Gene Details



ADAMTS10 and homologs in 7 species are found in 454 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 I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 386 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier II Human 9028 Genes GS241666: [MeSH] Sequence Homology, Amino Acid : D017386
Expand Tier II Human 8283 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Human 878 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier II Mouse 945 Genes GS136704: systemic lupus erythmatosus suppressor 1 (Sles1, Published QTL Chr 17)
Expand Tier I Human 187 Genes GS228983: MSigDB Geneset - GSE14000_UNSTIM_VS_4H_LPS_DC_TRANSLATED_RNA_DN
Expand Tier II Human 9751 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Human 1177 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Mouse 948 Genes GS135590: P. chabaudi malaria resistance QTL 3 (Char3, Published QTL Chr 17)
Expand Tier II Mouse 947 Genes GS136392: organ weight 10 (Org10, Published QTL Chr 17)
Expand Tier I Mouse GO 171 Genes GS182225: GO:0008237 metallopeptidase activity
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier II Mouse 947 Genes GS136833: trypanosome infection response 1 (Tir1, Published QTL Chr 17)
Expand Tier II Mouse 948 Genes GS135229: Angiostrongylus costaricensis nematode susceptibility 3 (Acsns3, Published QTL Chr 17)
Expand Tier I Mouse GO 3536 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 642 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 319 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier II Human 17829 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 14843 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Mouse GO 22753 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Mouse 714 Genes GS135641: circadian photosensitivity 2 (Circp2, Published QTL Chr 17)
Expand Tier II Human 2992 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse 194 Genes GS229875: MSigDB Geneset - GSE31082_DN_VS_CD8_SP_THYMOCYTE_DN
Expand Tier II Human 9308 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier II Human 4853 Genes GS239764: [MeSH] Glycoproteins : D006023
Expand Tier I Human 376 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 17829 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human 490 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 358 Genes GS172701: HP:0002650 Scoliosis
Expand Tier II Mouse 862 Genes GS136305: modifier of Yaa 2 (Myaa2, Published QTL Chr 17)
Expand Tier I Human 15 Genes GS173460: HP:0001653 Mitral regurgitation
Expand Tier I Human 148 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1207 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 31 Genes GS172056: HP:0001500 Broad finger
Expand Tier II Human 338 Genes GS237845: [MeSH] Bone Diseases, Developmental : D001848
Expand Tier I Human 168 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 11 Genes GS175392: HP:0011003 Severe Myopia
Expand Tier I Human 531 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 783 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 637 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier II Mouse 943 Genes GS136509: particle-induced immune disfunction (Pidys, Published QTL Chr 17)
Expand Tier II Human 11234 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Rat DRG 4708 Genes GS86494: Table S1: Hippocampus 17 K microarray data. [DRG]
Expand Tier I Human 782 Genes GS229049: MSigDB Geneset - TAATTA_V$CHX10_01
Expand Tier I Human 488 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Mouse 195 Genes GS229603: MSigDB Geneset - GSE17721_0.5H_VS_12H_GARDIQUIMOD_BMDM_UP
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier II Human 4996 Genes GS236915: [MeSH] Genome, Human : D015894
Expand Tier I Human GO 8951 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human CTD 1896 Genes GS123981: propionaldehyde interacting with Homo sapiens associated genes (MeSH:C005556) in CTD
Expand Tier II Rat 777 Genes GS224456: White blood cell count QTL 4 (Wbc4 Published QTL Chr 7)
Expand Tier I Human CTD 2708 Genes GS124165: Hydrogen Peroxide interacting with Homo sapiens associated genes (MeSH:D006861) in CTD
Expand Tier II Human 14808 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human CTD 758 Genes GS126989: Hydralazine interacting with Homo sapiens associated genes (MeSH:D006830) in CTD
Expand Tier I Human 20 Genes GS171556: HP:0001387 Joint stiffness
Expand Tier I Mouse GO 3548 Genes GS184566: GO:0019538 protein metabolic process
Expand Tier I Human GO 178 Genes GS199022: GO:0008237 metallopeptidase activity
Expand Tier I Human 1219 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 600 Genes GS182209: GO:0008233 peptidase activity
Expand Tier I Mouse GO 98 Genes GS183020: GO:0004222 metalloendopeptidase activity
Expand Tier II Rat 587 Genes GS224849: Neuroinflammation QTL 5 (Neuinf5 Published QTL Chr 7)
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Human 887 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier II Human 1770 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Human 951 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 35 Genes GS173309: HP:0002938 Lumbar hyperlordosis
Expand Tier II Mouse 890 Genes GS136861: "T cell receptor beta variable 4, control 1" (Trbv4c1, Published QTL Chr 17)
Expand Tier II Human 667 Genes GS241590: [MeSH] Extracellular Matrix : D005109
Expand Tier I Human GO 575 Genes GS199006: GO:0008233 peptidase activity
Expand Tier II Human 10244 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Mouse GO 3441 Genes GS181533: GO:0046872 metal ion binding
Expand Tier II Human 5821 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier I Human 25 Genes GS174125: HP:0008063 Aplasia/Hypoplasia of the lens
Expand Tier I Human 188 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier II Mouse 593 Genes GS135576: cystic fibrosis lung disease 3 (Cfld3, Published QTL Chr 17)
Expand Tier II Mouse 915 Genes GS136226: mandible length 18 (Manln18, Published QTL Chr 17)
Expand Tier II Mouse 949 Genes GS136800: total body bone mineral density 7 (Tbbmd7, Published QTL Chr 17)
Expand Tier II Mouse 885 Genes GS136903: ventral midbrain iron content 9 (Vmbic9, Published QTL Chr 17)
Expand Tier II Mouse 890 Genes GS136157: leishmaniasis resistance 1 (Lmr1, Published QTL Chr 17)
Expand Tier I Human 30 Genes GS175042: HP:0009768 Broad phalanges of the hand
Expand Tier I Human GO 1093 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 708 Genes GS228167: MSigDB Geneset - TGTTTGY_V$HNF3_Q6
Expand Tier II Human 64 Genes GS235332: [MeSH] Disintegrins : D019483
Expand Tier I Human 1056 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier II Rat 730 Genes GS223259: Neuroinflammation QTL 6 (Neuinf6 Published QTL Chr 7)
Expand Tier I Human 188 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human 12 Genes GS172101: HP:0000586 Shallow orbits
Expand Tier II Human 6064 Genes GS237183: [MeSH] Growth and Development : D048788
Expand Tier II Human 7832 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 698 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 5 Genes GS175743: HP:0001230 Broad metacarpals
Expand Tier II Human 3527 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier II Human 14167 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 9588 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier II Mouse 945 Genes GS135462: bleomycin pulmonary fibrosis 1 (Bplpf1, Published QTL Chr 17)
Expand Tier II Human 120 Genes GS239107: [MeSH] Dwarfism : D004392
Expand Tier II Human 18573 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 526 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Mouse 947 Genes GS135227: anticardiolipin antibody 1 (Acla1, Published QTL Chr 17)
Expand Tier II Human 14336 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier II Human 1048 Genes GS240795: [MeSH] Eye Diseases : D005128
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 II Rat 669 Genes GS223722: Body weight QTL 19 (Bw19 Published QTL Chr 7)
Expand Tier I Human 543 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human CTD 758 Genes GS251594: Hydantoins interacting with Homo sapiens associated genes (MeSH:D006827) in CTD
Expand Tier II Mouse 915 Genes GS136400: organ weight 9 (Org9, Published QTL Chr 17)
Expand Tier II Human 15107 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier II Rat 1534 Genes GS224139: Anxiety related response QTL 17 (Anxrr17 Published QTL Chr 7)
Expand Tier I Human GO 1979 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier II Mouse 948 Genes GS135736: delta power in slow-wave sleep 3 (Dps3, Published QTL Chr 17)
Expand Tier II Human 17884 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Mouse CTD 979 Genes GS257004: Succimer interacting with Mus musculus associated genes (MeSH:D004113) in CTD
Expand Tier II Human 192 Genes GS234778: [MeSH] Growth Disorders : D006130
Expand Tier I Human GO 2222 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier II Mouse 948 Genes GS135924: hepatocarcinogenesis in females 1 (Hcif1, Published QTL Chr 17)
Expand Tier II Mouse 817 Genes GS83968: cocaine induced activation 13 (Cocia13, Published QTL, Chr 17)
Expand Tier I Human 206 Genes GS269340: GWAS Catalog Data for body height in 253,288 European ancestry individuals
Expand Tier I Human CTD 4614 Genes GS127240: Acetaminophen interacting with Homo sapiens associated genes (MeSH:D000082) in CTD
Expand Tier II Human 2729 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Mouse CTD 1018 Genes GS255823: Bleaching Agents interacting with Mus musculus associated genes (MeSH:D057886) in CTD
Expand Tier II Mouse 853 Genes GS84302: differences in cocaine responsiveness (Published QTL, Chr 17)
Expand Tier I Mouse GO 8412 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier II Mouse 76 Genes GS36163: Neocortex Gene expression correlates of Locomotor response of 10 mg/kg MDMA injected on Day 2 in Males BXD
Expand Tier II Human 1009 Genes GS238836: [MeSH] Metalloproteases : D045726
Expand Tier II Human 1875 Genes GS245892: [MeSH] Musculoskeletal Diseases : D009140
Expand Tier I Human 78 Genes GS172684: HP:0003307 Hyperlordosis
Expand Tier II Human 16597 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 17815 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier II Mouse 856 Genes GS135650: cocaine induced activation 13 (Cocia13, Published QTL Chr 17)
Expand Tier I Human 318 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier II Mouse 896 Genes GS84300: METH responses for body temperature (Published QTL, Chr 17)
Expand Tier I Mouse 193 Genes GS228960: MSigDB Geneset - GSE17721_PAM3CSK4_VS_CPG_8H_BMDM_UP
Expand Tier I Human 396 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier II Mouse 885 Genes GS136887: UVB induced immunosuppression 2 (Uvbi2, Published QTL Chr 17)
Expand Tier II Human 16030 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Human 8 Genes GS176246: HP:0001783 Broad metatarsal
Expand Tier I Human 27 Genes GS173688: HP:0001642 Pulmonic stenosis
Expand Tier I Human GO 4009 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 488 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 30 Genes GS172669: HP:0003103 Abnormal cortical bone morphology
Expand Tier II Mouse 947 Genes GS135324: antibody response to human factor IX (Arfix, Published QTL Chr 17)
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier II Human 17816 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Human 1500 Genes GS231868: PC Geneset - "Metabolism of proteins" pathway genes
Expand Tier II Human 10126 Genes GS237194: [MeSH] Physiological Phenomena : D010829
Expand Tier I Human 1163 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Mouse 915 Genes GS135556: CD8 memory T cell subset 5 (Cd8mts5, Published QTL Chr 17)
Expand Tier II Mouse 902 Genes GS135763: experimental allergic encephalomyelitis susceptibility 5 (Eae5, Published QTL Chr 17)
Expand Tier I Human 599 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 774 Genes GS231670: PC Geneset - "TAATTA_V$CHX10_01" pathway genes
Expand Tier II Human 11962 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Mouse 198 Genes GS228929: MSigDB Geneset - GSE17721_CTRL_VS_GARDIQUIMOD_12H_BMDM_UP
Expand Tier I Human 804 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 2107 Genes GS210214: GO:0005576 extracellular region
Expand Tier II Human 18212 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Mouse 856 Genes GS135256: adenovirus induced hyperthyroidism 2 (Advh2, Published QTL Chr 17)
Expand Tier II Mouse 945 Genes GS136083: keratoconus 1 (Krcn1, Published QTL Chr 17)
Expand Tier II Human 11733 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Human GO 8 Genes GS209921: GO:0001527 microfibril
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier II Human 18638 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Human 244 Genes GS268572: GWAS Catalog Data for body height in 133,653 European ancestry individuals
Expand Tier II Rat 744 Genes GS224336: Body weight QTL 136 (Bw136 Published QTL Chr 7)
Expand Tier I Human 402 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier II Mouse 643 Genes GS135687: CD86 expression in activated macrophages (Cxam, Published QTL Chr 17)
Expand Tier II Human 11248 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
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 II Mouse 949 Genes GS136120: body length 9 (Lgth9, Published QTL Chr 17)
Expand Tier I Human GO 3868 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 156 Genes GS267954: GWAS Catalog Data for body height in 30,968 European ancestry individuals
Expand Tier II Human 16814 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 7665 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Human 555 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier II Human 812 Genes GS238243: [MeSH] Bone Diseases : D001847
Expand Tier I Rat CTD 13841 Genes GS267227: bisphenol A interacting with Rattus norvegicus associated genes (MeSH:C006780) in CTD
Expand Tier II Mouse 949 Genes GS135861: femur breaking strength 4 (Fembrs4, Published QTL Chr 17)
Expand Tier II Mouse 656 Genes GS136483: plasmacytoma susceptibility 5 (Pcyts5, Published QTL Chr 17)
Expand Tier II Mouse 948 Genes GS136773: SGC/Knj cross B6 QTL 3 (Sxbq3, Published QTL Chr 17)
Expand Tier I Human 32 Genes GS171295: HP:0003508 Proportionate short stature
Expand Tier II Human 7529 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Human 43 Genes GS270968: GWAS Catalog Data for atopic eczema in 18,900 European ancestry cases, 1,472 Japanese ancestry cases, 422 African American cases, 300 Latino cases, 305 cases, 84,166 European ancestry controls, 7,966 Japanese ancestry controls, 844 African American controls, 1,592 Latino controls, 896 controls
Expand Tier II Mouse 947 Genes GS136092: long bones 10 (Lbn10, Published QTL Chr 17)
Expand Tier II Human 11267 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Tier I Mouse GO 862 Genes GS182673: GO:0006508 proteolysis
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier II Rat 568 Genes GS224186: Bone mineral density QTL 15 (Bmd15 Published QTL Chr 7)
Expand Tier II Human 19180 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human 199 Genes GS229352: MSigDB Geneset - V$RP58_01
Expand Tier I Human GO 9158 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier II Human 17816 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier I Mouse GO 1341 Genes GS186836: GO:0008270 zinc ion binding
Expand Tier II Human 17454 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 124 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier II Mouse 919 Genes GS135331: autoimmune susceptibility in C57BL/6J and BALB/c 3 (Asbb3, Published QTL Chr 17)
Expand Tier III Mouse 7750 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampus
Expand Tier II Human 11302 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier I Human 17 Genes GS173461: HP:0001650 Aortic valve stenosis
Expand Tier II Human 3632 Genes GS234929: [MeSH] Plasmids : D010957
Expand Tier II Human 950 Genes GS245958: [MeSH] Metalloendopeptidases : D008666
Expand Tier I Human 577 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human CTD 3490 Genes GS127166: bisphenol A interacting with Oryzias latipes associated genes (MeSH:C006780) in CTD
Expand Tier II Mouse 915 Genes GS135616: circulating hormone level QTL 8 (Chlq8, Published QTL Chr 17)
Expand Tier I Human 1489 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Mouse GO 11 Genes GS178053: GO:0043205 fibril
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15161 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 597 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human GO 360 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier II Mouse 1006 Genes GS84301: ethanol conditioned taste aversion (Published QTL, Chr 17)
Expand Tier I Human GO 185 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier II Human 10556 Genes GS235415: [MeSH] Embryo, Mammalian : D004622
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier I Mouse GO 22332 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Human 17923 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 16633 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Mouse 947 Genes GS136437: platelet-binding antibody-associated thrombocytopenia 1 (Pbat1, Published QTL Chr 17)
Expand Tier II Human 18556 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Mouse GO 5224 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 708 Genes GS232230: PC Geneset - "TGTTTGY_V$HNF3_Q6" pathway genes
Expand Tier II Mouse 924 Genes GS136265: modifier of mammary tumor progression 2 (Mmtp2, Published QTL Chr 17)
Expand Tier II Mouse 947 Genes GS136686: skull morphology 25 (Skull25, Published QTL Chr 17)
Expand Tier I Mouse GO 2188 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Human 18 Genes GS171852: HP:0000593 Abnormality of the anterior chamber
Expand Tier I Human 396 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human CTD 3575 Genes GS255189: Bisecurin I interacting with Homo sapiens associated genes (MeSH:C018467) in CTD
Expand Tier I Mouse CTD 7038 Genes GS255863: Nanotubes, Carbon interacting with Mus musculus associated genes (MeSH:D037742) in CTD
Expand Tier II Human 7440 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Mouse 949 Genes GS136479: periosteal circumference 4 (Pcir4, Published QTL Chr 17)
Expand Tier II Mouse 638 Genes GS135250: adiposity 18 (Adip18, Published QTL Chr 17)
Expand Tier I Human 12 Genes GS170954: HP:0000885 Broad ribs
Expand Tier II Human 10170 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 15712 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 9047 Genes GS180166: GO:0008152 metabolic process
Expand Tier II Rat 885 Genes GS224058: Pain QTL 2 (Pain2 Published QTL Chr 7)
Expand Tier II Mouse 593 Genes GS136482: plasmacytoma susceptibility 4 (Pcyts4, Published QTL Chr 17)
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Human 2330 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Mouse 915 Genes GS136909: vertebral morphology and mechanical traits 14 (Vmmt14, Published QTL Chr 17)
Expand Tier I Human 445 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5774 Genes GS206742: GO:0043167 ion binding
Expand Tier II Mouse 40 Genes GS36461: Neocortex Gene expression correlates of Morphine - Postural Effects in Males BXD
Expand Tier II Mouse 809 Genes GS136634: small effect CIA locus 8 (Secia8, Published QTL Chr 17)
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier II Human 13540 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier II Mouse 909 Genes GS135782: early growth QTL 5 (Egq5, Published QTL Chr 17)
Expand Tier I Human 7 Genes GS173383: HP:0002753 Thin bony cortex
Expand Tier II Human 15098 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier I Human GO 12 Genes GS194800: GO:0043205 fibril
Expand Tier II Mouse 656 Genes GS135592: P. chabaudi malaria resistance QTL 7 (Char7, Published QTL Chr 17)
Expand Tier I Human 148 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 336 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier II Human 5292 Genes GS239596: [MeSH] Expressed Sequence Tags : D020224
Expand Tier I Mouse 1098 Genes GS128599: Ethanol Induced Ataxia Chr#17
Expand Tier II Human 9339 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier II Human 2352 Genes GS241873: [MeSH] Glycoconjugates : D006001
Expand Tier I Human CTD 1467 Genes GS121243: 5-dihydrocortisone interacting with Homo sapiens associated genes (MeSH:C045993) in CTD
Expand Tier II Human 9390 Genes GS235446: [MeSH] Reproductive and Urinary Physiological Phenomena : D012101
Expand Tier I Human 362 Genes GS173991: HP:0000505 Visual impairment
Expand Tier II Human 11557 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier II Mouse 909 Genes GS136942: weight 10 weeks QTL 12 (W10q12, Published QTL Chr 17)
Expand Tier I Human 262 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier II Mouse 636 Genes GS84304: Hprt-ps1 (Published QTL, Chr 17)
Expand Tier I Human 1288 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1069 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 424 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier II Mouse 858 Genes GS136021: hematopoietic stem cell frequency regulator (Hscfr, Published QTL Chr 17)
Expand Tier II Human 10111 Genes GS235272: [MeSH] Membrane Proteins : D008565
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Mouse GO 10875 Genes GS181473: GO:0005488 binding
Expand Tier I Human 54 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Human 2115 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 943 Genes GS199468: GO:0006508 proteolysis
Expand Tier I Human 185 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse GO 5101 Genes GS192512: GO:0003824 catalytic activity
Expand Tier II Rat 669 Genes GS224593: Blood pressure QTL 102 (Bp102 Published QTL Chr 7)
Expand Tier II Human 14403 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 584 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 777 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 781 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 434 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 465 Genes GS229162: MSigDB Geneset - ACTGTGA,MIR-27A,MIR-27B
Expand Tier II Mouse 945 Genes GS136562: radiation pulmonary fibrosis 1 (Radpf1, Published QTL Chr 17)
Expand Tier II Mouse 947 Genes GS136429: pulmonary adenoma susceptibility 2 (Pas2, Published QTL Chr 17)
Expand Tier II Mouse 909 Genes GS135781: early growth adjusted QTL 2 (Egaq2, Published QTL Chr 17)
Expand Tier II Human 14645 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 17259 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier I Human 504 Genes GS229037: MSigDB Geneset - WTTGKCTG_UNKNOWN
Expand Tier II Human 12777 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Mouse 941 Genes GS135370: B.burgdorferi-associated arthritis 8 (Bbaa8, Published QTL Chr 17)
Expand Tier II Human 16451 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Human 39 Genes GS172678: HP:0009117 Aplasia/Hypoplasia of the maxilla
Expand Tier I Human 2 Genes GS173409: HP:0002682 Broad skull
Expand Tier I Human GO 553 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 184 Genes GS229701: MSigDB Geneset - GSE37416_CTRL_VS_48H_F_TULARENSIS_LVS_NEUTROPHIL_UP
Expand Tier II Mouse 891 Genes GS136866: T cell receptor induced activation 3 (Tria3, Published QTL Chr 17)
Expand Tier II Mouse 915 Genes GS136685: skull morphology 24 (Skull24, Published QTL Chr 17)
Expand Tier II Human 11159 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human 419 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 301 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 254 Genes GS229235: MSigDB Geneset - GTACTGT,MIR-101
Expand Tier II Human 8835 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier II Rat 527 Genes GS224868: Serum free fatty acids level QTL 5 (Sffal5 Published QTL Chr 7)
Expand Tier I Human 121 Genes GS175023: HP:0001629 Ventricular septal defect
Expand Tier I Human 310 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier II Human 19359 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier II Human 171 Genes GS241599: [MeSH] Thrombospondins : D019699
Expand Tier I Human GO 11880 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse GO 1040 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Mouse 194 Genes GS227853: MSigDB Geneset - GSE14350_TREG_VS_TEFF_IN_IL2RB_KO_UP
Expand Tier II Human 16876 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Mouse GO 7 Genes GS192979: GO:0001527 microfibril
Expand Tier I Human 39 Genes GS173054: HP:0000327 Hypoplasia of the maxilla
Expand Tier I Rat DRG 4708 Genes GS86932: Table S3: CORTEX 17K MICROARRAY [DRG]
Expand Tier II Human 11230 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 14014 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier II Human 7110 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier II Human 3235 Genes GS236860: [MeSH] Endopeptidases : D010450
Expand Tier I Human 297 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier II Mouse 890 Genes GS135896: gastritis type A susceptibility locus 4 (Gasa4, Published QTL Chr 17)
Expand Tier I Mouse GO 1823 Genes GS193270: GO:0005576 extracellular region
Expand Tier II Human 9485 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier II Rat 768 Genes GS223492: Polydactyly-luxate syndrome (PLS) morphotypes QTL 3 (Plsm3 Published QTL Chr 7)
Expand Tier II Mouse 684 Genes GS84299: ethanol metabolism rate (Published QTL, Chr 17)
Expand Tier I Human 2365 Genes GS175529: HP:0000001 All
Expand Tier I Human 4 Genes GS171856: HP:0000594 Shallow anterior chamber
Expand Tier I Human 117 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier III Mouse 629 Genes GS246339: suprachiasmatic nucleus (SCN) Hypermethlyated
Expand Tier I Human 16 Genes GS175270: HP:0001169 Broad palm
Expand Tier I Human GO 2333 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human 194 Genes GS232305: PC Geneset - "YTAATTAA_V$LHX3_01" pathway genes
Expand Tier II Human 661 Genes GS238687: [MeSH] Disease : D004194
Expand Tier I Human GO 3909 Genes GS198323: GO:0046872 metal ion binding
Expand Tier II Rat 744 Genes GS223830: Serum corticosterone level QTL 5 (Scort5 Published QTL Chr 7)
Expand Tier II Mouse 823 Genes GS129074: alloantigen response 1 (Alan1 Published QTL Chr 17)
Expand Tier II Human 646 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier II Mouse 643 Genes GS135962: HDL QTL 29 (Hdlq29, Published QTL Chr 17)
Expand Tier III Mouse 8264 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier II Mouse 915 Genes GS136549: proteinuria 2 (Ptnu2, Published QTL Chr 17)
Expand Tier I Human 357 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human CTD 696 Genes GS122755: Aldehydes interacting with Homo sapiens associated genes (MeSH:D000447) in CTD
Expand Tier I Human 180 Genes GS230217: MSigDB Geneset - GSE22045_TREG_VS_TCONV_DN
Expand Tier II Human 18339 Genes GS238575: [MeSH] Nucleic Acids : D009696
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 Mouse 259 Genes GS129090: bleomycin-induced pulmonary fibrosis 1 (Blmpf1 Published QTL Chr 17)
Expand Tier I Human 43 Genes GS173055: HP:0000326 Abnormality of the maxilla
Expand Tier II Mouse 948 Genes GS135644: cerebral malaria susceptibility in CBA/N (Cmcs, Published QTL Chr 17)
Expand Tier I Human 28 Genes GS175052: HP:0001083 Ectopia lentis
Expand Tier I Human 539 Genes GS227281: MSigDB Geneset - chr19p13
Expand Tier I Human 183 Genes GS229967: MSigDB Geneset - YTAATTAA_V$LHX3_01
Expand Tier II Human 10961 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Human 14 Genes GS171557: HP:0003416 Spinal canal stenosis
Expand Tier I Human GO 105 Genes GS199822: GO:0004222 metalloendopeptidase activity
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier II Human 17884 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Mouse GO 22819 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 3688 Genes GS241772: [MeSH] Carbohydrates : D002241
Expand Tier I Human 234 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier II Human 2091 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier II Mouse 915 Genes GS135877: femur geometry 14 (Fmgty14, Published QTL Chr 17)
Expand Tier II Human 15271 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human 31 Genes GS170915: HP:0006009 Broad phalanx
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 65 Genes GS171651: HP:0000618 Blindness
Expand Tier II Rat 678 Genes GS224419: Heart rate QTL 10 (Hrtrt10 Published QTL Chr 7)
Expand Tier II Human 1432 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Human GO 8649 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 204 Genes GS232041: PC Geneset - "V$RP58_01" pathway genes
Expand Tier II Human 18365 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 53 Genes GS174451: HP:0006705 Abnormality of the atrioventricular valves
Expand Tier II Mouse 919 Genes GS136260: male hybrid sterility QTL 1 (Mhstq1, Published QTL Chr 17)
Expand Tier II Human 5085 Genes GS237965: [MeSH] Peptide Hydrolases : D010447
Expand Tier II Human 4823 Genes GS239522: [MeSH] Growth : D006128
Expand Tier I Human GO 16873 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 515 Genes GS174081: HP:0004322 Short stature
Expand Tier II Human 17873 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 14315 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Mouse 678 Genes GS84303: differences in cocaine responsiveness (Published QTL, Chr 17)
Expand Tier II Human 789 Genes GS236184: [MeSH] Extracellular Space : D005110
Expand Tier II Human 5214 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier I Mouse GO 7642 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier II Human 11214 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier II Human 13809 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 16448 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier II Mouse 643 Genes GS136385: obesity and body weight QTL 4 (Obwq4, Published QTL Chr 17)
Expand Tier I Human GO 5284 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse GO 8070 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier II Human 16145 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human CTD 10572 Genes GS125506: Valproic Acid interacting with Homo sapiens associated genes (MeSH:D014635) in CTD
Expand Tier I Human CTD 3575 Genes GS124427: butyraldehyde interacting with Homo sapiens associated genes (MeSH:C018475) in CTD
Expand Tier II Human 311 Genes GS242611: [MeSH] ADAM Proteins : D051722
Expand Tier I Human 209 Genes GS175164: HP:0011927 Short digit
Expand Tier II Mouse 909 Genes GS136943: weight 6 weeks QTL 11 (W6q11, Published QTL Chr 17)
Expand Tier I Human 123 Genes GS175583: HP:0010438 Abnormality of the ventricular septum
Expand Tier II Human 11279 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier II Mouse 891 Genes GS136758: soft tissue heal 11 (Stheal11, Published QTL Chr 17)
Expand Tier II Human 7589 Genes GS242551: [MeSH] Physiological Processes : D055705
Expand Tier I Human 102 Genes GS173507: HP:0000520 Proptosis
Expand Tier I Human 1206 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human CTD 1467 Genes GS123541: pentanal interacting with Homo sapiens associated genes (MeSH:C046012) in CTD
Expand Tier II Mouse 900 Genes GS129089: bronchial hyperresponsiveness 3 (Bhr3 Published QTL Chr 17)
Expand Tier II Human 13275 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 412 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier II Mouse 947 Genes GS136962: weight adult 4 (Wta4, Published QTL Chr 17)
Expand Tier I Human 1563 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 77 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human 142 Genes GS174721: HP:0000772 Abnormality of the ribs
Expand Tier I Human 68 Genes GS176574: HP:0008062 Aplasia/Hypoplasia affecting the anterior segment of the eye
Expand Tier I Human GO 372 Genes GS209907: GO:0004175 endopeptidase activity
Expand Tier II Mouse 715 Genes GS135455: body weight 2 (Bodwt2, Published QTL Chr 17)
Expand Tier II Human 6771 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 179 Genes GS228689: MSigDB Geneset - GSE2706_R848_VS_R848_AND_LPS_8H_STIM_DC_DN
Expand Tier I Mouse GO 571 Genes GS188685: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 551 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier II Human 7908 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier II Human 5776 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 3607 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier I Mouse GO 360 Genes GS192965: GO:0004175 endopeptidase activity
Expand Tier I Human 17 Genes GS174141: HP:0005916 Abnormal metacarpal morphology
Expand Tier II Human 4645 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier II Human 1449 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier II Mouse 947 Genes GS136043: insulin dependent diabetes susceptibility 16 (Idd16, Published QTL Chr 17)
Expand Tier I Human GO 9416 Genes GS196943: GO:0008152 metabolic process
Expand Tier II Human 17895 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 52 Genes GS174808: HP:0001633 Abnormality of the mitral valve
Expand Tier I Human 55 Genes GS173685: HP:0001641 Abnormality of the pulmonary valve
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 I Human 45 Genes GS176166: HP:0001256 Intellectual disability, mild
Expand Tier II Human 229 Genes GS237839: [MeSH] Eye Abnormalities : D005124
Expand Tier I Human 188 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human CTD 283 Genes GS255384: glyphosate interacting with Salmo trutta associated genes (MeSH:C010974) in CTD
Expand Tier II Human 17896 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse CTD 1018 Genes GS255822: Magnetite Nanoparticles interacting with Mus musculus associated genes (MeSH:D058185) in CTD
Expand Tier II Mouse 891 Genes GS136177: locomotor activity 2 (Loco2, Published QTL Chr 17)
Expand Tier III Human 2223 Genes GS222813: The Druggable Gene Interaction Database
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Human GO 7309 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1099 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier II Human 9373 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703