Gene Details



SHOX and homologs in 4 species are found in 548 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 II Human 3883 Genes GS242641: [MeSH] Genes, Reporter : D017930
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 130 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier II Human 14476 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier II Human 19440 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier II Human 644 Genes GS244888: [MeSH] Heart Defects, Congenital : D006330
Expand Tier II Human 1106 Genes GS242659: [MeSH] Islands : D062312
Expand Tier II Human 6358 Genes GS238474: [MeSH] Hormones : D006728
Expand Tier II Human 6985 Genes GS238182: [MeSH] Oncogene Proteins : D015513
Expand Tier I Human 15 Genes GS171103: HP:0006492 Aplasia/Hypoplasia of the fibula
Expand Tier II Human 2438 Genes GS242599: [MeSH] Enhancer Elements, Genetic : D004742
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 II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier II Human 1699 Genes GS243051: [MeSH] Adnexa Uteri : D000290
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier II Human 6632 Genes GS241841: [MeSH] Genitalia : D005835
Expand Tier II Human 2440 Genes GS243677: [MeSH] Germ Layers : D005855
Expand Human 63 Genes GS222079: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 657 Genes GS243964: [MeSH] Chromosome Deletion : D002872
Expand Tier I Human 280 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier II Human 1685 Genes GS245086: [MeSH] Skeleton : D012863
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier II Human 962 Genes GS238428: [MeSH] Allelic Imbalance : D022981
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 1 Genes GS176448: HP:0006459 Dorsal subluxation of ulna
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 683 Genes GS238289: [MeSH] Cardiovascular Abnormalities : D018376
Expand Tier I Human 148 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier II Human 2923 Genes GS243816: [MeSH] Organogenesis : D038081
Expand Human 1733 Genes GS219981: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Human 31 Genes GS171877: HP:0002991 Abnormality of the fibula
Expand Human 2063 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier II Human 123 Genes GS236323: [MeSH] Receptor, Fibroblast Growth Factor, Type 3 : D051498
Expand Tier II Human 15224 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier II Human 3240 Genes GS236066: [MeSH] Musculoskeletal Physiological Phenomena : D009142
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier II Human 1090 Genes GS238558: [MeSH] Tandem Repeat Sequences : D020080
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Human 94 Genes GS219707: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_MATRIX
Expand Tier II Human 1663 Genes GS240024: [MeSH] Gene Dosage : D018628
Expand Tier II Human 495 Genes GS237845: [MeSH] Bone Diseases, Developmental : D001848
Expand Human 68 Genes GS222190: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_ARRHYTHMOGENIC_RIGHT_VENTRICULAR_CARDIOMYOPATHY_ARVC
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier II Human 30225 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Human 84 Genes GS219676: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_DILATED_CARDIOMYOPATHY
Expand Human 2063 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier II Human 2184 Genes GS241321: [MeSH] Untranslated Regions : D020506
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier II Human 1671 Genes GS241290: [MeSH] Ovary : D010053
Expand Human 2063 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human CTD 228 Genes GS127198: Carmustine interacting genes (MeSH:D002330) in CTD
Expand Tier II Human 3419 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier II Human 432 Genes GS236659: [MeSH] Codon, Terminator : D018388
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Human 51 Genes GS171286: HP:0002996 Limited elbow movement
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Human 6 Genes GS240491: [MeSH] Arm : D001132
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Human 34 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
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 II Human 7105 Genes GS239559: [MeSH] Oxidoreductases : D010088
Expand Human 1470 Genes GS219977: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 19 Genes GS172642: HP:0002982 Tibial bowing
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Human 84 Genes GS220953: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_DILATED_CARDIOMYOPATHY
Expand Tier I Human 49 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human 14 Genes GS176201: HP:0100777 Exostoses
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 7 Genes GS173432: HP:0010012 Abnormality of the 4th metacarpal
Expand Tier II Human 800 Genes GS237532: [MeSH] Extremities : D005121
Expand Tier II Human 7137 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Human 1733 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier II Human 9719 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier II Human 5015 Genes GS240747: [MeSH] Endocrine Glands : D004702
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 187 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier II Human 686 Genes GS241459: [MeSH] Psychology, Social : D011593
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 14842 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier II Human 4779 Genes GS245543: [MeSH] Receptors, Peptide : D018000
Expand Tier I Human 1 Genes GS175145: HP:0100745 Abnormality of the humeroulnar joint
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier I Human 10 Genes GS173531: HP:0005772 Aplasia/Hypoplasia of the tibia
Expand Tier I Human 20 Genes GS175698: HP:0003022 Hypoplasia of the ulna
Expand Tier II Human 21236 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier II Human 165 Genes GS239107: [MeSH] Dwarfism : D004392
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Human 2176 Genes GS235901: [MeSH] Mesoderm : D008648
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 1 Genes GS173236: HP:0003102 Increased carrying angle
Expand Tier II Human 1323 Genes GS243817: [MeSH] Abnormalities, Multiple : D000015
Expand Human 474 Genes GS219938: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier II Human 3807 Genes GS242661: [MeSH] Endocrine System Diseases : D004700
Expand Human 93 Genes GS219706: http://www.broadinstitute.org/gsea/msigdb/cards/PROTEINACEOUS_EXTRACELLULAR_MATRIX
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier II Human 2845 Genes GS244436: [MeSH] Gene Frequency : D005787
Expand Tier I Human 42 Genes GS171878: HP:0002992 Abnormality of the tibia
Expand Tier I Human 49 Genes GS172266: HP:0001191 Abnormality of the carpal bones
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 83 Genes GS171875: HP:0002997 Abnormality of the ulna
Expand Tier I Human 26 Genes GS176818: HP:0010622 Neoplasm of the skeletal system
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 6705 Genes GS234738: [MeSH] Proto-Oncogene Proteins : D011518
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 148 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human 197 Genes GS228625: MSigDB Geneset - GSE9006_HEALTHY_VS_TYPE_2_DIABETES_PBMC_AT_DX_DN
Expand Tier II Human 249 Genes GS234778: [MeSH] Growth Disorders : D006130
Expand Tier I Human 63 Genes GS175660: HP:0006501 Aplasia/Hypoplasia of the radius
Expand Tier I Human 5 Genes GS175975: HP:0010044 Short 4th metacarpal
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human 52 Genes GS172644: HP:0002981 Abnormality of the calf
Expand Tier II Human 145 Genes GS238794: [MeSH] Sexual and Gender Disorders : D019968
Expand Tier II Human 878 Genes GS243339: [MeSH] Musculoskeletal Abnormalities : D009139
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 9 Genes GS172493: HP:0003038 Fibular hypoplasia
Expand Tier I Human 10 Genes GS173229: HP:0005736 Hypoplastic tibia
Expand Tier II Human 4140 Genes GS235830: [MeSH] Cardiovascular Diseases : D002318
Expand Tier II Human 917 Genes GS243243: [MeSH] Pituitary Hormones, Anterior : D010908
Expand Tier I Human 392 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier II Human 1030 Genes GS242703: [MeSH] Ploidies : D011003
Expand Tier II Human 288 Genes GS235191: [MeSH] Y Chromosome : D014998
Expand Tier II Human 7543 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier I Human 77 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier II Human 2795 Genes GS245892: [MeSH] Musculoskeletal Diseases : D009140
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier II Human 2543 Genes GS243625: [MeSH] Sex Chromosomes : D012730
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human GO 1001 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier II Human 15 Genes GS243006: [MeSH] Sex Chromosome Disorders of Sex Development : D058533
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 2776 Genes GS237733: [MeSH] Mental Disorders : D001523
Expand Tier I Human 40 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier II Human 3887 Genes GS238322: [MeSH] Behavior and Behavior Mechanisms : D001520
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 12802 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Human 68 Genes GS222906: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_ARRHYTHMOGENIC_RIGHT_VENTRICULAR_CARDIOMYOPATHY_ARVC
Expand Tier II Human 71 Genes GS235059: [MeSH] Sex Chromosome Disorders : D025064
Expand Tier II Human 5058 Genes GS241605: [MeSH] Embryo, Nonmammalian : D004625
Expand Tier II Human 13659 Genes GS242677: [MeSH] Phosphotransferases (Alcohol Group Acceptor) : D017853
Expand Tier II Human 1432 Genes GS235231: [MeSH] Bone and Bones : D001842
Expand Tier II Human 10066 Genes GS238280: [MeSH] Cell Cycle : D002453
Expand Tier II Human 927 Genes GS238378: [MeSH] Chick Embryo : D002642
Expand Tier II Human 15426 Genes GS239526: [MeSH] Phosphotransferases : D010770
Expand Human 30 Genes GS221025: http://www.broadinstitute.org/gsea/msigdb/cards/BASEMENT_MEMBRANE
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier II Human 8635 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Human 94 Genes GS219924: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_MATRIX
Expand Tier I Human 28 Genes GS176426: HP:0003063 Abnormality of the humerus
Expand Tier II Human 5083 Genes GS244537: [MeSH] Protein-Tyrosine Kinases : D011505
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier II Human 2179 Genes GS236278: [MeSH] Chromosome Aberrations : D002869
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 8519 Genes GS243346: [MeSH] Chromosomes, Human : D002877
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier II Human 13250 Genes GS238537: [MeSH] Pharmacological Phenomena : D002620
Expand Tier II Human 700 Genes GS238897: [MeSH] Sociology : D012961
Expand Tier II Human 225 Genes GS243862: [MeSH] Osteochondrodysplasias : D010009
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier II Human 73890 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 29 Genes GS173982: HP:0001454 Abnormality of the upper arm
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier II Human 16067 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 77 Genes GS236296: [MeSH] Haploinsufficiency : D057895
Expand Tier II Human 13292 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier II Human 1155 Genes GS238243: [MeSH] Bone Diseases : D001847
Expand Tier II Human 849 Genes GS236202: [MeSH] Microsatellite Repeats : D018895
Expand Tier II Human 3010 Genes GS241608: [MeSH] Haplotypes : D006239
Expand Tier II Human 6078 Genes GS236700: [MeSH] Musculoskeletal System : D009141
Expand Tier II Human 253 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 22 Genes GS171098: HP:0006498 Aplasia/Hypoplasia of the patella
Expand Tier I Human GO 333 Genes GS196532: GO:0000975 regulatory region DNA binding
Expand Human 204 Genes GS222873: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_PLATELET_ACTIVATION_SIGNALING_AND_AGGREGATION
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Human 21 Genes GS172117: HP:0002984 Hypoplasia of the radius
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human 5 Genes GS174277: HP:0010042 Aplasia/Hypoplasia of the 4th metacarpal
Expand Tier II Human 480 Genes GS235824: [MeSH] 5' Untranslated Regions : D020121
Expand Tier II Human 18300 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier II Human 30317 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Human 1197 Genes GS219982: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Human 63 Genes GS220154: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier II Human 32 Genes GS234900: [MeSH] Sex Chromosome Aberrations : D012729
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier II Human 56931 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier I Human 123 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier II Human 30254 Genes GS243763: [MeSH] Intracellular Space : D042541
Expand Human 75 Genes GS219617: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_HYPERTROPHIC_CARDIOMYOPATHY_HCM
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier II Human 8112 Genes GS235286: [MeSH] Cell Death : D016923
Expand Human 474 Genes GS219721: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION
Expand Tier II Human 6475 Genes GS240223: [MeSH] Down-Regulation : D015536
Expand Tier II Human 297 Genes GS245370: [MeSH] Limb Deformities, Congenital : D017880
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human 93 Genes GS174308: HP:0002979 Bowing of the legs
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier II Human 3036 Genes GS241690: [MeSH] Female Urogenital Diseases : D052776
Expand Human 1470 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier II Human 13895 Genes GS244414: [MeSH] Arthropod Proteins : D060829
Expand Human 1197 Genes GS219942: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 66 Genes GS172588: HP:0001831 Short toe
Expand Human 63 Genes GS222831: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier II Human 37 Genes GS239099: [MeSH] Mullerian Ducts : D009095
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 II Human 325 Genes GS238765: [MeSH] Dosage Compensation, Genetic : D004303
Expand Tier II Human 6379 Genes GS241307: [MeSH] Hormones, Hormone Substitutes, and Hormone Antagonists : D006730
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier II Human 73218 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier II Human 2694 Genes GS235642: [MeSH] Body Regions : D001829
Expand Tier II Human 86 Genes GS237462: [MeSH] Genomic Structural Variation : D056914
Expand Tier II Human 3554 Genes GS244384: [MeSH] Female Urogenital Diseases and Pregnancy Complications : D005261
Expand Tier II Human 16797 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Human 54 Genes GS171298: HP:0002829 Arthralgia
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier II Human 7284 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 1 Genes GS176520: HP:0008845 Mesomelic short stature
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Human 2 Genes GS174079: HP:0002762 Multiple exostoses
Expand Tier I Human 11 Genes GS172115: HP:0002986 Radial bowing
Expand Tier I Human 21 Genes GS175859: HP:0006443 Patellar aplasia
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 12 Genes GS241894: [MeSH] Turner Syndrome : D014424
Expand Human 1197 Genes GS219725: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Human 45 Genes GS175084: HP:0008384 Aplastic/hypoplastic fingernail
Expand Tier II Human 194 Genes GS242840: [MeSH] Disorders of Sex Development : D012734
Expand Human 63 Genes GS221226: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier I Human 5 Genes GS172291: HP:0003067 Madelung deformity
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human 186 Genes GS230055: MSigDB Geneset - GSE17974_0H_VS_1H_IN_VITRO_ACT_CD4_TCELL_UP
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier II Human 3287 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier II Human 13886 Genes GS245484: [MeSH] Insect Proteins : D019476
Expand Tier II Human 666 Genes GS244425: [MeSH] Receptors, Fibroblast Growth Factor : D017468
Expand Tier II Human 6198 Genes GS244779: [MeSH] Embryonic and Fetal Development : D005314
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Human 642 Genes GS240790: [MeSH] Chondrocytes : D019902
Expand Tier II Human 35136 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Human 280 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier II Human 9754 Genes GS243806: [MeSH] Time : D013995
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Human 30 Genes GS219894: http://www.broadinstitute.org/gsea/msigdb/cards/BASEMENT_MEMBRANE
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 79 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier II Human 182 Genes GS235576: [MeSH] Growth Plate : D006132
Expand Human 30 Genes GS219677: http://www.broadinstitute.org/gsea/msigdb/cards/BASEMENT_MEMBRANE
Expand Tier I Human 58 Genes GS171822: HP:0000112 Nephropathy
Expand Tier II Human 86 Genes GS244957: [MeSH] DNA Copy Number Variations : D056915
Expand Tier I Human GO 325 Genes GS202371: GO:0044212 transcription regulatory region DNA binding
Expand Human 1733 Genes GS219987: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human GO 999 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier II Human 19302 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier II Human 35 Genes GS237629: [MeSH] Gonadal Dysgenesis : D006059
Expand Tier I Human 147 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier II Human 11662 Genes GS239443: [MeSH] RNA Splicing : D012326
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier II Human 8667 Genes GS234532: [MeSH] Sequence Deletion : D017384
Expand Tier I Human GO 333 Genes GS208604: GO:0001067 regulatory region nucleic acid binding
Expand Tier II Human 15356 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier II Human 15662 Genes GS235446: [MeSH] Reproductive and Urinary Physiological Phenomena : D012101
Expand Tier II Human 22746 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier II Human 2441 Genes GS234046: [MeSH] Genitalia, Female : D005836
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier II Human 16 Genes GS239239: [MeSH] Luciferases, Firefly : D049409
Expand Tier I Human 199 Genes GS230270: MSigDB Geneset - GSE360_CTRL_VS_B_MALAYI_LOW_DOSE_MAC_DN
Expand Tier II Human 760 Genes GS237355: [MeSH] Aneuploidy : D000782
Expand Tier II Human 1041 Genes GS239408: [MeSH] Pituitary Hormones : D010907
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier II Human 27720 Genes GS235272: [MeSH] Membrane Proteins : D008565
Expand Tier II Human 902 Genes GS240209: [MeSH] Uterus : D014599
Expand Tier I Human 96 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier II Human 48 Genes GS240183: [MeSH] Chromosomes, Human, Y : D041322
Expand Tier I Human 8 Genes GS175564: HP:0003027 Mesomelia
Expand Tier II Human 13521 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Human 184 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier II Human 268 Genes GS239950: [MeSH] Growth Hormone : D013006
Expand Human 68 Genes GS219626: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_ARRHYTHMOGENIC_RIGHT_VENTRICULAR_CARDIOMYOPATHY_ARVC
Expand Tier II Human 83 Genes GS233995: [MeSH] Human Growth Hormone : D019382
Expand Tier I Human 32 Genes GS172698: HP:0002653 Bone pain
Expand Tier II Human 9287 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier II Human 1813 Genes GS243764: [MeSH] Connective Tissue : D003238
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 54 Genes GS176473: HP:0003498 Disproportionate short stature
Expand Tier II Human 107 Genes GS241822: [MeSH] Haploidy : D006238
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
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 Human 138 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human 66 Genes GS172110: HP:0002983 Micromelia
Expand Tier I Human GO 3178 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier II Human 1872 Genes GS242635: [MeSH] Luciferases : D008156
Expand Tier II Human 8967 Genes GS239365: [MeSH] Pharmacological Processes : D055632
Expand Human 85 Genes GS222875: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_RESPONSE_TO_ELEVATED_PLATELET_CYTOSOLIC_CA2_
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 83 Genes GS172316: HP:0003026 Short long bones
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
Expand Human 2063 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Human 1470 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier II Human 960 Genes GS241012: [MeSH] Loss of Heterozygosity : D019656
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier II Human 659 Genes GS245028: [MeSH] Monosomy : D009006
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human 16 Genes GS170886: HP:0006488 Bowing of the arm
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier II Human 2477 Genes GS237394: [MeSH] Point Mutation : D017354
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier II Human 12085 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier I Human 356 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 60 Genes GS174139: HP:0005914 Aplasia/Hypoplasia involving the metacarpal bones
Expand Tier I Human 38 Genes GS172268: HP:0001193 Ulnar deviation of the hand or of fingers of the hand
Expand Tier I Human 121 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier II Human 904 Genes GS237234: [MeSH] Chromosomes, Human, 21-22 and Y : D002904
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 12489 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier II Human 1015 Genes GS245745: [MeSH] Chromosome Disorders : D025063
Expand Human 471 Genes GS222221: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_HEMOSTASIS
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 2 Genes GS173924: HP:0004986 Rudimentary to absent fibulae
Expand Tier I Human 116 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier II Human 3556 Genes GS234306: [MeSH] Receptors, Growth Factor : D017978
Expand Tier II Human 839 Genes GS238687: [MeSH] Disease : D004194
Expand Tier II Human 12369 Genes GS245348: [MeSH] RNA Processing, Post-Transcriptional : D012323
Expand Tier II Human 2517 Genes GS246018: [MeSH] Heart Diseases : D006331
Expand Tier I Human 280 Genes GS229012: MSigDB Geneset - KRAS.600.LUNG.BREAST_UP.V1_UP
Expand Tier II Human 15964 Genes GS237339: [MeSH] Regulatory Sequences, Nucleic Acid : D012045
Expand Tier II Human 393 Genes GS239233: [MeSH] Codon, Nonsense : D018389
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier II Human 821 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Human 47 Genes GS174089: HP:0003367 Abnormality of the femoral neck
Expand Tier I Human 85 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 110 Genes GS176480: HP:0009826 Hypoplasia involving bones of the extremities
Expand Tier I Human 1 Genes GS171181: HP:0006381 Rudimentary fibula
Expand Tier II Human 625 Genes GS243813: [MeSH] Family : D005190
Expand Tier II Human 12251 Genes GS237745: [MeSH] Epigenesis, Genetic : D044127
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier II Human 3054 Genes GS245998: [MeSH] Musculoskeletal Physiological Processes : D043702
Expand Tier I Human 54 Genes GS172140: HP:0002857 Genu valgum
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 15 Genes GS172482: HP:0003032 Short femoral neck
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier II Human 22498 Genes GS245206: [MeSH] Cell Nucleus : D002467
Expand Tier I Human 193 Genes GS227851: MSigDB Geneset - GSE9006_1MONTH_VS_4MONTH_POST_TYPE_1_DIABETES_DX_PBMC_DN
Expand Tier I Human 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier II Human 1803 Genes GS245900: [MeSH] Fetus : D005333
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 103 Genes GS171478: HP:0002818 Abnormality of the radius
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier II Human 25 Genes GS242172: [MeSH] 46, XX Disorders of Sex Development : D058489
Expand Human 360 Genes GS219927: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human 75 Genes GS176150: HP:0003019 Abnormality of the wrist
Expand Tier I Human 48 Genes GS176729: HP:0003042 Elbow dislocation
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human GO 140 Genes GS196530: GO:0000976 transcription regulatory region sequence-specific DNA binding
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Human 3385 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier II Human 2834 Genes GS245072: [MeSH] Pseudogenes : D011544
Expand Tier II Human 3394 Genes GS244643: [MeSH] Receptor Protein-Tyrosine Kinases : D020794
Expand Tier II Human 13694 Genes GS241851: [MeSH] Receptors, Cell Surface : D011956
Expand Tier I Human 93 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones
Expand Tier I Human GO 676 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Human 9 Genes GS171876: HP:0002990 Fibular aplasia
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 II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 24 Genes GS171104: HP:0006495 Aplasia/Hypoplasia of the ulna
Expand Tier I Human 142 Genes GS227483: MSigDB Geneset - KRAS.LUNG.BREAST_UP.V1_UP
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier II Human 316 Genes GS238792: [MeSH] Hindlimb : D006614
Expand Tier II Human 1835 Genes GS239653: [MeSH] Social Sciences : D012942
Expand Human 1470 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier II Human 184 Genes GS235153: [MeSH] Epiphyses : D004838
Expand Tier II Human 9876 Genes GS239522: [MeSH] Growth : D006128
Expand Tier II Human 607 Genes GS236328: [MeSH] Translocation, Genetic : D014178
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 30 Genes GS176012: HP:0003045 Abnormality of the patella
Expand Tier II Human 42 Genes GS234577: [MeSH] Hand : D006225
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 4977 Genes GS239472: [MeSH] Homeodomain Proteins : D018398
Expand Tier II Human 3644 Genes GS244377: [MeSH] Gonads : D006066
Expand Tier II Human 8647 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 58023 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier II Human 1266 Genes GS235704: [MeSH] Gonadal Disorders : D006058
Expand Tier II Human 785 Genes GS234966: [MeSH] Bone Development : D001846
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier II Human 70 Genes GS242447: [MeSH] Vagina : D014621
Expand Human 360 Genes GS219710: http://www.broadinstitute.org/gsea/msigdb/cards/EXTRACELLULAR_REGION_PART
Expand Tier I Human 123 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier II Human 3918 Genes GS237163: [MeSH] Peptide Hormones : D036361
Expand Tier I Human 208 Genes GS175164: HP:0011927 Short digit
Expand Human 63 Genes GS219618: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_VIRAL_MYOCARDITIS
Expand Tier II Human 6617 Genes GS235747: [MeSH] Musculoskeletal and Neural Physiological Phenomena : D055687
Expand Tier I Human 1 Genes GS173472: HP:0006436 Shortening of the tibia
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Human 1733 Genes GS219955: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier II Human 1026 Genes GS246010: [MeSH] Codon : D003062
Expand Tier I Human 16 Genes GS175109: HP:0003956 Bowed forearm bones
Expand Tier II Human 19354 Genes GS242551: [MeSH] Physiological Processes : D055705