Gene Details



SH3TC2 and homologs in 6 species are found in 519 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 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Human 1 Genes GS172331: HP:0004466 Prolonged brainstem auditory evoked potentials
Expand Tier II Human 1054 Genes GS242472: [MeSH] src Homology Domains : D018909
Expand Tier I Mouse 239 Genes GS136725: susceptibility to lung cancer 28 (Sluc28, Published QTL Chr 18)
Expand Tier I Human GO 406 Genes GS199582: GO:0016044 cellular membrane organization
Expand Tier I Mouse MP 1698 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier III Human 1987 Genes GS246374: Differential Expression Hippocampi Human Cocaine Addicts
Expand Tier III Human 2616 Genes GS218390: Alcoholism Susceptibility Chr 1
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 III Rat 268 Genes GS224806: Blood pressure QTL 319 (Bp319 Published QTL Chr 18)
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier III Rat 153 Genes GS223312: Blood pressure QTL 227 (Bp227 Published QTL Chr 18)
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 63 Genes GS175213: HP:0003693 Distal amyotrophy
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier II Mouse 235 Genes GS84311: high-dose ethanol actions (Published QTL, Chr 18)
Expand Tier I Human 2254 Genes GS230495: MSigDB Geneset - GGGAGGRR_V$MAZ_Q6
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 267 Genes GS135266: age-related hearing loss 6 (Ahl6, Published QTL Chr 18)
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier II Human 70216 Genes GS235234: [MeSH] Biochemical Phenomena : D001669
Expand Tier II Human 31959 Genes GS237114: [MeSH] Regulatory Elements, Transcriptional : D050436
Expand Tier III Rat 149 Genes GS224867: Body weight QTL 27 (Bw27 Published QTL Chr 18)
Expand Tier I Human GO 648 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Mouse 405 Genes GS135307: angle of entrainment 3 (Angle3, Published QTL Chr 18)
Expand Tier I Human GO 410 Genes GS201052: GO:0061024 membrane organization
Expand Tier II Human 9487 Genes GS243358: [MeSH] Protein Transport : D021381
Expand Tier I Mouse GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Human 11446 Genes GS236912: [MeSH] Biological Transport : D001692
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Human GO 2499 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier III Rat 117 Genes GS223318: Blood pressure QTL 229 (Bp229 Published QTL Chr 18)
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 135 Genes GS170969: HP:0000157 Abnormality of the tongue
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 18 Genes GS173678: HP:0003383 Onion bulb formation
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human GO 70 Genes GS202683: GO:0021782 glial cell development
Expand Tier I Human GO 833 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier III Rat 422 Genes GS223382: Bone mineral density QTL 65 (Bmd65 Published QTL Chr 18)
Expand Tier III Rat 361 Genes GS223895: Abdominal fat weight QTL 8 (Abfw8 Published QTL Chr 18)
Expand Tier I Mouse 165 Genes GS129162: proteoglycan induced spondylitis 1 (Pgis1 Published QTL Chr 18)
Expand Tier I Mouse MP 2893 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier III Rat 502 Genes GS223693: Estrogen-induced mammary cancer QTL 2 (Emca2 Published QTL Chr 18)
Expand Tier II Human 6012 Genes GS236915: [MeSH] Genome, Human : D015894
Expand Tier I Human 25 Genes GS173680: HP:0003380 Decreased number of peripheral myelinated nerve fibers
Expand Tier III Rat 443 Genes GS223281: Blood pressure QTL 353 (Bp353 Published QTL Chr 18)
Expand Tier I Human 186 Genes GS228675: MSigDB Geneset - RPS14_DN.V1_DN
Expand Tier III Rat 350 Genes GS224440: Body weight QTL 92 (Bw92 Published QTL Chr 18)
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 198 Genes GS227720: MSigDB Geneset - GSE24634_IL4_VS_CTRL_TREATED_NAIVE_CD4_TCELL_DAY5_DN
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier II Human 143 Genes GS241948: [MeSH] Founder Effect : D018703
Expand Tier III Rat 153 Genes GS223414: Blood pressure QTL 349 (Bp349 Published QTL Chr 18)
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier III Rat 176 Genes GS224871: Sensitivity to stroke QTL 5 (Strs5 Published QTL Chr 18)
Expand Tier I Human 8 Genes GS174415: HP:0003484 Upper limb muscle weakness
Expand Tier II Human 1442 Genes GS235841: [MeSH] Peripheral Nerves : D010525
Expand Tier II Human 888 Genes GS239294: [MeSH] Heredodegenerative Disorders, Nervous System : D020271
Expand Tier I Mouse MP 243 Genes GS170569: MP:0005404 abnormal axon morphology
Expand Tier I Mouse GO 658 Genes GS192669: GO:0055082 cellular chemical homeostasis
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 3615 Genes GS178359: GO:0071840 cellular component organization or biogenesis
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier III Rat 490 Genes GS223279: Blood pressure QTL 355 (Bp355 Published QTL Chr 18)
Expand Tier II Human 439 Genes GS241760: [MeSH] Nerve Tissue : D009417
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier I Human 244 Genes GS227684: MSigDB Geneset - V$LMO2COM_02
Expand Tier III Rat 397 Genes GS224150: Glucose level QTL 68 (Gluco68 Published QTL Chr 18)
Expand Tier II Human 3578 Genes GS243730: [MeSH] Cytoplasmic Vesicles : D022162
Expand Tier I Human 7 Genes GS173467: HP:0001308 Tongue fasciculations
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Human 123 Genes GS220035: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human GO 98 Genes GS204614: GO:0019228 regulation of action potential in neuron
Expand Tier I Mouse GO 18 Genes GS179705: GO:0014044 Schwann cell development
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Human 123 Genes GS220904: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Human 366 Genes GS232379: PC Geneset - "WGGAATGY_V$TEF1_Q6" pathway genes
Expand Tier I Mouse 248 Genes GS135403: body growth late QTL 12 (Bglq12, Published QTL Chr 18)
Expand Tier I Mouse 251 Genes GS135651: cocaine induced activation 14 (Cocia14, Published QTL Chr 18)
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier III Rat 320 Genes GS223348: Hepatocarcinoma resistance QTL 14 (Hcar14 Published QTL Chr 18)
Expand Tier I Mouse 289 Genes GS136821: triglyceride QTL 1 (Tgq1, Published QTL Chr 18)
Expand Tier I Human GO 17 Genes GS208537: GO:0032292 peripheral nervous system axon ensheathment
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier I Human 27 Genes GS171008: HP:0011096 Peripheral demyelination
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 12802 Genes GS237481: [MeSH] Recombination, Genetic : D011995
Expand Tier II Human 8660 Genes GS239079: [MeSH] Cell Membrane : D002462
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 6533 Genes GS244610: [MeSH] Nervous System Diseases : D009422
Expand Tier I Human 96 Genes GS172854: HP:0004302 Functional motor problems.
Expand Tier I Human 1 Genes GS172705: HP:0007686 Abnormal pupillary function
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier II Human 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Human 9 Genes GS171322: HP:0008944 Distal lower limb amyotrophy
Expand Tier III Rat 698 Genes GS223145: Bone structure and strength QTL 21 (Bss21 Published QTL Chr 18)
Expand Tier I Human GO 96 Genes GS198898: GO:0007009 plasma membrane organization
Expand Tier II Human 2552 Genes GS243025: [MeSH] Neuroglia : D009457
Expand Human 123 Genes GS221330: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Mouse GO 2172 Genes GS180156: GO:0065008 regulation of biological quality
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier II Human 16067 Genes GS239024: [MeSH] Cytoplasmic Structures : D022083
Expand Tier I Mouse GO 5111 Genes GS189484: GO:0023052 signaling
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 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier II Human 550 Genes GS242475: [MeSH] Schwann Cells : D012583
Expand Tier I Human GO 752 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Mouse MP 3159 Genes GS169828: MP:0005386 behavior/neurological phenotype
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier III Mouse 7843 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human 688 Genes GS232672: PC Geneset - "YTATTTTNR_V$MEF2_02" pathway genes
Expand Tier I Human 121 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 8 Genes GS173506: HP:0009053 Distal lower limb muscle weakness
Expand Tier I Human GO 248 Genes GS194078: GO:0042391 regulation of membrane potential
Expand Tier II Human 59585 Genes GS234621: [MeSH] Chemical Actions and Uses : D020164
Expand Tier II Human 62071 Genes GS235061: [MeSH] Amino Acids, Peptides, and Proteins : D000602
Expand Tier II Human 16797 Genes GS241667: [MeSH] Cytoplasm : D003593
Expand Tier I Mouse GO 851 Genes GS180142: GO:0048878 chemical homeostasis
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier III Rat 347 Genes GS224229: Collagen induced arthritis QTL 17 (Cia17 Published QTL Chr 18)
Expand Tier I Mouse 421 Genes GS136615: colon tumor susceptibility 5 (Scc5, Published QTL Chr 18)
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier I Mouse GO 563 Genes GS187747: GO:0019226 transmission of nerve impulse
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 10 Genes GS172451: HP:0007210 Lower limb amyotrophy
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human GO 74 Genes GS206352: GO:0055037 recycling endosome
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Mouse GO 737 Genes GS183767: GO:0019725 cellular homeostasis
Expand Tier II Human 67 Genes GS236373: [MeSH] Charcot-Marie-Tooth Disease : D002607
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier III Rat 387 Genes GS224517: Body weight QTL 110 (Bw110 Published QTL Chr 18)
Expand Human 123 Genes GS221081: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Mouse GO 102 Genes GS190680: GO:0007272 ensheathment of neurons
Expand Tier III Rat 251 Genes GS223315: Blood pressure QTL 224 (Bp224 Published QTL Chr 18)
Expand Tier I Human 135 Genes GS172857: HP:0004305 Involuntary movements
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 19302 Genes GS236470: [MeSH] DNA-Binding Proteins : D004268
Expand Tier III Rat 161 Genes GS224713: Experimental allergic encephalomyelitis QTL y (Eaey Published QTL Chr 18)
Expand Tier I Mouse GO 102 Genes GS192188: GO:0008366 axon ensheathment
Expand Tier I Mouse GO 323 Genes GS184244: GO:0061024 membrane organization
Expand Tier I Mouse MP 2283 Genes GS169391: MP:0002066 abnormal motor capabilities/coordination/movement
Expand Tier III Rat 187 Genes GS224279: Serum aldosterone level QTL 2 (Sald2 Published QTL Chr 18)
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse MP 864 Genes GS169390: MP:0002067 abnormal sensory capabilities/reflexes/nociception
Expand Tier III Rat 591 Genes GS223448: Blood pressure QTL 233 (Bp233 Published QTL Chr 18)
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 22 Genes GS171659: HP:0000615 Abnormality of the pupil
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse 430 Genes GS136484: plasmacytoma susceptibility 6 (Pcyts6, Published QTL Chr 18)
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 169 Genes GS228583: MSigDB Geneset - SRC_UP.V1_DN
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Mouse GO 134 Genes GS187579: GO:0010001 glial cell differentiation
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 24 Genes GS176061: HP:0002355 Difficulty walking
Expand Tier II Human 2379 Genes GS243535: [MeSH] Neurodegenerative Diseases : D019636
Expand Tier II Human 6250 Genes GS244797: [MeSH] Disease Susceptibility : D004198
Expand Tier I Mouse GO 3614 Genes GS180229: GO:0005886 plasma membrane
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human 243 Genes GS231711: PC Geneset - "V$NERF_Q2" pathway genes
Expand Tier III Rat 361 Genes GS224179: Epididymal fat weight QTL 12 (Epfw12 Published QTL Chr 18)
Expand Tier I Mouse GO 587 Genes GS185880: GO:0035637 multicellular organismal signaling
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
Expand Tier II Human 32929 Genes GS243578: [MeSH] Reading Frames : D016364
Expand Tier I Human GO 83 Genes GS207579: GO:0007272 ensheathment of neurons
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier III Rat 153 Genes GS223439: Blood pressure QTL 238 (Bp238 Published QTL Chr 18)
Expand Tier III Rat 153 Genes GS223283: Blood pressure QTL 351 (Bp351 Published QTL Chr 18)
Expand Tier I Mouse GO 16 Genes GS193125: GO:0022011 myelination in peripheral nervous system
Expand Tier I Mouse MP 628 Genes GS164023: MP:0001961 abnormal reflex
Expand Tier II Human 1127 Genes GS239986: [MeSH] Neuromuscular Diseases : D009468
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier II Human 757 Genes GS238979: [MeSH] Nervous System Malformations : D009421
Expand Tier I Mouse GO 487 Genes GS191180: GO:0005768 endosome
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier I Human GO 10 Genes GS207330: GO:0043217 myelin maintenance
Expand Tier II Mouse 122 Genes GS35298: Neocortex Gene expression correlates of Prepulse inhibition at 85db in Males BXD
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier III Rat 397 Genes GS223848: Serum corticosterone level QTL 22 (Scort22 Published QTL Chr 18)
Expand Tier II Human 3385 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Human GO 144 Genes GS204441: GO:0010001 glial cell differentiation
Expand Tier II Human 2272 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier I Mouse 433 Genes GS136622: Stem cell proliferation 10 (Scpro10, Published QTL Chr 18)
Expand Tier I Mouse 391 Genes GS135255: adiposity 8 (Adip8, Published QTL Chr 18)
Expand Tier III Rat 251 Genes GS223314: Blood pressure QTL 225 (Bp225 Published QTL Chr 18)
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier II Human 446 Genes GS238178: [MeSH] Peripheral Nervous System Diseases : D010523
Expand Tier III Human 1701 Genes GS246373: Differential Expression Hippocampi Human Alcoholic
Expand Tier I Human 21 Genes GS174553: HP:0002380 Fasciculations
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
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 Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier I Human 62 Genes GS172355: HP:0002460 Distal muscle weakness
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 189 Genes GS229497: MSigDB Geneset - TGFB_UP.V1_DN
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 2227 Genes GS232290: PC Geneset - "GGGAGGRR_V$MAZ_Q6" pathway genes
Expand Tier I Human GO 19 Genes GS196464: GO:0014044 Schwann cell development
Expand Tier I Mouse GO 57 Genes GS185847: GO:0021782 glial cell development
Expand Tier II Human 2092 Genes GS235351: [MeSH] Transport Vesicles : D022161
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Human GO 1185 Genes GS207015: GO:0042592 homeostatic process
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier I Mouse 427 Genes GS136541: psoriasis susceptibility 7 (Psrs7, Published QTL Chr 18)
Expand Tier I Mouse 301 Genes GS135424: bleomycin-induced pulmonary fibrosis 5 (Blmpf5, Published QTL Chr 18)
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier II Human 13987 Genes GS237817: [MeSH] Cell Line, Tumor : D045744
Expand Tier I Human 1 Genes GS176888: HP:0007695 Abnormal pupillary light reflex
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier II Human 405 Genes GS237941: [MeSH] Chromosomes, Human, Pair 5 : D002895
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 27 Genes GS172613: HP:0003477 Peripheral axonal neuropathy
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse 221 Genes GS135757: experimental allergic encephalomyelitis susceptibility 25 (Eae25, Published QTL Chr 18)
Expand Tier I Mouse 399 Genes GS136281: modifier of engrailed QTL 1 (Moen1, Published QTL Chr 18)
Expand Tier II Human 1296 Genes GS244872: [MeSH] Endosomes : D011992
Expand Tier I Mouse GO 167 Genes GS184927: GO:0001508 regulation of action potential
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 I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier III Rat 423 Genes GS224604: Serum protein level QTL 1 (Sprol1 Published QTL Chr 18)
Expand Tier II Human 3349 Genes GS235245: [MeSH] Endocytosis : D004705
Expand Tier III Rat 398 Genes GS224137: Anxiety related response QTL 11 (Anxrr11 Published QTL Chr 18)
Expand Tier III Rat 403 Genes GS224330: Insulin dependent diabetes mellitus QTL 4 (Iddm4 Published QTL Chr 18)
Expand Tier II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier II Human 404 Genes GS242283: [MeSH] Myelin Sheath : D009186
Expand Tier II Human 9707 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Mouse GO 9 Genes GS190433: GO:0043217 myelin maintenance
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 II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Mouse GO 123 Genes GS187753: GO:0019228 regulation of action potential in neuron
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 168 Genes GS236784: [MeSH] Polyneuropathies : D011115
Expand Human 123 Genes GS222118: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Mouse 201 Genes GS135963: HDL QTL 31 (Hdlq31, Published QTL Chr 18)
Expand Tier I Human GO 27 Genes GS199684: GO:0014037 Schwann cell differentiation
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Mouse 200 Genes GS229762: MSigDB Geneset - GSE20366_TREG_VS_NAIVE_CD4_TCELL_DEC205_CONVERSION_UP
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 2 Genes GS176173: HP:0003400 Basal lamina 'onion bulb' formation
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Mouse 289 Genes GS136387: ocular degeneration with sex reversal modifier 1 (Odsm1, Published QTL Chr 18)
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier II Human 2219 Genes GS238955: [MeSH] Protein Interaction Domains and Motifs : D054730
Expand Tier I Mouse 268 Genes GS135982: wound healing/regeneration 9 (Heal9, Published QTL Chr 18)
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier III Rat 147 Genes GS223733: Renal function QTL 26 (Rf26 Published QTL Chr 18)
Expand Tier I Human GO 559 Genes GS208092: GO:0005768 endosome
Expand Tier I Mouse GO 296 Genes GS177347: GO:0042391 regulation of membrane potential
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 79 Genes GS197803: GO:0007422 peripheral nervous system development
Expand Tier III Rat 656 Genes GS223687: Blood pressure QTL 232 (Bp232 Published QTL Chr 18)
Expand Tier I Mouse GO 24 Genes GS182883: GO:0014037 Schwann cell differentiation
Expand Tier I Mouse 208 Genes GS136409: organ weight QTL 9 (Orgwq9, Published QTL Chr 18)
Expand Tier I Mouse GO 606 Genes GS184506: GO:0006873 cellular ion homeostasis
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier III Rat 153 Genes GS223282: Blood pressure QTL 352 (Bp352 Published QTL Chr 18)
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse 241 Genes GS135726: duration of locomotor activity 2 (Dloc2, Published QTL Chr 18)
Expand Tier I Human 44 Genes GS174918: HP:0000764 Peripheral axonal degeneration
Expand Tier I Human 372 Genes GS228709: MSigDB Geneset - WGGAATGY_V$TEF1_Q6
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
Expand Tier I Mouse 239 Genes GS136491: proteoglycan induced arthritis 11 (Pgia11, Published QTL Chr 18)
Expand Tier I Mouse GO 58 Genes GS189481: GO:0055037 recycling endosome
Expand Tier I Human GO 166 Genes GS194334: GO:0042063 gliogenesis
Expand Tier I Mouse 442 Genes GS136565: radiation pulmonary fibrosis 4 (Radpf4, Published QTL Chr 18)
Expand Tier I Mouse MP 212 Genes GS169362: MP:0000920 abnormal myelination
Expand Tier I Human 238 Genes GS232281: PC Geneset - "V$LMO2COM_02" pathway genes
Expand Tier I Human 1187 Genes GS232363: PC Geneset - "CTTTGA_V$LEF1_Q2" pathway genes
Expand Tier II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 128 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier III Rat 422 Genes GS223379: Bone mineral density QTL 66 (Bmd66 Published QTL Chr 18)
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse GO 100 Genes GS189593: GO:0042552 myelination
Expand Tier I Mouse 439 Genes GS135602: circulating hormone level QTL 10 (Chlq10, Published QTL Chr 18)
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 8 Genes GS174434: HP:0007107 Segmental peripheral demyelination
Expand Tier II Human 128 Genes GS233961: [MeSH] Hereditary Sensory and Motor Neuropathy : D015417
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier III Rat 464 Genes GS224159: Mammary tumor resistance QTL 8 (Mamtr8 Published QTL Chr 18)
Expand Tier III Rat 397 Genes GS224082: Body weight QTL 157 (Bw157 Published QTL Chr 18)
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human GO 736 Genes GS204608: GO:0019226 transmission of nerve impulse
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Mouse MP 76 Genes GS167104: MP:0005403 abnormal nerve conduction
Expand Tier III Rat 269 Genes GS223946: Blood pressure QTL 47 (Bp47 Published QTL Chr 18)
Expand Tier I Mouse 391 Genes GS135521: body weight at necropsy 5 (Bwtn5, Published QTL Chr 18)
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Mouse MP 47 Genes GS167939: MP:0008814 reduced nerve conduction velocity
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier II Human 9232 Genes GS245445: [MeSH] Stem Cells : D013234
Expand Tier III Rat 251 Genes GS223319: Blood pressure QTL 228 (Bp228 Published QTL Chr 18)
Expand Tier I Human 227 Genes GS227775: MSigDB Geneset - SYATTGTG_UNKNOWN
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 33 Genes GS229479: MSigDB Geneset - chr5q32
Expand Tier I Human 687 Genes GS227437: MSigDB Geneset - YTATTTTNR_V$MEF2_02
Expand Tier I Human 46 Genes GS171759: HP:0002936 Distal sensory impairment
Expand Tier III Rat 361 Genes GS223587: Body weight QTL 165 (Bw165 Published QTL Chr 18)
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Mouse 391 Genes GS136713: susceptibility to lung cancer 14 (Sluc14, Published QTL Chr 18)
Expand Tier I Human GO 80 Genes GS206464: GO:0042552 myelination
Expand Tier I Human 937 Genes GS230176: MSigDB Geneset - TTANTCA_UNKNOWN
Expand Tier I Mouse GO 5221 Genes GS179211: GO:0007154 cell communication
Expand Tier I Mouse 249 Genes GS136435: pulmonary adenoma susceptibility 7 (Pas7, Published QTL Chr 18)
Expand Tier I Mouse GO 160 Genes GS177596: GO:0042063 gliogenesis
Expand Tier II Human 4765 Genes GS236201: [MeSH] Embryonic Stem Cells : D053595
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Human 123 Genes GS219579: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_FACTORS_INVOLVED_IN_MEGAKARYOCYTE_DEVELOPMENT_AND_PLATELET_PRODUCTION
Expand Tier I Mouse MP 569 Genes GS166743: MP:0002229 neurodegeneration
Expand Tier II Human 13620 Genes GS234949: [MeSH] Genetic Vectors : D005822
Expand Tier I Human 7 Genes GS173684: HP:0003387 Decreased number of large peripheral myelinated nerve fibers
Expand Tier II Mouse 122 Genes GS35318: Neocortex Gene expression correlates of Acoustic Startle Response Percentage of maximum response at 85 db in Males BXD
Expand Tier I Mouse 400 Genes GS136156: limb length QTL 6 (Lmblgq6, Published QTL Chr 18)
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 1235 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier III Rat 554 Genes GS224779: Insulin dependent diabetes mellitus QTL 35 (Iddm35 Published QTL Chr 18)
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier II Human 8519 Genes GS243346: [MeSH] Chromosomes, Human : D002877
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
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 II Human 32928 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier I Mouse 248 Genes GS136102: lupus NZB x NZW 6 (Lbw6, Published QTL Chr 18)
Expand Tier I Mouse DRG 678 Genes provisional GS87011: Table S2: List of Cocaine-Treated HDAC5 KO vs. Cocaine-Treated WT Significantly Regulated Genes. [DRG]
Expand Tier I Human GO 6743 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier II Human 13292 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Mouse GO 16 Genes GS191605: GO:0032292 peripheral nervous system axon ensheathment
Expand Tier I Mouse 420 Genes GS136017: heart failure modifier 4 (Hrtfm4, Published QTL Chr 18)
Expand Tier II Human 3010 Genes GS241608: [MeSH] Haplotypes : D006239
Expand Tier III Rat 103 Genes GS224564: Serum cholesterol level QTL 27 (Scl27 Published QTL Chr 18)
Expand Tier I Human GO 1691 Genes GS209960: GO:0003008 system process
Expand Tier III Rat 401 Genes GS224510: Body weight QTL 11 (Bw11 Published QTL Chr 18)
Expand Tier I Mouse MP 854 Genes GS168958: MP:0003492 abnormal involuntary movement
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human 25 Genes GS171767: HP:0003431 Decreased motor nerve conduction velocity
Expand Tier I Human GO 17 Genes GS210069: GO:0022011 myelination in peripheral nervous system
Expand Tier II Human 56931 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier II Human 30254 Genes GS243763: [MeSH] Intracellular Space : D042541
Expand Tier III Rat 283 Genes GS223444: Blood pressure QTL 237 (Bp237 Published QTL Chr 18)
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 27 Genes GS176587: HP:0001271 Polyneuropathy
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier III Rat 153 Genes GS223480: Mammary carcinoma susceptibility QTL 22 (Mcs22 Published QTL Chr 18)
Expand Tier I Mouse 456 Genes GS136197: lung squamous cell carcinoma 3 (Lscc3, Published QTL Chr 18)
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 7 Genes GS196057: GO:0032287 peripheral nervous system myelin maintenance
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier III Rat 155 Genes GS224028: Bone mineral density QTL 23 (Bmd23 Published QTL Chr 18)
Expand Tier II Human 73218 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Mouse MP 435 Genes GS170131: MP:0008415 abnormal neurite morphology
Expand Tier III Rat 252 Genes GS223711: Prepulse inhibition QTL 2 (Ppulsi2 Published QTL Chr 18)
Expand Tier I Mouse 391 Genes GS136199: lung tumor shape-determining 1 (Ltsd1, Published QTL Chr 18)
Expand Tier III Rat 468 Genes GS224072: Bone structure and strength QTL 85 (Bss85 Published QTL Chr 18)
Expand Tier I Mouse 441 Genes GS135940: HDL level 40 (Hdl40, Published QTL Chr 18)
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier II Human 716 Genes GS238880: [MeSH] Chromosomes, Human, 4-5 : D002905
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 710 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier II Human 35136 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Mouse 99 Genes GS129141: insulin dependent diabetes susceptibility 21.2 (Idd21.2 Published QTL Chr 18)
Expand Tier I Human 8 Genes GS175374: HP:0010546 Muscle fibrillation
Expand Tier III Rat 485 Genes GS223863: Stress Responsive Adrenal Weight QTL 6 (Sradr6 Published QTL Chr 18)
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier II Human 11662 Genes GS239443: [MeSH] RNA Splicing : D012326
Expand Tier I Mouse 239 Genes GS135306: angiogenesis due to FGF2 QTL 4 (Angfq4, Published QTL Chr 18)
Expand Tier II Human 22746 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier III Rat 350 Genes GS223997: Glucose level QTL 55 (Gluco55 Published QTL Chr 18)
Expand Tier I Human 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier II Human 6195 Genes GS243775: [MeSH] Genetic Predisposition to Disease : D020022
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier II Human 9287 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse 437 Genes GS136268: "macronutrient intake, fat 2" (Mnif2, Published QTL Chr 18)
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4073 Genes GS180034: GO:0032502 developmental process
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 2753 Genes GS241422: [MeSH] Nerve Fibers : D009412
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
Expand Tier II Human 457 Genes GS234238: [MeSH] Nerve Fibers, Myelinated : D009413
Expand Tier III Rat 698 Genes GS223146: Bone structure and strength QTL 20 (Bss20 Published QTL Chr 18)
Expand Tier II Mouse 243 Genes GS83969: cocaine induced activation 14 (Cocia14, Published QTL, Chr 18)
Expand Tier I Mouse 267 Genes GS136423: pulmonary adenoma resistance 2 (Par2, Published QTL Chr 18)
Expand Tier I Mouse 458 Genes GS135810: experimental severe malaria resistance (Esmr, Published QTL Chr 18)
Expand Tier I Human 1209 Genes GS230549: MSigDB Geneset - CTTTGA_V$LEF1_Q2
Expand Tier I Human 1 Genes GS176284: HP:0009831 Mononeuropathy
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human GO 136 Genes GS201741: GO:0001508 regulation of action potential
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Mouse MP 3 Genes GS164279: MP:0010732 abnormal node of Ranvier morphology
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Mouse GO 7 Genes GS179287: GO:0032287 peripheral nervous system myelin maintenance
Expand Tier III Rat 665 Genes GS224163: Mammary tumor resistance QTL 6 (Mamtr6 Published QTL Chr 18)
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 II Human 12489 Genes GS241292: [MeSH] Pathological Conditions, Signs and Symptoms : D013568
Expand Tier I Human GO 585 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Human 471 Genes GS222221: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_HEMOSTASIS
Expand Tier I Mouse 208 Genes GS135922: growth traits 7 (Gwth7, Published QTL Chr 18)
Expand Tier II Human 12369 Genes GS245348: [MeSH] RNA Processing, Post-Transcriptional : D012323
Expand Tier II Human 15964 Genes GS237339: [MeSH] Regulatory Sequences, Nucleic Acid : D012045
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier III Rat 533 Genes GS224826: Bone structure and strength QTL 46 (Bss46 Published QTL Chr 18)
Expand Tier II Human 657 Genes GS244062: [MeSH] Oligodendroglia : D009836