNOWN
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 I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier II Human 203 Genes GS243911: [MeSH] Respiration Disorders : D012120
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human 46 Genes GS173882: HP:0001305 Dandy-Walker malformation
Expand Tier I Human 7 Genes GS176546: HP:0003724 Shoulder girdle muscle atrophy
Expand Tier I Mouse 980 Genes GS135458: bone mineral density 4 (Bomd4, Published QTL Chr 7)
Expand Tier I Mouse MP 63 Genes GS170695: MP:0002699 abnormal vitreous body morphology
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 178 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier II Human 252 Genes GS241238: [MeSH] Muscular Dystrophies : D009136
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human 4 Genes GS174255: HP:0007033 Cerebellar dysplasia
Expand Tier I Human 22 Genes GS172190: HP:0002187 Intellectual disability, profound
Expand Tier II Human 5111 Genes GS242217: [MeSH] Muscle Proteins : D009124
Expand Tier I Mouse 197 Genes GS229650: MSigDB Geneset - GSE36392_TYPE_2_MYELOID_VS_EOSINOPHIL_IL25_TREATED_LUNG_UP
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
Expand Tier I Human 188 Genes GS230517: MSigDB Geneset - GSE15659_NAIVE_VS_PTPRC_NEG_CD4_TCELL_UP
Expand Tier I Mouse MP 1052 Genes GS166409: MP:0002114 abnormal axial skeleton morphology
Expand Tier I Human 250 Genes GS227414: MSigDB Geneset - V$TAL1BETAITF2_01
Expand Tier II Human 5908 Genes GS234387: [MeSH] Movement : D009068
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 10 Genes GS176947: HP:0006829 Severe muscular hypotonia
Expand Tier I Human 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Mouse MP 85 Genes GS165143: MP:0003733 abnormal retinal inner nuclear layer morphology
Expand Tier II Human 2418 Genes GS238560: [MeSH] Muscle Cells : D032342
Expand Tier I Mouse GO 17 Genes GS177768: GO:0016010 dystrophin-associated glycoprotein complex
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 18300 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier I Human 272 Genes GS227620: MSigDB Geneset - V$RFX1_02
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human GO 547 Genes GS205302: GO:0000139 Golgi membrane
Expand Tier II Human 253 Genes GS243468: [MeSH] Muscular Disorders, Atrophic : D020966
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 Human 65 Genes GS174481: HP:0010576 Intracranial cystic lesion
Expand Tier I Human 17 Genes GS175676: HP:0007362 Aplasia/Hypoplasia of the brainstem
Expand Tier I Mouse 199 Genes GS229507: MSigDB Geneset - GSE36392_TYPE_2_MYELOID_VS_MAC_IL25_TREATED_LUNG_DN
Expand Tier II Human 7284 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier I Human 240 Genes GS228713: MSigDB Geneset - V$AP2ALPHA_01
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Human 63 Genes GS221226: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier I Human 37 Genes GS172993: HP:0001321 Cerebellar hypoplasia
Expand Tier I Human 5 Genes GS176928: HP:0003741 Congenital muscular dystrophy
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human 122 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Mouse MP 463 Genes GS163429: MP:0000849 abnormal cerebellum morphology
Expand Tier II Human 1068 Genes GS241376: [MeSH] Sulfhydryl Compounds : D013438
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Mouse MP 1928 Genes GS166590: MP:0002873 normal phenotype
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse GO 228 Genes GS185668: GO:0009100 glycoprotein metabolic process
Expand Tier I Human 87 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 20 Genes GS168736: MP:0009412 skeletal muscle fiber degeneration
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human 196 Genes GS227738: MSigDB Geneset - GSE17974_2.5H_VS_72H_IL4_AND_ANTI_IL12_ACT_CD4_TCELL_UP
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 24 Genes GS176061: HP:0002355 Difficulty walking
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Mouse MP 1430 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse MP 3051 Genes GS163601: MP:0002089 abnormal postnatal growth/weight/body size
Expand Tier I Mouse MP 352 Genes GS167360: MP:0002200 abnormal brain ventricle/choroid plexus morphology
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 4413 Genes GS239859: [MeSH] Prosencephalon : D016548
Expand Tier II Mouse 90 Genes GS35535: Whole Brain Gene expression correlates of Morphine photocell counts minutes 105-120 in Females BXD
Expand Human 1715 Genes GS219769: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Mouse MP 628 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier I Mouse MP 35 Genes GS164038: MP:0003852 skeletal muscle necrosis
Expand Tier I Human 108 Genes GS227987: MSigDB Geneset - GTTGNYNNRGNAAC_UNKNOWN
Expand Tier II Mouse 155 Genes GS36597: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Males BXD
Expand Tier I Mouse MP 230 Genes GS163662: MP:0005277 abnormal brainstem morphology
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Mouse MP 3761 Genes GS165527: MP:0005378 growth/size phenotype
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier II Human 8645 Genes GS234354: [MeSH] Cytoskeletal Proteins : D003598
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier II Mouse 82 Genes GS36589: Striatum Gene expression correlates of Morphine vertical activity counts minutes 90-105 in Females BXD
Expand Tier II Human 2517 Genes GS246018: [MeSH] Heart Diseases : D006331
Expand Tier I Human 242 Genes GS227114: MSigDB Geneset - V$NFMUE1_Q6
Expand Tier I Human 20 Genes GS171252: HP:0003819 Death in childhood
Expand Tier I Mouse MP 472 Genes GS164448: MP:0005193 abnormal anterior eye segment morphology
Expand Tier I Mouse MP 239 Genes GS169262: MP:0003084 abnormal skeletal muscle fiber morphology
Expand Tier I Human 258 Genes GS228753: MSigDB Geneset - TTAYRTAA_V$E4BP4_01
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse 589 Genes GS136894: ventricular size 3 (Vent3, Published QTL Chr 7)
Expand Tier II Human 1240 Genes GS238245: [MeSH] Cerebellum : D002531
Expand Tier III Rat 713 Genes GS224074: Bone structure and strength QTL 87 (Bss87 Published QTL Chr 1)
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier II Human 2272 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Human 266 Genes GS232204: PC Geneset - "V$RFX1_02" pathway genes
Expand Tier I Human 270 Genes GS232636: PC Geneset - "V$AREB6_01" pathway genes
Expand Tier III Rat 743 Genes GS224213: Bone structure and strength QTL 94 (Bss94 Published QTL Chr 1)
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse MP 37 Genes GS166561: MP:0003648 abnormal radial glial cell morphology
Expand Tier I Mouse GO 785 Genes GS187113: GO:0005615 extracellular space
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane 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 91 Genes GS198475: GO:0042383 sarcolemma
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 GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Human 63 Genes GS219618: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier III Rat 707 Genes GS224383: Body weight QTL 29 (Bw29 Published QTL Chr 1)
Expand Tier III Rat 1482 Genes GS224478: Bone structure and strength QTL 53 (Bss53 Published QTL Chr 1)
Expand Tier I Mouse GO 186 Genes GS185669: GO:0009101 glycoprotein biosynthetic process
Expand Tier II Human 106 Genes GS237188: [MeSH] Phosphotransferases (Nitrogenous Group Acceptor) : D017852
Expand Tier II Human 19354 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
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 I Human CTD 4424 Genes GS123718: Ethinyl Estradiol interacting genes (MeSH:D004997) in CTD
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 81 Genes GS171773: HP:0000532 Chorioretinal abnormality
Expand Tier I Mouse 897 Genes GS135415: bronchial hyperresponsiveness 6 (Bhr6, Published QTL Chr 7)
Expand Tier I Human 92 Genes GS171656: HP:0000610 Abnormality of the choroid
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 147 Genes GS228847: MSigDB Geneset - BMI1_DN.V1_UP
Expand Tier I Mouse MP 2788 Genes GS167020: MP:0003956 abnormal body size
Expand Tier I Mouse MP 47 Genes GS170191: MP:0008511 thin retinal inner nuclear layer
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Mouse MP 1548 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Human GO 321 Genes GS202501: GO:0009101 glycoprotein biosynthetic process
Expand Tier III Rat 734 Genes GS224623: Serum cholesterol level QTL 6 (Scl6 Published QTL Chr 1)
Expand Tier I Mouse MP 112 Genes GS163174: MP:0000857 abnormal cerebellar foliation
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse 198 Genes GS228192: MSigDB Geneset - GSE32423_IL7_VS_IL7_IL4_MEMORY_CD8_TCELL_DN
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse MP 1674 Genes GS169530: MP:0005390 skeleton phenotype
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 5399 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier II Human 10298 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier II Human 15731 Genes GS236183: [MeSH] Chromosome Structures : D022004
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 8 Genes GS174113: HP:0008981 Calf muscle hypertrophy
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Mouse MP 481 Genes GS163292: MP:0003091 abnormal cell migration
Expand Tier III Rat 1641 Genes GS223264: Neuroinflammation QTL 8 (Neuinf8 Published QTL Chr 1)
Expand Tier I Human 191 Genes GS228940: MSigDB Geneset - GSE3982_MAST_CELL_VS_EFF_MEMORY_CD4_TCELL_DN
Expand Tier II Human 5285 Genes GS238828: [MeSH] Locomotion : D008124
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier II Human 2194 Genes GS235041: [MeSH] Glycosyltransferases : D016695
Expand Tier I Mouse MP 378 Genes GS167917: MP:0000952 abnormal CNS glial cell 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 GO 57 Genes GS186812: GO:0005791 rough endoplasmic reticulum
Expand Tier I Human 225 Genes GS232319: PC Geneset - "V$PU1_Q6" pathway genes
Expand Tier III Rat 1758 Genes GS223048: Hepatocarcinoma susceptibility QTL 2 (Hcas2 Published QTL Chr 1)
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
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 GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse MP 286 Genes GS170158: MP:0000074 abnormal neurocranium morphology
Expand Tier I Mouse MP 92 Genes GS166794: MP:0002941 increased circulating alanine transaminase level
Expand Tier III Rat 710 Genes GS223509: Serum renin concentration QTL 4 (Srn4 Published QTL Chr 1)
Expand Tier II Human 15607 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Human 63 Genes GS220977: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier II Human 499 Genes GS235763: [MeSH] Chromosomes, Human, Pair 19 : D002888
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier III Rat 2769 Genes GS223189: Non-insulin dependent diabetes mellitus QTL 44 (Niddm44 Published QTL Chr 1)
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier II Human 189 Genes GS243247: [MeSH] Cardiomyopathy, Dilated : D002311
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 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 98 Genes GS171910: HP:0003828 Variable expressivity
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
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 Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier III Rat 921 Genes GS223673: Pristane induced arthritis QTL 36 (Pia36 Published QTL Chr 1)
Expand Tier III Rat 750 Genes GS223734: Renal function QTL 27 (Rf27 Published QTL Chr 1)
Expand Tier II Human 1294 Genes GS234220: [MeSH] Metencephalon : D020540
Expand Tier I Human 32 Genes GS171753: HP:0001712 Left ventricular hypertrophy
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 Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
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 588 Genes GS235755: [MeSH] Cardiomyopathies : D009202
Expand Tier II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier II Human 2118 Genes GS236633: [MeSH] Brain Stem : D001933
Expand Tier II Human 10952 Genes GS241962: [MeSH] RNA Interference : D034622
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 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Mouse MP 832 Genes GS167759: MP:0000787 abnormal telencephalon morphology
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier III Rat 1482 Genes GS223648: Bone structure and strength QTL 58 (Bss58 Published QTL Chr 1)
Expand Tier I Human 8 Genes GS171731: HP:0003547 Shoulder girdle muscle weakness
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Mouse 969 Genes GS136264: modifier of mammary tumor progression 1 (Mmtp1, Published QTL Chr 7)
Expand Tier I Mouse MP 108 Genes GS169489: MP:0000747 muscle weakness
Expand Tier III Human 1850 Genes GS246376: H3K4me3 CHiP Seq Hippocampi Human Cocaine Addicts
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier II Human 4765 Genes GS236201: [MeSH] Embryonic Stem Cells : D053595
Expand Tier I Mouse MP 7 Genes GS169879: MP:0010235 abnormal retina inner limiting membrane morphology
Expand Tier I Mouse MP 635 Genes GS164032: MP:0004811 abnormal neuron physiology
Expand Tier I Mouse MP 3396 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier II Mouse 89 Genes GS34349: Striatum Gene expression correlates of Morphine Open Field TOTAL distance (cm) travelled in Females & Males BXD
Expand Tier II Human 3887 Genes GS238322: [MeSH] Behavior and Behavior Mechanisms : D001520
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier II Human 4020 Genes GS237150: [MeSH] Eye : D005123
Expand Tier II Human 2858 Genes GS244661: [MeSH] Muscle, Skeletal : D018482
Expand Tier I Mouse MP 34 Genes GS168743: MP:0009419 skeletal muscle fibrosis
Expand Tier I Mouse MP 1925 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 35 Genes GS173690: HP:0001644 Dilated cardiomyopathy
Expand Tier I Human GO 1166 Genes GS201075: GO:0005794 Golgi apparatus
Expand Tier I Mouse MP 229 Genes GS170688: MP:0002697 abnormal eye size
Expand Tier II Human 15426 Genes GS239526: [MeSH] Phosphotransferases : D010770
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 231 Genes GS229563: MSigDB Geneset - V$PU1_Q6
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1718 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human GO 20 Genes GS194508: GO:0016010 dystrophin-associated glycoprotein complex
Expand Tier I Human 47 Genes GS172604: HP:0005445 Widened posterior fossa
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier II Human 3010 Genes GS241608: [MeSH] Haplotypes : D006239
Expand Tier I Mouse MP 105 Genes GS167442: MP:0000440 domed cranium
Expand Tier I Mouse GO 1440 Genes GS181988: GO:0044459 plasma membrane part
Expand Tier I Mouse MP 172 Genes GS165640: MP:0002269 muscular atrophy
Expand Tier I Mouse 827 Genes GS136263: modifier of mammary tumor growth 3 (Mmtg3, Published QTL Chr 7)
Expand Tier I Mouse MP 553 Genes GS167217: MP:0001325 abnormal retina morphology
Expand Tier I Human 17 Genes GS173239: HP:0001339 Lissencephaly
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier II Human 30317 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Human 63 Genes GS220154: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier I Human 177 Genes GS228730: MSigDB Geneset - V$CREBP1_01
Expand Tier I Human GO 1202 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier I Human 248 Genes GS229410: MSigDB Geneset - V$AP2GAMMA_01
Expand Tier I Mouse MP 365 Genes GS164530: MP:0000801 abnormal temporal lobe morphology
Expand Tier I Mouse MP 139 Genes GS169804: MP:0003731 abnormal retinal outer nuclear layer morphology
Expand Tier I Mouse 200 Genes GS230411: MSigDB Geneset - GSE27786_ERYTHROBLAST_VS_MONO_MAC_DN
Expand Tier I Human 24 Genes GS174091: HP:0004327 Abnormality of the vitreous humor
Expand Tier I Human 252 Genes GS232440: PC Geneset - "TTAYRTAA_V$E4BP4_01" pathway genes
Expand Tier I Mouse MP 794 Genes GS169062: MP:0000913 abnormal brain development
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 Human 63 Genes GS222831: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 41 Genes GS172019: HP:0001360 Holoprosencephaly
Expand Tier I Mouse MP 338 Genes GS166450: MP:0011089 complete perinatal lethality
Expand Tier I Mouse MP 21 Genes GS166991: MP:0009414 skeletal muscle fiber necrosis
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 269 Genes GS230821: MSigDB Geneset - V$AREB6_01
Expand Tier II Mouse 98 Genes GS36602: Whole Brain Gene expression correlates of Morphine vertical activity counts minutes 105-120 in Females & Males BXD
Expand Tier I Human 373 Genes GS229420: MSigDB Geneset - AAAYRNCTG_UNKNOWN
Expand Tier I Human 37 Genes GS173880: HP:0005750 Contractures of the joints of the lower limbs
Expand Tier I Human 194 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 196 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Mouse MP 623 Genes GS164446: MP:0005195 abnormal posterior eye segment morphology
Expand Tier I Mouse 906 Genes GS135746: experimental allergic encephalomyelitis susceptibility 12 (Eae12, Published QTL Chr 7)
Expand Tier II Human 13886 Genes GS245484: [MeSH] Insect Proteins : D019476
Expand Tier I Human 816 Genes GS228126: MSigDB Geneset - chr19q13
Expand Tier II Human 3598 Genes GS238082: [MeSH] Fish Proteins : D029941
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse DRG 1196 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Human 26 Genes GS170797: HP:0003560 Muscular dystrophy
Expand Tier I Human 247 Genes GS231659: PC Geneset - "V$AP2GAMMA_01" pathway genes
Expand Tier I Mouse MP 51 Genes GS169180: MP:0000752 dystrophic muscle
Expand Tier I Mouse GO 1006 Genes GS184267: GO:0005794 Golgi apparatus
Expand Tier I Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier II Human 12246 Genes GS243456: [MeSH] Euchromatin : D022041
Expand Tier I Human 166 Genes GS229358: MSigDB Geneset - GTTRYCATRR_UNKNOWN
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 16 Genes GS176886: HP:0100261 Abnormal tendon morphology
Expand Tier I Human 18 Genes GS176941: HP:0002791 Hypoventilation
Expand Tier I Mouse MP 1415 Genes GS169531: MP:0005391 vision/eye phenotype
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Mouse MP 64 Genes GS168366: MP:0000109 abnormal parietal bone morphology
Expand Tier I Mouse MP 569 Genes GS165809: MP:0002864 abnormal ocular fundus morphology
Expand Tier II Human 9287 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
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 Mouse MP 4902 Genes GS165525: MP:0010768 mortality/aging
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 Tier I Mouse GO 362 Genes GS177764: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
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 III Rat 1082 Genes GS224794: Bone structure and strength QTL 70 (Bss70 Published QTL Chr 1)
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human 197 Genes GS228523: MSigDB Geneset - GSE3982_EFF_MEMORY_CD4_TCELL_VS_NKCELL_UP
Expand Tier II Human 12489 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier I Human 257 Genes GS227402: MSigDB Geneset - V$POU3F2_02
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier III Rat 1482 Genes GS224474: Bone structure and strength QTL 57 (Bss57 Published QTL Chr 1)
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Mouse 1020 Genes GS136253: modifier of Dlk1 (mdlk1, Published QTL Chr 7)
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 26 Genes GS173870: HP:0001302 Pachygyria
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Mouse 936 Genes GS136189: lipoprotein QTL 5 (Lprq5, Published QTL Chr 7)
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 198 Genes GS174812: HP:0001637 Abnormality of the myocardium
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 I Mouse MP 18 Genes GS163045: MP:0003083 abnormal tibialis anterior morphology
Expand Tier I Mouse MP 583 Genes GS165437: MP:0000438 abnormal cranium morphology
Expand Tier II Human 880 Genes GS237395: [MeSH] Muscle Fibers, Skeletal : D018485
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 97 Genes GS176756: HP:0011420 Death
Expand Tier I Mouse MP 357 Genes GS167748: MP:0000788 abnormal cerebral cortex morphology
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier II Human 1835 Genes GS239653: [MeSH] Social Sciences : D012942
Expand Tier II Human 34 Genes GS235114: [MeSH] Respiratory Insufficiency : D012131
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier II Human 18456 Genes GS243735: [MeSH] Biological Factors : D001685
Expand Tier I Human GO 549 Genes GS194503: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier II Human 8647 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier I Mouse MP 219 Genes GS162928: MP:0006108 abnormal hindbrain development
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Human GO 3239 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 246 Genes GS231934: PC Geneset - "V$TAL1BETAITF2_01" pathway genes
Expand Tier I Human 56 Genes GS176885: HP:0002693 Abnormality of the skull base
Expand Tier II Human 5596 Genes GS235557: [MeSH] Animal Diseases : D000820
Expand Tier I Human 1 Genes GS173745: HP:0005162 Impaired left ventricular function
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier II Human 14476 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier I Human 63 Genes GS175327: HP:0000568 Microphthalmos
Expand Tier II Human 141 Genes GS241777: [MeSH] Siblings : D035781
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier II Human 19667 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier II Human 2932 Genes GS236094: [MeSH] Scleroproteins : D012596
Expand Tier I Mouse MP 1698 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier II Human 174 Genes GS237392: [MeSH] Dystrophin : D016189
Expand Tier I Mouse MP 1039 Genes GS166120: MP:0002106 abnormal muscle physiology
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 I Mouse MP 86 Genes GS168450: MP:0009404 centrally nucleated skeletal muscle fibers
Expand Tier I Human 194 Genes GS229324: MSigDB Geneset - GSE3982_EFF_MEMORY_CD4_TCELL_VS_TH2_UP
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Human 63 Genes GS222079: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier I Mouse