Gene Details



ADAMTSL2 and homologs in 6 species are found in 481 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 98 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier II Human 2932 Genes GS236094: [MeSH] Scleroproteins : D012596
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 145 Genes GS171320: HP:0100360 Contractures of the joints of the upper limbs
Expand Tier I Human 241 Genes GS232559: PC Geneset - "V$MYOD_Q6" pathway genes
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Mouse 537 Genes GS136604: spinal bone mineral density 2 (Sbmd2, Published QTL Chr 2)
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human GO 871 Genes GS198861: GO:0007167 enzyme linked receptor protein signaling pathway
Expand Tier I Mouse 199 Genes GS230661: MSigDB Geneset - GSE30083_SP2_VS_SP3_THYMOCYTE_UP
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 7 Genes GS171530: HP:0001702 Abnormality of the tricuspid valve
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 171 Genes GS182225: GO:0008237 metallopeptidase activity
Expand Tier I Human 2254 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier I Mouse 545 Genes GS135847: femoral cross-sectional area 5 (Fcsa5, Published QTL Chr 2)
Expand Tier I Mouse GO 3537 Genes GS192041: GO:0043169 cation binding
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 179 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 244 Genes GS230710: MSigDB Geneset - V$MYOD_Q6
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier I Human 148 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Mouse 537 Genes GS136603: spinal bone mineral density 1 (Sbmd1, Published QTL Chr 2)
Expand Tier I Mouse GO 2678 Genes GS181892: GO:0048523 negative regulation of cellular process
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier III Rat 364 Genes GS223210: Gastric cancer resistance QTL 2 (Gcr2 Published QTL Chr 3)
Expand Tier I Human 7 Genes GS173407: HP:0002680 J-shaped sella turcica
Expand Tier II Human 15224 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier I Mouse 198 Genes GS227210: MSigDB Geneset - GSE30083_SP1_VS_SP2_THYMOCYTE_DN
Expand Tier I Human 246 Genes GS232154: PC Geneset - "V$CEBPGAMMA_Q6" pathway genes
Expand Tier I Human 47 Genes GS173284: HP:0000311 Round face
Expand Tier I Human 49 Genes GS173605: HP:0004426 Abnormality of the cheeks
Expand Tier I Human GO 2308 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human 167 Genes GS230697: MSigDB Geneset - GSE29614_CTRL_VS_DAY3_TIV_FLU_VACCINE_PBMC_DN
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 18 Genes GS173843: HP:0002777 Tracheal stenosis
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 88 Genes GS174323: HP:0004414 Abnormality of the pulmonary artery
Expand Tier I Human 184 Genes GS229372: MSigDB Geneset - GSE12366_NAIVE_VS_MEMORY_BCELL_UP
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Rat 439 Genes GS128037: Alcohol consumption QTL 8 (Alc8, Published QTL, Chr 3)
Expand Tier I Human 198 Genes GS230180: MSigDB Geneset - GSE3982_BASOPHIL_VS_EFF_MEMORY_CD4_TCELL_UP
Expand Tier I Human 43 Genes GS175611: HP:0002092 Pulmonary hypertension
Expand Tier I Mouse GO 3311 Genes GS192279: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human 2430 Genes GS231626: PC Geneset - "CAGGTG_V$E12_Q6" pathway genes
Expand Tier I Mouse GO 40 Genes GS187392: GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
Expand Tier III Rat 512 Genes GS224019: Serum cholesterol level QTL 62 (Scl62 Published QTL Chr 3)
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier II Human 6012 Genes GS236915: [MeSH] Genome, Human : D015894
Expand Tier I Mouse GO 588 Genes GS189483: GO:0023057 negative regulation of signaling
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 66 Genes GS176033: HP:0011039 Abnormality of the helix
Expand Tier I Human 257 Genes GS227162: MSigDB Geneset - V$E12_Q6
Expand Tier I Human 20 Genes GS171556: HP:0001387 Joint stiffness
Expand Tier I Human GO 2026 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Mouse 543 Genes GS136612: colon tumor susceptibility 2 (Scc2, Published QTL Chr 2)
Expand Tier I Human 10 Genes GS173408: HP:0002681 Deformed sella turcica
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 1833 Genes GS184324: GO:0010646 regulation of cell communication
Expand Tier I Mouse 247 Genes GS129114: collagen induced arthritis QTL 4 (Cia4 Published QTL Chr 2)
Expand Tier I Mouse GO 69 Genes GS177223: GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Mouse GO 2994 Genes GS186215: GO:0048519 negative regulation of biological process
Expand Tier I Human 1443 Genes GS232484: PC Geneset - "CAGCTG_V$AP4_Q5" pathway genes
Expand Tier I Human 164 Genes GS171654: HP:0003121 Limb joint contracture
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 20 Genes GS172151: HP:0002673 Coxa valga
Expand Tier I Human 911 Genes GS228818: MSigDB Geneset - GCANCTGNY_V$MYOD_Q6
Expand Tier I Human 21 Genes GS173291: HP:0000319 Smooth philtrum
Expand Tier I Mouse GO 3442 Genes GS181533: GO:0046872 metal ion binding
Expand Tier II Human 8197 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier II Mouse 453 Genes GS84122: ethanol conditioned taste aversion (Published QTL, Chr 2)
Expand Tier II Mouse 454 Genes GS84123: METH responses for climbing (Published QTL, Chr 2)
Expand Tier I Human 219 Genes GS230077: MSigDB Geneset - MORF_BCL2
Expand Tier I Human 12 Genes GS175022: HP:0001620 High pitched voice
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human GO 165 Genes GS210361: GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier I Human 2460 Genes GS229573: MSigDB Geneset - CAGGTG_V$E12_Q6
Expand Tier I Mouse GO 548 Genes GS188289: GO:0009968 negative regulation of signal transduction
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Human 228 Genes GS229812: MSigDB Geneset - chr9q34
Expand Tier I Mouse GO 1828 Genes GS189485: GO:0023051 regulation of signaling
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human 110 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human GO 777 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 207 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier III Rat 165 Genes GS224578: Estrogen-induced pituitary tumorigenesis QTL 17 (Ept17 Published QTL Chr 3)
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Mouse 537 Genes GS136522: platelet quantitative locus 1 (Pltq1, Published QTL Chr 2)
Expand Tier I Mouse 459 Genes GS135533: cobblestone area-forming cell number QTL 1 (Cafcnq1, Published QTL Chr 2)
Expand Tier I Human 40 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
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 I Human 1513 Genes GS231868: PC Geneset - "Metabolism of proteins" pathway genes
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 676 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Mouse 548 Genes GS136471: periosteal circumference and femur length 1 (Pcfm1, Published QTL Chr 2)
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier I Human 223 Genes GS227343: MSigDB Geneset - MORF_FDXR
Expand Tier I Mouse 548 Genes GS135816: ethanol induced ataxia 3 (Etax3, Published QTL Chr 2)
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 150 Genes GS174920: HP:0000766 Abnormality of the sternum
Expand Tier I Human 257 Genes GS232108: PC Geneset - "V$IPF1_Q4" pathway genes
Expand Tier I Human GO 267 Genes GS204628: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Mouse 199 Genes GS227936: MSigDB Geneset - GSE27786_CD4_TCELL_VS_MONO_MAC_DN
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
Expand Tier II Human 2632 Genes GS242312: [MeSH] Extracellular Matrix Proteins : D016326
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 127 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 89 Genes GS193946: GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier III Mouse 6189 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 97 Genes GS174919: HP:0000767 Pectus excavatum
Expand Tier I Human 25 Genes GS173340: HP:0003368 Abnormality of the femoral head
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 17 Genes GS173461: HP:0001650 Aortic valve stenosis
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human 165 Genes GS227396: MSigDB Geneset - MORF_FANCG
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 263 Genes GS232532: PC Geneset - "V$AP1_Q2_01" pathway genes
Expand Tier I Human 84 Genes GS230325: MSigDB Geneset - MORF_RBM8A
Expand Tier I Human 27 Genes GS171097: HP:0006499 Abnormality of femoral epiphyses
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier I Mouse GO 5225 Genes GS189860: GO:0043167 ion binding
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Mouse GO 2190 Genes GS191129: GO:0016787 hydrolase activity
Expand Tier I Mouse 469 Genes GS136890: voluntary alcohol consumption QTL 4 (Vacq4, Published QTL Chr 2)
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Human 54 Genes GS175896: HP:0000938 Osteopenia
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human 79 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Human 253 Genes GS229489: MSigDB Geneset - V$IPF1_Q4
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse GO 5654 Genes GS182325: GO:0051716 cellular response to stimulus
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 15356 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier I Mouse 3092 Genes GS128575: Ethanol induced LORR Chr# 2
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 Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse 198 Genes GS228948: MSigDB Geneset - GSE13306_TREG_VS_TCONV_SPLEEN_UP
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse 200 Genes GS229123: MSigDB Geneset - GSE36392_TYPE_2_MYELOID_VS_MAC_IL25_TREATED_LUNG_UP
Expand Tier I Human 112 Genes GS171616: HP:0100490 Camptodactyly of finger
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 I Human 244 Genes GS228933: MSigDB Geneset - MORF_MT4
Expand Tier I Human 66 Genes GS172110: HP:0002983 Micromelia
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 83 Genes GS172316: HP:0003026 Short long bones
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier I Human 127 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier I Mouse 338 Genes GS129163: proteoglycan induced spondylitis 2 (Pgis2 Published QTL Chr 2)
Expand Tier I Human 2 Genes GS177012: HP:0010446 Tricuspid stenosis
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier I Mouse GO 75 Genes GS189382: GO:0090101 negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 10 Genes GS176969: HP:0005003 Aplasia/Hypoplasia of the capital femoral epiphysis
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Human 254 Genes GS228919: MSigDB Geneset - V$TATA_01
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 550 Genes GS205544: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 155 Genes GS228048: MSigDB Geneset - MORF_DDX11
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier II Human 12085 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier I Mouse 446 Genes GS135721: variability in response to cholestrol enriched atherogenic diet (Diet1, Published QTL Chr 2)
Expand Tier I Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Human 60 Genes GS174139: HP:0005914 Aplasia/Hypoplasia involving the metacarpal bones
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human GO 93 Genes GS206245: GO:0090101 negative regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human 110 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Human 54 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Human 552 Genes GS230558: MSigDB Geneset - YCATTAA_UNKNOWN
Expand Tier I Human 7 Genes GS175938: HP:0100830 Round ear
Expand Tier I Mouse 333 Genes GS135244: adiposity 10 (Adip10, Published QTL Chr 2)
Expand Tier I Human 246 Genes GS231646: PC Geneset - "V$E12_Q6" pathway genes
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier II Human 24024 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier I Human 296 Genes GS174145: HP:0005918 Abnormality of phalanx of finger
Expand Tier I Mouse GO 6947 Genes GS192918: GO:0050896 response to stimulus
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Human 145 Genes GS228824: MSigDB Geneset - MORF_LTK
Expand Tier I Human 9 Genes GS171748: HP:0001718 Mitral stenosis
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4065 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human 107 Genes GS229176: MSigDB Geneset - MORF_CNTN1
Expand Tier I Human 116 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier I Human 1279 Genes GS229869: MSigDB Geneset - TATAAA_V$TATA_01
Expand Tier I Human 65 Genes GS171559: HP:0000388 Otitis media
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier III Rat 165 Genes GS223557: Estrogen-induced pituitary tumorigenesis QTL 6 (Ept6 Published QTL Chr 3)
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 130 Genes GS173970: HP:0009473 Joint contracture of the hand
Expand Tier I Human 47 Genes GS174089: HP:0003367 Abnormality of the femoral neck
Expand Tier I Human 110 Genes GS176480: HP:0009826 Hypoplasia involving bones of the extremities
Expand Tier I Human GO 167 Genes GS204627: GO:0007179 transforming growth factor beta receptor signaling pathway
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse 539 Genes GS136035: induction of brown adipocytes 6 (Iba6, Published QTL Chr 2)
Expand Tier II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier I Mouse 542 Genes GS136087: lean body mass 1 (Lbm1, Published QTL Chr 2)
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 193 Genes GS227851: MSigDB Geneset - GSE9006_1MONTH_VS_4MONTH_POST_TYPE_1_DIABETES_DX_PBMC_DN
Expand Tier I Human 420 Genes GS230124: MSigDB Geneset - TGGNNNNNNKCCAR_UNKNOWN
Expand Tier I Human 175 Genes GS227136: MSigDB Geneset - GSE29614_CTRL_VS_TIV_FLU_VACCINE_PBMC_2007_DN
Expand Tier III Rat 457 Genes GS223892: Alcohol consumption QTL 19 (Alc19 Published QTL Chr 3)
Expand Tier I Human GO 105 Genes GS199822: GO:0004222 metalloendopeptidase activity
Expand Tier II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Human 60 Genes GS229205: MSigDB Geneset - MORF_PTPN9
Expand Tier I Human GO 2020 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Mouse GO 113 Genes GS187767: GO:0007179 transforming growth factor beta receptor signaling pathway
Expand Tier I Human 252 Genes GS232479: PC Geneset - "V$MTF1_Q4" pathway genes
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 102 Genes GS173545: HP:0010647 Abnormal elasticity of skin
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 75 Genes GS176150: HP:0003019 Abnormality of the wrist
Expand Tier I Human 136 Genes GS227339: MSigDB Geneset - MORF_IKBKG
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 320 Genes GS231746: PC Geneset - "CCCNNGGGAR_V$OLF1_01" pathway genes
Expand Tier I Human 93 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 49 Genes GS175305: HP:0000293 Full cheeks
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier III Rat 415 Genes GS224667: Aerobic running capacity QTL 3 (Arunc3 Published QTL Chr 3)
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 53 Genes GS174451: HP:0006705 Abnormality of the atrioventricular valves
Expand Tier I Human 32 Genes GS176416: HP:0100679 Lack of skin elasticity
Expand Tier I Human 249 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Mouse GO 710 Genes GS189324: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse GO 146 Genes GS193417: GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier II Mouse 468 Genes GS84124: ethanol consumption (Published QTL, Chr 2)
Expand Tier II Human 8647 Genes GS242147: [MeSH] Fibroblasts : D005347
Expand Tier I Human 1498 Genes GS230639: MSigDB Geneset - CAGCTG_V$AP4_Q5
Expand Tier I Human 8 Genes GS172165: HP:0001239 Wrist flexion contracture
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
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 I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Mouse 550 Genes GS136074: insulin QTL 7 (Insq7, Published QTL Chr 2)
Expand Tier I Mouse 459 Genes GS135441: bone marrow graft rejection 2 (Bmgr2, Published QTL Chr 2)
Expand Tier I Human 117 Genes GS170853: HP:0006261 Abnormality of phalangeal joints of the hand
Expand Tier III Rat 474 Genes GS224899: Alcohol consumption QTL 8 (Alc8 Published QTL Chr 3)
Expand Tier I Human 208 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 145 Genes GS230395: MSigDB Geneset - MORF_RAGE
Expand Tier I Human 2227 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Human 171 Genes GS227164: MSigDB Geneset - GSE10463_CD40L_AND_VA347_VS_CD40L_IN_DC_DN
Expand Tier I Human 10 Genes GS174480: HP:0010577 Absent epiphyses
Expand Tier I Human 112 Genes GS171810: HP:0005651 Flexion contracture of finger
Expand Tier I Human 102 Genes GS229119: MSigDB Geneset - MORF_CASP2
Expand Tier I Human 1 Genes GS172520: HP:0006161 Short metacarpals with rounded proximal ends
Expand Tier I Human CTD 1541 Genes GS125445: Phenobarbital interacting genes (MeSH:D010634) in CTD
Expand Tier I Human 143 Genes GS229043: MSigDB Geneset - MORF_PML
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 27 Genes GS175661: HP:0006500 Abnormality involving the epiphyses of the lower limbs
Expand Tier I Human 173 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 13 Genes GS172154: HP:0002679 Abnormality of the sella turcica
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 82 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 54 Genes GS175733: HP:0010049 Short metacarpal
Expand Tier I Rat 421 Genes GS128039: Alcohol consumption QTL 19 (Alc19, Published QTL, Chr 3)
Expand Tier I Human 76 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Mouse GO 592 Genes GS187168: GO:0010648 negative regulation of cell communication
Expand Tier I Human GO 370 Genes GS209907: GO:0004175 endopeptidase activity
Expand Tier I Human GO 65 Genes GS204254: GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 239 Genes GS227815: MSigDB Geneset - V$SMAD3_Q6
Expand Tier I Mouse GO 571 Genes GS188685: GO:0070011 peptidase activity, acting on L-amino acid peptides
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 181 Genes GS228453: MSigDB Geneset - GSE37416_CTRL_VS_0H_F_TULARENSIS_LVS_NEUTROPHIL_UP
Expand Tier I Mouse GO 230 Genes GS187768: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 320 Genes GS229856: MSigDB Geneset - CCCNNGGGAR_V$OLF1_01
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 5399 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier I Mouse GO 360 Genes GS192965: GO:0004175 endopeptidase activity
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human 8 Genes GS173132: HP:0003090 Hypoplasia of the capital femoral epiphysis
Expand Tier I Human 1 Genes GS173489: HP:0005041 Irregular capital femoral epiphysis
Expand Tier III Mouse 8151 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Mouse GO 5111 Genes GS187146: GO:0044700 single organism signaling
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier I Mouse 549 Genes GS136554: pentylenetetrazol induced seizure susceptibility 1b (Ptz1b, Published QTL Chr 2)
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 107 Genes GS171228: HP:0002823 Abnormality of the femur
Expand Tier I Human 273 Genes GS229913: MSigDB Geneset - V$AP1_Q2_01
Expand Tier I Human 52 Genes GS174808: HP:0001633 Abnormality of the mitral valve
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse GO 577 Genes GS182069: GO:0007167 enzyme linked receptor protein signaling pathway
Expand Tier I Mouse GO 1575 Genes GS188290: GO:0009966 regulation of signal transduction
Expand Tier I Human GO 679 Genes GS204029: GO:0010648 negative regulation of cell communication
Expand Tier I Human 187 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 243 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human 210 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 60 Genes GS170970: HP:0000154 Wide mouth
Expand Tier I Human 43 Genes GS174688: HP:0004890 Elevated pulmonary artery pressure
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier II Human 15607 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier I Human GO 2321 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Mouse 338 Genes GS135222: aromatase activity QTL 3 (Aaiq3, Published QTL Chr 2)
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human GO 178 Genes GS199022: GO:0008237 metallopeptidase activity
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 I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 209 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human 813 Genes GS231668: PC Geneset - "TGACAGNY_V$MEIS1_01" pathway genes
Expand Tier I Mouse 537 Genes GS136515: plasma plant sterol 2a (Plast2a, Published QTL Chr 2)
Expand Tier I Human GO 572 Genes GS199006: GO:0008233 peptidase activity
Expand Tier III Rat 459 Genes GS223426: Blood pressure QTL 15 (Bp15 Published QTL Chr 3)
Expand Tier I Human 253 Genes GS229436: MSigDB Geneset - V$CEBPGAMMA_Q6
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 195 Genes GS230604: MSigDB Geneset - GSE29618_PRE_VS_DAY7_FLU_VACCINE_BCELL_UP
Expand Tier I Human 187 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 178 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Mouse 459 Genes GS136228: mandible length 2 (Manln2, Published QTL Chr 2)
Expand Tier I Mouse 196 Genes GS230199: MSigDB Geneset - GSE13306_TREG_VS_TCONV_UP
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 252 Genes GS230636: MSigDB Geneset - V$MTF1_Q4
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 85 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 169 Genes GS230772: MSigDB Geneset - TAAYNRNNTCC_UNKNOWN
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human 937 Genes GS230176: MSigDB Geneset - TTANTCA_UNKNOWN
Expand Tier I Human 818 Genes GS227182: MSigDB Geneset - TGACAGNY_V$MEIS1_01
Expand Tier I Mouse GO 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse GO 4725 Genes GS192265: GO:0007165 signal transduction
Expand Tier I Human GO 1770 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier III Rat 1265 Genes GS224435: Serum cholesterol level QTL 56 (Scl56 Published QTL Chr 3)
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Human 10 Genes GS171365: HP:0000391 Thickened helices
Expand Tier I Mouse 469 Genes GS135851: fecundity QTL 1 (Fecq1, Published QTL Chr 2)
Expand Tier II Human 13620 Genes GS234949: [MeSH] Genetic Vectors : D005822
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Human 113 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 25 Genes GS173494: HP:0010574 Abnormality of the epiphysis of the femoral head
Expand Tier I Mouse GO 2030 Genes GS189326: GO:0048583 regulation of response to stimulus
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
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 94 Genes GS174879: HP:0002104 Apnea
Expand Tier II Human 32928 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier I Human 60 Genes GS174088: HP:0003366 Abnormality of the femoral neck and head region
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 41 Genes GS172655: HP:0001792 Small nail
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
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 I Mouse GO 1341 Genes GS186836: GO:0008270 zinc ion binding
Expand Tier I Human 113 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Human 30 Genes GS229608: MSigDB Geneset - CAR_TNFRSF25
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
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 I Human GO 361 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 50 Genes GS171995: HP:0001764 Small feet
Expand Tier II Human 13600 Genes GS235415: [MeSH] Embryo, Mammalian : D004622
Expand Tier I Human 248 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 66 Genes GS172588: HP:0001831 Short toe
Expand Tier I Human 236 Genes GS232448: PC Geneset - "V$SMAD3_Q6" pathway genes
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Human 73218 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Human 900 Genes GS232535: PC Geneset - "GCANCTGNY_V$MYOD_Q6" pathway genes
Expand Tier I Mouse 469 Genes GS135820: ethanol consumption 1 (Etohc1, Published QTL Chr 2)
Expand Tier I Human 135 Genes GS229458: MSigDB Geneset - KRAS.KIDNEY_UP.V1_DN
Expand Tier I Mouse 448 Genes GS136889: voluntary alcohol consumption QTL 3 (Vacq3, Published QTL Chr 2)
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 45 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human GO 635 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 211 Genes GS228238: MSigDB Geneset - MORF_RBBP8
Expand Tier III Rat 364 Genes GS223663: Stress Responsive Cort Basal QTL 1 (Srcrtb1 Published QTL Chr 3)
Expand Mouse 740 Genes GS247754: 773 ProbeSets imported from Genenetwork
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 147 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier II Human 15662 Genes GS235446: [MeSH] Reproductive and Urinary Physiological Phenomena : D012101
Expand Tier I Human 260 Genes GS229602: MSigDB Geneset - MORF_TNFRSF25
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier II Human 11555 Genes GS234570: [MeSH] Cell Differentiation : D002454
Expand Tier III Rat 459 Genes GS224504: Blood pressure QTL 85 (Bp85 Published QTL Chr 3)
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier III Rat 455 Genes GS224366: Cardiac mass QTL 10 (Cm10 Published QTL Chr 3)
Expand Tier I Human 46 Genes GS175664: HP:0006505 Abnormality involving the epiphyses of the limbs
Expand Tier III Rat 501 Genes GS224214: Bone structure and strength QTL 95 (Bss95 Published QTL Chr 3)
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 220 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process