Gene Details



SHOX and homologs in 4 species are found in 510 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 2067 Genes GS242641: [MeSH] Genes, Reporter : D017930
Expand Tier I Human 386 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human CTD 2637 Genes GS122408: vorinostat interacting with Homo sapiens associated genes (MeSH:C111237) in CTD
Expand Tier I Human 130 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier II Human 6197 Genes GS238238: [MeSH] Organelles : D015388
Expand Tier II Human 9028 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier II Human 468 Genes GS244888: [MeSH] Heart Defects, Congenital : D006330
Expand Tier II Human 1038 Genes GS242659: [MeSH] Islands : D062312
Expand Tier II Human 3028 Genes GS238474: [MeSH] Hormones : D006728
Expand Tier II Human 3671 Genes GS238182: [MeSH] Oncogene Proteins : D015513
Expand Tier I Human 15 Genes GS171103: HP:0006492 Aplasia/Hypoplasia of the fibula
Expand Tier II Human 1196 Genes GS242599: [MeSH] Enhancer Elements, Genetic : D004742
Expand Tier I Human 34 Genes GS172194: HP:0002970 Genu varum
Expand Tier I Human GO 7611 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier II Human 696 Genes GS243051: [MeSH] Adnexa Uteri : D000290
Expand Tier I Human GO 5182 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier II Human 3139 Genes GS241841: [MeSH] Genitalia : D005835
Expand Tier II Human 1331 Genes GS243677: [MeSH] Germ Layers : D005855
Expand Tier II Human 4818 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 415 Genes GS243964: [MeSH] Chromosome Deletion : D002872
Expand Tier I Human 281 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier II Human 1063 Genes GS245086: [MeSH] Skeleton : D012863
Expand Tier II Human 5070 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Human 202 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier II Human 548 Genes GS243263: [MeSH] Genes, Homeobox : D005801
Expand Tier I Human 551 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier II Human 635 Genes GS238428: [MeSH] Allelic Imbalance : D022981
Expand Tier I Human CTD 4420 Genes GS124185: Plant Extracts interacting with Homo sapiens associated genes (MeSH:D010936) in CTD
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 642 Genes GS172294: HP:0001510 Growth delay
Expand Tier II Human 7908 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier I Human 1 Genes GS176448: HP:0006459 Dorsal subluxation of ulna
Expand Tier I Human 124 Genes GS175665: HP:0006504 Abnormality involving the diaphyses of the limbs
Expand Tier I Human GO 12490 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 1003 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier II Human 489 Genes GS238289: [MeSH] Cardiovascular Abnormalities : D018376
Expand Tier II Human 5776 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Human 149 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier II Human 1743 Genes GS243816: [MeSH] Organogenesis : D038081
Expand Tier II Human 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human 41 Genes GS173378: HP:0002758 Osteoarthritis
Expand Tier I Human GO 5359 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier II Human 2992 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Human 31 Genes GS171877: HP:0002991 Abnormality of the fibula
Expand Tier II Human 49 Genes GS240888: [MeSH] X Chromosome Inactivation : D049951
Expand Tier II Human 101 Genes GS236323: [MeSH] Receptor, Fibroblast Growth Factor, Type 3 : D051498
Expand Tier II Human 9308 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier I Human 43 Genes GS176332: HP:0008873 Disproportionate short-limb short stature
Expand Tier II Human 1827 Genes GS236066: [MeSH] Musculoskeletal Physiological Phenomena : D009142
Expand Tier II Human 5524 Genes GS245439: [MeSH] Protein Kinases : D011494
Expand Tier I Human GO 9416 Genes GS196943: GO:0008152 metabolic process
Expand Tier II Human 781 Genes GS242013: [MeSH] Gene Duplication : D020440
Expand Tier I Human 134 Genes GS227140: MSigDB Geneset - chrxp22
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human GO 4064 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 130 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 358 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 937 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14517 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 750 Genes GS245677: [MeSH] X Chromosome : D014960
Expand Tier II Human 803 Genes GS238558: [MeSH] Tandem Repeat Sequences : D020080
Expand Tier I Human GO 4016 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 14551 Genes GS199634: GO:0005623 cell
Expand Tier II Human 725 Genes GS240024: [MeSH] Gene Dosage : D018628
Expand Tier II Human 338 Genes GS237845: [MeSH] Bone Diseases, Developmental : D001848
Expand Tier I Human 783 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier II Human 2524 Genes GS234776: [MeSH] Endocrine System : D004703
Expand Tier I Human 637 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 30 Genes GS176474: HP:0009821 Hypoplasia involving forearm bones
Expand Tier II Human 1544 Genes GS237303: [MeSH] Mutation, Missense : D020125
Expand Tier II Human 217 Genes GS240932: [MeSH] Chromosomes, Human, X : D041321
Expand Tier I Human 244 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier II Human 11234 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Human 488 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 211 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier II Human 73 Genes GS244530: [MeSH] Upper Extremity : D034941
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier II Human 935 Genes GS236780: [MeSH] Musculoskeletal Development : D041641
Expand Tier II Human 1970 Genes GS238775: [MeSH] Animal Structures : D000825
Expand Tier II Human 156 Genes GS240858: [MeSH] Urogenital Abnormalities : D014564
Expand Tier I Human GO 7309 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human 1099 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 1476 Genes GS241321: [MeSH] Untranslated Regions : D020506
Expand Tier I Human GO 8951 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier II Human 9373 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier II Human 676 Genes GS241290: [MeSH] Ovary : D010053
Expand Tier I Human CTD 422 Genes GS127198: Carmustine interacting with Homo sapiens associated genes (MeSH:D002330) in CTD
Expand Tier II Human 2386 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier I Human 118 Genes GS174314: HP:0002973 Abnormality of the forearm
Expand Tier II Human 3757 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier II Human 368 Genes GS236659: [MeSH] Codon, Terminator : D018388
Expand Tier I Human 52 Genes GS171286: HP:0002996 Limited elbow movement
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Human 5 Genes GS240491: [MeSH] Arm : D001132
Expand Tier I Human 951 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier II Human 1770 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Human 35 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier II Human 2446 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Human GO 4137 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12166 Genes GS201251: GO:0044424 intracellular part
Expand Tier II Human 3187 Genes GS239559: [MeSH] Oxidoreductases : D010088
Expand Tier I Human 19 Genes GS172642: HP:0002982 Tibial bowing
Expand Tier I Human GO 3892 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier II Human 10244 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Human 14 Genes GS176201: HP:0100777 Exostoses
Expand Tier I Human 49 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human GO 9519 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 514 Genes GS237532: [MeSH] Extremities : D005121
Expand Tier II Human 7063 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier II Human 3681 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier II Human 4598 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier II Human 2497 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 188 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier II Human 631 Genes GS241459: [MeSH] Psychology, Social : D011593
Expand Tier I Human 698 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 2225 Genes GS245543: [MeSH] Receptors, Peptide : D018000
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier II Human 6064 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier I Human 1 Genes GS175145: HP:0100745 Abnormality of the humeroulnar joint
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 3527 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier I Human 20 Genes GS175698: HP:0003022 Hypoplasia of the ulna
Expand Tier I Human 10 Genes GS173531: HP:0005772 Aplasia/Hypoplasia of the tibia
Expand Tier II Human 9588 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier II Human 120 Genes GS239107: [MeSH] Dwarfism : D004392
Expand Tier I Human 526 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Human 18573 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier II Human 1189 Genes GS235901: [MeSH] Mesoderm : D008648
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 892 Genes GS243817: [MeSH] Abnormalities, Multiple : D000015
Expand Tier II Human 2420 Genes GS242661: [MeSH] Endocrine System Diseases : D004700
Expand Tier I Human GO 5595 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier II Human 2479 Genes GS244436: [MeSH] Gene Frequency : D005787
Expand Tier I Human GO 5925 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 50 Genes GS172266: HP:0001191 Abnormality of the carpal bones
Expand Tier I Human 43 Genes GS171878: HP:0002992 Abnormality of the tibia
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 13572 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 3512 Genes GS234738: [MeSH] Proto-Oncogene Proteins : D011518
Expand Tier I Human 734 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 17884 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 3551 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human 5 Genes GS175975: HP:0010044 Short 4th metacarpal
Expand Tier I Human 63 Genes GS175660: HP:0006501 Aplasia/Hypoplasia of the radius
Expand Tier II Human 192 Genes GS234778: [MeSH] Growth Disorders : D006130
Expand Tier I Human 194 Genes GS228625: MSigDB Geneset - GSE9006_HEALTHY_VS_TYPE_2_DIABETES_PBMC_AT_DX_DN
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human 53 Genes GS172644: HP:0002981 Abnormality of the calf
Expand Tier II Human 604 Genes GS243339: [MeSH] Musculoskeletal Abnormalities : D009139
Expand Tier II Human 76 Genes GS238794: [MeSH] Sexual and Gender Disorders : D019968
Expand Tier II Human 2729 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Human 83 Genes GS172024: HP:0001369 Arthritis
Expand Tier I Human 10 Genes GS173229: HP:0005736 Hypoplastic tibia
Expand Tier I Human 9 Genes GS172493: HP:0003038 Fibular hypoplasia
Expand Tier II Human 523 Genes GS243243: [MeSH] Pituitary Hormones, Anterior : D010908
Expand Tier II Human 2507 Genes GS235830: [MeSH] Cardiovascular Diseases : D002318
Expand Tier I Human 393 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 347 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier II Human 587 Genes GS242703: [MeSH] Ploidies : D011003
Expand Tier II Human 3976 Genes GS239550: [MeSH] Apoptosis : D017209
Expand Tier II Human 173 Genes GS235191: [MeSH] Y Chromosome : D014998
Expand Tier I Human 78 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier II Human 1875 Genes GS245892: [MeSH] Musculoskeletal Diseases : D009140
Expand Tier II Human 17815 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 802 Genes GS243625: [MeSH] Sex Chromosomes : D012730
Expand Tier I Human GO 1002 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human 318 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 396 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier II Human 13 Genes GS243006: [MeSH] Sex Chromosome Disorders of Sex Development : D058533
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier II Human 1984 Genes GS237733: [MeSH] Mental Disorders : D001523
Expand Tier I Human 41 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier II Human 2174 Genes GS238322: [MeSH] Behavior and Behavior Mechanisms : D001520
Expand Tier I Human 488 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 6916 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier II Human 10126 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human CTD 2637 Genes GS253624: repinotan hydrochloride interacting with nan associated genes (MeSH:C111221) in CTD
Expand Tier II Human 48 Genes GS235059: [MeSH] Sex Chromosome Disorders : D025064
Expand Tier II Human 1704 Genes GS241605: [MeSH] Embryo, Nonmammalian : D004625
Expand Tier II Human 5682 Genes GS242677: [MeSH] Phosphotransferases (Alcohol Group Acceptor) : D017853
Expand Tier II Human 713 Genes GS238378: [MeSH] Chick Embryo : D002642
Expand Tier II Human 4398 Genes GS238280: [MeSH] Cell Cycle : D002453
Expand Tier II Human 897 Genes GS235231: [MeSH] Bone and Bones : D001842
Expand Tier II Human 6287 Genes GS239526: [MeSH] Phosphotransferases : D010770
Expand Tier I Human 599 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human GO 4552 Genes GS196806: GO:0032502 developmental process
Expand Tier II Human 3665 Genes GS239266: [MeSH] Morphogenesis : D009024
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 2419 Genes GS244537: [MeSH] Protein-Tyrosine Kinases : D011505
Expand Tier I Human 28 Genes GS176426: HP:0003063 Abnormality of the humerus
Expand Tier I Human 804 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier II Human 1141 Genes GS236278: [MeSH] Chromosome Aberrations : D002869
Expand Tier II Human 7052 Genes GS243346: [MeSH] Chromosomes, Human : D002877
Expand Tier I Human GO 1390 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human GO 10580 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 279 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier II Human 152 Genes GS243862: [MeSH] Osteochondrodysplasias : D010009
Expand Tier II Human 622 Genes GS238897: [MeSH] Sociology : D012961
Expand Tier II Human 6649 Genes GS238537: [MeSH] Pharmacological Phenomena : D002620
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier II Human 18638 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Human GO 4683 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 385 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human 29 Genes GS173982: HP:0001454 Abnormality of the upper arm
Expand Tier I Human 402 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier II Human 11248 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier II Human 6703 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier I Human 1204 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier II Human 15234 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Human GO 2313 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human 555 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier II Human 7665 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier II Human 65 Genes GS236296: [MeSH] Haploinsufficiency : D057895
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier II Human 812 Genes GS238243: [MeSH] Bone Diseases : D001847
Expand Tier II Human 2529 Genes GS241608: [MeSH] Haplotypes : D006239
Expand Tier II Human 637 Genes GS236202: [MeSH] Microsatellite Repeats : D018895
Expand Tier II Human 2944 Genes GS236700: [MeSH] Musculoskeletal System : D009141
Expand Tier II Human 246 Genes GS236399: [MeSH] Consanguinity : D003241
Expand Tier I Human GO 5627 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 332 Genes GS196532: GO:0000975 regulatory region DNA binding
Expand Tier II Human 7529 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Human GO 9530 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 21 Genes GS172117: HP:0002984 Hypoplasia of the radius
Expand Tier I Human 5 Genes GS174277: HP:0010042 Aplasia/Hypoplasia of the 4th metacarpal
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier II Human 11267 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Tier II Human 7336 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier II Human 386 Genes GS235824: [MeSH] 5' Untranslated Regions : D020121
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Human 28 Genes GS234900: [MeSH] Sex Chromosome Aberrations : D012729
Expand Tier I Human GO 9158 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 17816 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier I Human 124 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier II Human 7732 Genes GS243763: [MeSH] Intracellular Space : D042541
Expand Tier II Human 11302 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier I Human 577 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier II Human 4197 Genes GS235286: [MeSH] Cell Death : D016923
Expand Tier II Human 3740 Genes GS240223: [MeSH] Down-Regulation : D015536
Expand Tier II Human 220 Genes GS245370: [MeSH] Limb Deformities, Congenital : D017880
Expand Tier I Human 94 Genes GS174308: HP:0002979 Bowing of the legs
Expand Tier I Human GO 15161 Genes GS194087: GO:0003674 molecular_function
Expand Tier II Human 4260 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human 597 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier II Human 1968 Genes GS241690: [MeSH] Female Urogenital Diseases : D052776
Expand Tier II Human 1883 Genes GS244414: [MeSH] Arthropod Proteins : D060829
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier II Human 27 Genes GS239099: [MeSH] Mullerian Ducts : D009095
Expand Tier II Human 3038 Genes GS241307: [MeSH] Hormones, Hormone Substitutes, and Hormone Antagonists : D006730
Expand Tier II Human 134 Genes GS238765: [MeSH] Dosage Compensation, Genetic : D004303
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier I Human GO 10565 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier II Human 18556 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Human GO 5411 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier II Human 1245 Genes GS235642: [MeSH] Body Regions : D001829
Expand Tier II Human 2265 Genes GS244384: [MeSH] Female Urogenital Diseases and Pregnancy Complications : D005261
Expand Tier II Human 83 Genes GS237462: [MeSH] Genomic Structural Variation : D056914
Expand Tier II Human 7025 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Human 263 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 54 Genes GS171298: HP:0002829 Arthralgia
Expand Tier II Human 3643 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier I Human 396 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 7440 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Human 2 Genes GS174079: HP:0002762 Multiple exostoses
Expand Tier I Human 21 Genes GS175859: HP:0006443 Patellar aplasia
Expand Tier I Human 11 Genes GS172115: HP:0002986 Radial bowing
Expand Tier II Human 10 Genes GS241894: [MeSH] Turner Syndrome : D014424
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier I Human 45 Genes GS175084: HP:0008384 Aplastic/hypoplastic fingernail
Expand Tier II Human 114 Genes GS242840: [MeSH] Disorders of Sex Development : D012734
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 5 Genes GS172291: HP:0003067 Madelung deformity
Expand Tier II Human 15970 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human GO 5911 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 179 Genes GS230055: MSigDB Geneset - GSE17974_0H_VS_1H_IN_VITRO_ACT_CD4_TCELL_UP
Expand Tier II Human 2806 Genes GS237404: [MeSH] Chromosomes, Human, 6-12 and X : D002906
Expand Tier II Human 1878 Genes GS245484: [MeSH] Insect Proteins : D019476
Expand Tier II Human 3351 Genes GS244779: [MeSH] Embryonic and Fetal Development : D005314
Expand Tier II Human 394 Genes GS244425: [MeSH] Receptors, Fibroblast Growth Factor : D017468
Expand Tier I Human 2330 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Human 13379 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier II Human 443 Genes GS240790: [MeSH] Chondrocytes : D019902
Expand Tier I Human 445 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human 281 Genes GS172572: HP:0000347 Micrognathia
Expand Tier II Human 4608 Genes GS243806: [MeSH] Time : D013995
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 79 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier II Human 152 Genes GS235576: [MeSH] Growth Plate : D006132
Expand Tier I Human 58 Genes GS171822: HP:0000112 Nephropathy
Expand Tier II Human 83 Genes GS244957: [MeSH] DNA Copy Number Variations : D056915
Expand Tier I Human GO 324 Genes GS202371: GO:0044212 transcription regulatory region DNA binding
Expand Tier I Human GO 1000 Genes GS195678: GO:0003700 sequence-specific DNA binding transcription factor activity
Expand Tier II Human 26 Genes GS237629: [MeSH] Gonadal Dysgenesis : D006059
Expand Tier II Human 7493 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier I Human 148 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier II Human 7446 Genes GS239443: [MeSH] RNA Splicing : D012326
Expand Tier I Human 336 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier II Human 4230 Genes GS234532: [MeSH] Sequence Deletion : D017384
Expand Tier I Human GO 332 Genes GS208604: GO:0001067 regulatory region nucleic acid binding
Expand Tier II Human 9339 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier II Human 9390 Genes GS235446: [MeSH] Reproductive and Urinary Physiological Phenomena : D012101
Expand Tier II Human 11557 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier I Human 262 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier II Human 7 Genes GS239239: [MeSH] Luciferases, Firefly : D049409
Expand Tier II Human 1096 Genes GS234046: [MeSH] Genitalia, Female : D005836
Expand Tier II Human 588 Genes GS239408: [MeSH] Pituitary Hormones : D010907
Expand Tier II Human 483 Genes GS237355: [MeSH] Aneuploidy : D000782
Expand Tier I Human 195 Genes GS230270: MSigDB Geneset - GSE360_CTRL_VS_B_MALAYI_LOW_DOSE_MAC_DN
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 424 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 1069 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier II Human 10111 Genes GS235272: [MeSH] Membrane Proteins : D008565
Expand Tier II Human 644 Genes GS240209: [MeSH] Uterus : D014599
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 97 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier II Human 47 Genes GS240183: [MeSH] Chromosomes, Human, Y : D041322
Expand Tier I Human 8 Genes GS175564: HP:0003027 Mesomelia
Expand Tier II Human 6093 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Human CTD 188 Genes GS121485: deoxynivalenol interacting with Sus scrofa associated genes (MeSH:C007262) in CTD
Expand Tier I Human 185 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier II Human 160 Genes GS239950: [MeSH] Growth Hormone : D013006
Expand Tier II Human 62 Genes GS233995: [MeSH] Human Growth Hormone : D019382
Expand Tier I Human 32 Genes GS172698: HP:0002653 Bone pain
Expand Tier II Human 1154 Genes GS243764: [MeSH] Connective Tissue : D003238
Expand Tier II Human 7335 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier II Human 14403 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 55 Genes GS176473: HP:0003498 Disproportionate short stature
Expand Tier II Human 34 Genes GS241822: [MeSH] Haploidy : D006238
Expand Tier I Human 777 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 434 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 781 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier II Human 6299 Genes GS242721: [MeSH] Physical Phenomena : D055585
Expand Tier I Human GO 12781 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 139 Genes GS174847: HP:0000940 Abnormal diaphysis morphology
Expand Tier I Human GO 3179 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 67 Genes GS172110: HP:0002983 Micromelia
Expand Tier II Human 1250 Genes GS242635: [MeSH] Luciferases : D008156
Expand Tier II Human 4760 Genes GS239365: [MeSH] Pharmacological Processes : D055632
Expand Tier I Human GO 6609 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 84 Genes GS172316: HP:0003026 Short long bones
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 12777 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 7201 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier II Human 633 Genes GS241012: [MeSH] Loss of Heterozygosity : D019656
Expand Tier I Human GO 8546 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5345 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier II Human 416 Genes GS245028: [MeSH] Monosomy : D009006
Expand Tier II Human 11159 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 3507 Genes GS193991: GO:0048731 system development
Expand Tier II Human 1669 Genes GS237394: [MeSH] Point Mutation : D017354
Expand Tier I Human GO 3604 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human 301 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 5565 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier II Human 8835 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier I Human 61 Genes GS174139: HP:0005914 Aplasia/Hypoplasia involving the metacarpal bones
Expand Tier I Human 357 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human 38 Genes GS172268: HP:0001193 Ulnar deviation of the hand or of fingers of the hand
Expand Tier I Human 122 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human GO 11880 Genes GS198263: GO:0005488 binding
Expand Tier II Human 675 Genes GS237234: [MeSH] Chromosomes, Human, 21-22 and Y : D002904
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Human 239 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human GO 5524 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3282 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier II Human 11230 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 7110 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier II Human 737 Genes GS245745: [MeSH] Chromosome Disorders : D025063
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 Human 2 Genes GS173924: HP:0004986 Rudimentary to absent fibulae
Expand Tier I Human 117 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier II Human 1747 Genes GS234306: [MeSH] Receptors, Growth Factor : D017978
Expand Tier II Human 1628 Genes GS246018: [MeSH] Heart Diseases : D006331
Expand Tier II Human 7556 Genes GS245348: [MeSH] RNA Processing, Post-Transcriptional : D012323
Expand Tier II Human 661 Genes GS238687: [MeSH] Disease : D004194
Expand Tier II Human 6986 Genes GS237339: [MeSH] Regulatory Sequences, Nucleic Acid : D012045
Expand Tier I Human 272 Genes GS229012: MSigDB Geneset - KRAS.600.LUNG.BREAST_UP.V1_UP
Expand Tier II Human 340 Genes GS239233: [MeSH] Codon, Nonsense : D018389
Expand Tier I Human CTD 422 Genes GS251766: Carmine interacting with nan associated genes (MeSH:D002329) in CTD
Expand Tier I Human GO 3265 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier II Human 646 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Human 85 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Human 47 Genes GS174089: HP:0003367 Abnormality of the femoral neck
Expand Tier II Human 6676 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 111 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 575 Genes GS243813: [MeSH] Family : D005190
Expand Tier II Human 5312 Genes GS237745: [MeSH] Epigenesis, Genetic : D044127
Expand Tier II Human 6493 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier II Human 1722 Genes GS245998: [MeSH] Musculoskeletal Physiological Processes : D043702
Expand Tier I Human 54 Genes GS172140: HP:0002857 Genu valgum
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 15 Genes GS172482: HP:0003032 Short femoral neck
Expand Tier I Human 395 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7265 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier II Human 4933 Genes GS245206: [MeSH] Cell Nucleus : D002467
Expand Tier I Human 187 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 10961 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier II Human 1346 Genes GS245900: [MeSH] Fetus : D005333
Expand Tier I Human GO 3618 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 103 Genes GS171478: HP:0002818 Abnormality of the radius
Expand Tier II Human 24 Genes GS242172: [MeSH] 46, XX Disorders of Sex Development : D058489
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 76 Genes GS176150: HP:0003019 Abnormality of the wrist
Expand Tier I Human GO 140 Genes GS196530: GO:0000976 transcription regulatory region sequence-specific DNA binding
Expand Tier I Human GO 3698 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human 48 Genes GS176729: HP:0003042 Elbow dislocation
Expand Tier II Human 8777 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier II Human 862 Genes GS245072: [MeSH] Pseudogenes : D011544
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier II Human 1643 Genes GS244643: [MeSH] Receptor Protein-Tyrosine Kinases : D020794
Expand Tier II Human 5184 Genes GS241851: [MeSH] Receptors, Cell Surface : D011956
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 71 Genes GS175658: HP:0006503 Aplasia/Hypoplasia involving forearm bones
Expand Tier I Human GO 675 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Human GO 8649 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 9 Genes GS171876: HP:0002990 Fibular aplasia
Expand Tier I Human 986 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier II Human 18365 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 GO 4244 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier II Human 1577 Genes GS239653: [MeSH] Social Sciences : D012942
Expand Tier II Human 258 Genes GS238792: [MeSH] Hindlimb : D006614
Expand Tier I Human 137 Genes GS227483: MSigDB Geneset - KRAS.LUNG.BREAST_UP.V1_UP
Expand Tier I Human GO 14550 Genes GS208012: GO:0044464 cell part
Expand Tier II Human 153 Genes GS235153: [MeSH] Epiphyses : D004838
Expand Tier II Human 4823 Genes GS239522: [MeSH] Growth : D006128
Expand Tier II Human 461 Genes GS236328: [MeSH] Translocation, Genetic : D014178
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 30 Genes GS176012: HP:0003045 Abnormality of the patella
Expand Tier I Human GO 5335 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 515 Genes GS174081: HP:0004322 Short stature
Expand Tier II Human 39 Genes GS234577: [MeSH] Hand : D006225
Expand Tier II Human 2419 Genes GS239472: [MeSH] Homeodomain Proteins : D018398
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 1824 Genes GS244377: [MeSH] Gonads : D006066
Expand Tier II Human 5214 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier I Human 565 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier II Human 974 Genes GS235704: [MeSH] Gonadal Disorders : D006058
Expand Tier I Human 287 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier II Human 567 Genes GS234966: [MeSH] Bone Development : D001846
Expand Tier II Human 57 Genes GS242447: [MeSH] Vagina : D014621
Expand Tier I Human 124 Genes GS170894: HP:0006487 Bowing of the long bones
Expand Tier II Human 1952 Genes GS237163: [MeSH] Peptide Hormones : D036361
Expand Tier I Human 209 Genes GS175164: HP:0011927 Short digit
Expand Tier II Human 2582 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 11279 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Human GO 3715 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process