Gene Details



Hs.655974 and homologs in 7 species are found in 737 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 II Mouse 161 Genes GS35309: Whole Brain Gene expression correlates of Acoustic Startle Response Percentage of maximum startle response at 80 db in Females & Males BXD
Expand Tier II Human 37 Genes GS242563: [MeSH] Fundus Oculi : D005654
Expand Tier I Mouse MP 1698 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier II Human 350 Genes GS236887: [MeSH] Ear Diseases : D004427
Expand Tier II Human 1017 Genes GS237944: [MeSH] Chromosomes, Human, Pair 1 : D002878
Expand Tier II Human 6358 Genes GS238474: [MeSH] Hormones : D006728
Expand Tier I Mouse MP 279 Genes GS163596: MP:0000026 abnormal inner ear morphology
Expand Tier II Human 187 Genes GS236163: [MeSH] Deafness : D003638
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 Human 49 Genes GS221924: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Chinese probands
Expand Tier I Human GO 224 Genes GS210290: GO:0016324 apical plasma membrane
Expand Tier I Mouse GO 3706 Genes GS188641: GO:0071944 cell periphery
Expand Tier I Mouse 465 Genes GS136446: pentobarbital withdrawal QTL 1 (Pbw1, Published QTL Chr 1)
Expand Tier II Human 10505 Genes GS238504: [MeSH] Tissues : D014024
Expand Tier II Human 452 Genes GS234388: [MeSH] Perception : D010465
Expand Tier II Human 5416 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier II Human 700 Genes GS235429: [MeSH] Ear : D004423
Expand Tier II Human 1225 Genes GS242407: [MeSH] Mental Processes : D008606
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human 190 Genes GS227366: MSigDB Geneset - GSE8515_CTRL_VS_IL6_4H_STIM_MAC_DN
Expand Tier II Human 390 Genes GS245136: [MeSH] Frameshift Mutation : D016368
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 178 Genes GS230238: MSigDB Geneset - GSE17974_0H_VS_0.5H_IN_VITRO_ACT_CD4_TCELL_DN
Expand Tier I Mouse MP 388 Genes GS170108: MP:0003727 abnormal retinal layer morphology
Expand Tier I Mouse 465 Genes GS136573: radiation-induced acute myeloid leukemia sensitivity 1 (Ramls1, Published QTL Chr 1)
Expand Tier I Mouse GO 454 Genes GS181012: GO:0007423 sensory organ development
Expand Tier I Mouse 385 Genes GS135862: femur breaking strength 5 (Fembrs5, Published QTL Chr 1)
Expand Tier III Rat 367 Genes GS224153: Glucose level QTL 63 (Gluco63 Published QTL Chr 13)
Expand Tier I Mouse MP 182 Genes GS163581: MP:0001004 abnormal retinal photoreceptor morphology
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 I Mouse 385 Genes GS135953: HDL QTL 20 (Hdlq20, Published QTL Chr 1)
Expand Tier I Mouse MP 190 Genes GS166394: MP:0003728 abnormal retinal photoreceptor layer morphology
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 I Mouse 465 Genes GS135270: alcohol dependency 1 (Alcdp1, Published QTL Chr 1)
Expand Tier I Mouse 454 Genes GS135788: ethanol induced locomotor activity 1 (Eila1, Published QTL Chr 1)
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse GO 123 Genes GS193046: GO:0050953 sensory perception of light stimulus
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 10433 Genes GS239764: [MeSH] Glycoproteins : D006023
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 II Human 745 Genes GS238514: [MeSH] Otorhinolaryngologic Diseases : D010038
Expand Tier I Mouse GO 1 Genes GS188339: GO:0060171 stereocilium membrane
Expand Tier I Mouse MP 49 Genes GS166022: MP:0004408 decreased cochlear hair cell number
Expand Tier I Human GO 124 Genes GS210482: GO:0007605 sensory perception of sound
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier II Human 1485 Genes GS240465: [MeSH] Polymorphism, Restriction Fragment Length : D012150
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Mouse MP 47 Genes GS164793: MP:0008587 short photoreceptor outer segment
Expand Tier I Human 188 Genes GS229515: MSigDB Geneset - IL2_UP.V1_UP
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier II Human 1090 Genes GS238558: [MeSH] Tandem Repeat Sequences : D020080
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier II Mouse 435 Genes GS83986: cocaine related behavior 2 (Cocrb2, Published QTL, Chr 1)
Expand Tier II Mouse 399 Genes GS84113: differences in cocaine responsiveness (Published QTL, Chr 1)
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 121 Genes GS200823: GO:0009913 epidermal cell differentiation
Expand Tier II Human 3455 Genes GS239907: [MeSH] Cell Surface Extensions : D022081
Expand Tier II Human 30225 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Mouse 460 Genes GS135464: blood pressure QTL 21 (Bpq21, Published QTL Chr 1)
Expand Tier II Human 14581 Genes GS241611: [MeSH] Organic Chemistry Processes : D055602
Expand Tier II Human 2100 Genes GS239241: [MeSH] Eye Proteins : D005136
Expand Tier I Mouse MP 228 Genes GS163320: MP:0000031 abnormal cochlea morphology
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier II Human 2536 Genes GS240585: [MeSH] Sensory Receptor Cells : D011984
Expand Tier I Mouse GO 187 Genes GS187229: GO:0043583 ear development
Expand Tier I Mouse MP 2893 Genes GS165466: MP:0003632 abnormal nervous system morphology
Expand Tier II Human 5149 Genes GS237067: [MeSH] Contractile Proteins : D003285
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human GO 4 Genes GS198531: GO:0002139 stereocilia coupling link
Expand Tier II Human 432 Genes GS236659: [MeSH] Codon, Terminator : D018388
Expand Tier I Human 12 Genes GS171801: HP:0008527 Congenital sensorineural hearing impairment
Expand Tier I Mouse GO 28 Genes GS181577: GO:0017022 myosin binding
Expand Tier I Human GO 2 Genes GS205196: GO:0060171 stereocilium membrane
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier II Mouse 399 Genes GS84111: differences in cocaine responsiveness (Published QTL, Chr 1)
Expand Tier I Human 136 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier II Human 2140 Genes GS234970: [MeSH] Genetic Loci : D056426
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 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 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 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 Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Mouse MP 187 Genes GS168193: MP:0000966 decreased sensory neuron number
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human 16 Genes GS175180: HP:0011073 Abnormality of dental color
Expand Tier I Mouse MP 171 Genes GS168066: MP:0002622 abnormal cochlear hair cell morphology
Expand Tier II Mouse 27 Genes GS35554: Neocortex Gene expression correlates of Morphine photocell counts minutes 120-135 in Males BXD
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier I Human GO 1006 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Human 167 Genes GS222318: Coding region point mutations in ASD probands.
Expand Tier II Human 9858 Genes GS242870: [MeSH] Polymorphism, Genetic : D011110
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier II Human 701 Genes GS237186: [MeSH] Chemically-Induced Disorders : D064419
Expand Tier I Mouse MP 95 Genes GS166313: MP:0008450 retinal photoreceptor degeneration
Expand Tier II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier II Human 21236 Genes GS240239: [MeSH] Sequence Homology : D017385
Expand Tier II Human 4782 Genes GS239103: [MeSH] Serum Globulins : D012712
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 136 Genes GS241401: [MeSH] Tobacco Use Cessation : D020340
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Human 70 Genes GS222261: Genes associated with retinitis pigmentosa (RP) on OMIM database
Expand Tier II Human 2845 Genes GS244436: [MeSH] Gene Frequency : D005787
Expand Tier I Human GO 38 Genes GS198664: GO:0043954 cellular component maintenance
Expand Tier II Human 4022 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier II Human 352 Genes GS238427: [MeSH] Neuroepithelial Cells : D046569
Expand Tier I Human GO 493 Genes GS209225: GO:0007600 sensory perception
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier I Mouse 295 Genes GS136536: promotion susceptibility QTL 3 (Psl3, Published QTL Chr 1)
Expand Tier I Mouse 460 Genes GS136188: lipoprotein QTL 3 (Lprq3, Published QTL Chr 1)
Expand Tier II Human 9151 Genes GS238044: [MeSH] Acid Anhydride Hydrolases : D017766
Expand Tier II Human 497 Genes GS244503: [MeSH] Mechanoreceptors : D008465
Expand Human 70 Genes GS221898: RetNet genes linked to retinitis pigmentosa (RP)
Expand Tier II Mouse 366 Genes GS84115: morphine preference (Published QTL, Chr 1)
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 5 Genes GS194007: GO:0048496 maintenance of organ identity
Expand Tier I Human 49 Genes GS173812: HP:0000738 Hallucinations
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier II Human 6887 Genes GS234190: [MeSH] Polymers : D011108
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier II Mouse 161 Genes GS35289: Whole Brain Gene expression correlates of Prepulse inhibition at 80db in Females & Males BXD
Expand Tier I Mouse 325 Genes GS136699: systematic lupus erythematosus susceptibility 1c (Sle1c, Published QTL Chr 1)
Expand Tier II Human 7085 Genes GS244254: [MeSH] Antigens, Surface : D000954
Expand Tier I Human GO 6 Genes GS205287: GO:0035315 hair cell differentiation
Expand Tier II Human 5493 Genes GS240446: [MeSH] Pharmacokinetics : D010599
Expand Tier I Mouse MP 323 Genes GS163432: MP:0006069 abnormal retinal neuronal layer morphology
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
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 II Human 2776 Genes GS237733: [MeSH] Mental Disorders : D001523
Expand Tier II Human 4510 Genes GS241347: [MeSH] Microfilament Proteins : D008840
Expand Tier I Mouse MP 178 Genes GS163068: MP:0000045 abnormal hair cell morphology
Expand Tier II Human 15116 Genes GS243569: [MeSH] Macromolecular Substances : D046911
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
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 Mouse 466 Genes GS136839: trypansomiasis infection response 3c (Tir3c, Published QTL Chr 1)
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 199 Genes GS230527: MSigDB Geneset - GSE360_L_DONOVANI_VS_B_MALAYI_HIGH_DOSE_DC_UP
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Mouse MP 32 Genes GS168863: MP:0004402 decreased cochlear outer hair cell number
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier II Human 26 Genes GS237994: [MeSH] Deaf-Blind Disorders : D054062
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 244 Genes GS179362: GO:0005929 cilium
Expand Tier II Human 700 Genes GS238897: [MeSH] Sociology : D012961
Expand Tier I Mouse GO 377 Genes GS179537: GO:0031012 extracellular matrix
Expand Tier II Human 5111 Genes GS242217: [MeSH] Muscle Proteins : D009124
Expand Tier I Mouse 454 Genes GS136703: systematic lupus erythematosus susceptibility 9 (Sle9, Published QTL Chr 1)
Expand Tier II Human 218 Genes GS239225: [MeSH] Nicotine : D009538
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Human GO 3116 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier II Human 2632 Genes GS242312: [MeSH] Extracellular Matrix Proteins : D016326
Expand Tier II Human 6955 Genes GS245398: [MeSH] Protein Isoforms : D020033
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 849 Genes GS236202: [MeSH] Microsatellite Repeats : D018895
Expand Tier II Human 14624 Genes GS236362: [MeSH] Organic Chemistry Phenomena : D055601
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Human 74 Genes GS222884: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier II Human 640 Genes GS237443: [MeSH] Ear, Inner : D007758
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier II Human 15724 Genes GS239132: [MeSH] Gene Expression Regulation, Developmental : D018507
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier II Human 61 Genes GS238726: [MeSH] Blindness : D001766
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 Mouse 454 Genes GS136969: Y-linked autoimmune acceleration 4 (Yaa4, Published QTL Chr 1)
Expand Tier I Mouse GO 293 Genes GS192775: GO:0045177 apical part of cell
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Mouse GO 441 Genes GS180207: GO:0045596 negative regulation of cell differentiation
Expand Tier I Human 248 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Mouse 454 Genes GS135994: hippocampal weight 1 (Hipp1, Published QTL Chr 1)
Expand Tier I Human GO 634 Genes GS194613: GO:0008092 cytoskeletal protein binding
Expand Tier II Mouse 399 Genes GS84112: differences in cocaine responsiveness (Published QTL, Chr 1)
Expand Tier I Mouse MP 959 Genes GS166244: MP:0002752 abnormal somatic nervous system morphology
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier I Human GO 9088 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 280 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human GO 186 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier I Human GO 535 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Human 140 Genes GS229946: MSigDB Geneset - KRAS.BREAST_UP.V1_UP
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 465 Genes GS135552: CD8 T memory cell subset 1 (Cd8mts1, Published QTL Chr 1)
Expand Tier I Mouse GO 605 Genes GS177870: GO:0008092 cytoskeletal protein binding
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier II Human 7284 Genes GS236354: [MeSH] Gene Deletion : D017353
Expand Tier I Mouse 431 Genes GS135596: cholesterol and HDL QTL 1 (Chldq1, Published QTL Chr 1)
Expand Tier II Human 9312 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier I Mouse 465 Genes GS135344: atherosclerosis 9 (Ath9, Published QTL Chr 1)
Expand Tier III Human 1 Genes GS221923: Multiplex ligation-dependent probe amplification (MLPA) and array-based comparative genomic hybridization (aCGH) used to study mutations in USH2A gene that cause retinitis pigmentosa (RP)
Expand Tier II Human 10296 Genes GS240252: [MeSH] Intercellular Signaling Peptides and Proteins : D036341
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Mouse MP 51 Genes GS165924: MP:0004400 abnormal cochlear outer hair cell number
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier II Human 23706 Genes GS235056: [MeSH] Peptides : D010455
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier II Human 3773 Genes GS234965: [MeSH] Cell Adhesion Molecules : D015815
Expand Tier I Human 198 Genes GS229405: MSigDB Geneset - GSE360_L_DONOVANI_VS_T_GONDII_MAC_UP
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Mouse MP 3522 Genes GS163803: MP:0003631 nervous system phenotype
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human GO 39 Genes GS202686: GO:0060113 inner ear receptor cell differentiation
Expand Tier I Human 190 Genes GS230318: MSigDB Geneset - GSE13411_NAIVE_VS_IGM_MEMORY_BCELL_UP
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 52 Genes GS167572: MP:0001006 abnormal retinal cone cell morphology
Expand Tier I Mouse GO 24 Genes GS186963: GO:0045494 photoreceptor cell maintenance
Expand Tier I Human 200 Genes GS229143: MSigDB Geneset - GSE360_L_DONOVANI_VS_L_MAJOR_DC_UP
Expand Tier I Mouse 330 Genes GS136796: total body bone mineral density 1 (Tbbmd1, Published QTL Chr 1)
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier I Human GO 185 Genes GS196034: GO:0031253 cell projection membrane
Expand Tier II Human 3004 Genes GS240265: [MeSH] Neurons, Afferent : D009475
Expand Tier I Human 361 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier II Mouse 93 Genes GS34767: Whole Brain Gene expression correlates of Novel environment vertical activity counts minutes 45-60 in Females & Males BXD
Expand Tier I Mouse GO 10879 Genes GS181473: GO:0005488 binding
Expand Human 14 Genes GS221900: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Italian probands
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 825 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier II Human 13521 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Mouse 449 Genes GS136475: plasma cholesterol 1 (Pcho1, Published QTL Chr 1)
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier II Mouse 435 Genes GS84108: cocaine related behavior Chr1 at D1Ncvs12 (Published QTL)
Expand Tier I Mouse 434 Genes GS135508: body weight at 8 weeks QTL 1 (Bw8q1, Published QTL Chr 1)
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 68 Genes GS204815: GO:0005902 microvillus
Expand Tier I Human 78 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Mouse 465 Genes GS135601: circulating hormone level QTL 1 (Chlq1, Published QTL Chr 1)
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 Mouse 465 Genes GS136863: triglycerides (Trglyd, Published QTL Chr 1)
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 58105 Genes GS242107: [MeSH] Chemical Processes : D055599
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 II Mouse 443 Genes GS84110: Acute ethanol sensitivity on Chr1 (Published QTL)
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Mouse GO 609 Genes GS185024: GO:0044463 cell projection part
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Mouse GO 1041 Genes GS184451: GO:0044421 extracellular region part
Expand Tier I Mouse 377 Genes GS136613: colon tumor susceptibility 3 (Scc3, Published QTL Chr 1)
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Mouse MP 487 Genes GS166123: MP:0002102 abnormal ear morphology
Expand Tier II Human 5853 Genes GS241597: [MeSH] Disease Models, Animal : D004195
Expand Tier I Mouse GO 1825 Genes GS193270: GO:0005576 extracellular region
Expand Tier I Mouse GO 2138 Genes GS186067: GO:0050877 neurological system process
Expand Tier II Human 8645 Genes GS234354: [MeSH] Cytoskeletal Proteins : D003598
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Mouse MP 16 Genes GS167659: MP:0008444 retinal cone cell degeneration
Expand Tier II Human 3244 Genes GS240069: [MeSH] Microtubule Proteins : D008868
Expand Tier I Mouse MP 459 Genes GS163138: MP:0005253 abnormal eye physiology
Expand Tier II Human 839 Genes GS238687: [MeSH] Disease : D004194
Expand Tier I Mouse GO 2498 Genes GS193018: GO:0003008 system process
Expand Tier II Human 393 Genes GS239233: [MeSH] Codon, Nonsense : D018389
Expand Tier II Human 821 Genes GS235519: [MeSH] Syndrome : D013577
Expand Tier I Mouse MP 71 Genes GS165854: MP:0004406 abnormal cochlear hair cell number
Expand Tier II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier II Human 1434 Genes GS240994: [MeSH] Alkaloids : D000470
Expand Tier I Human GO 636 Genes GS201839: GO:0044463 cell projection part
Expand Tier II Human 625 Genes GS243813: [MeSH] Family : D005190
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
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 II Human 11815 Genes GS238961: [MeSH] Nerve Tissue Proteins : D009419
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 II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Human 74 Genes GS221014: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier I Mouse 465 Genes GS136467: pentobarbital withdrawal modifier (Pbwm, Published QTL Chr 1)
Expand Tier I Mouse 467 Genes GS136729: susceptibility to lung cancer 5 (Sluc5, Published QTL Chr 1)
Expand Tier I Human 42 Genes GS227948: MSigDB Geneset - chr1q41
Expand Human 74 Genes GS219653: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PEROXISOME
Expand Tier I Mouse MP 51 Genes GS168880: MP:0004736 abnormal distortion product otoacoustic emission
Expand Tier III Rat 555 Genes GS223271: Bone structure and strength QTL 34 (Bss34 Published QTL Chr 13)
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier II Human 3385 Genes GS237069: [MeSH] Congenital Abnormalities : D000013
Expand Tier I Mouse GO 41 Genes GS184631: GO:0005518 collagen binding
Expand Tier I Mouse MP 223 Genes GS169032: MP:0005551 abnormal eye electrophysiology
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 88 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier II Human 2272 Genes GS239652: [MeSH] Genes, Recessive : D005808
Expand Tier II Human 161 Genes GS238585: [MeSH] Retinitis Pigmentosa : D012174
Expand Tier II Human 73996 Genes GS244482: [MeSH] Nucleic Acids, Nucleotides, and Nucleosides : D009706
Expand Tier I Mouse 467 Genes GS136594: rotarod performance 1 (Rrodp1, Published QTL Chr 1)
Expand Tier I Mouse GO 65 Genes GS187955: GO:0005902 microvillus
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 102 Genes GS178598: GO:0072372 primary cilium
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse 199 Genes GS228998: MSigDB Geneset - GSE17721_PAM3CSK4_VS_GADIQUIMOD_4H_BMDM_UP
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 369 Genes GS84114: activity response to ethanol (Published QTL, Chr 1)
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier I Mouse 465 Genes GS135867: fasting glucose 2 (Fglu2, Published QTL Chr 1)
Expand Tier II Human 109 Genes GS237886: [MeSH] Vision Disorders : D014786
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier II Human 321 Genes GS244736: [MeSH] Solanaceous Alkaloids : D012991
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Human 492 Genes GS222864: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS
Expand Tier I Mouse 460 Genes GS136692: systemic lupus erythmatosus susceptibility 1 (Sle1, Published QTL Chr 1)
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Mouse GO 133 Genes GS193043: GO:0050954 sensory perception of mechanical stimulus
Expand Tier I Mouse 906 Genes GS129103: bone mineral density 5 (Bmd5 Published QTL Chr 1)
Expand Tier I Mouse 454 Genes GS136740: spermatocyte heat stress resistance 1 (Sphsr1, Published QTL Chr 1)
Expand Tier II Human 3263 Genes GS237180: [MeSH] Genetic Markers : D005819
Expand Tier II Human 1026 Genes GS246010: [MeSH] Codon : D003062
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Mouse 465 Genes GS135673: cholesterol QTL 2 (Cq2, Published QTL Chr 1)
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
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 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Mouse 454 Genes GS136381: obesity QTL 9 (Obq9, Published QTL Chr 1)
Expand Tier I Mouse 460 Genes GS135583: chronic glomerulonephritis in NZM 1 (Cgnz1, Published QTL Chr 1)
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier II Human 612 Genes GS243116: [MeSH] Laminin : D007797
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Human 198 Genes GS227900: MSigDB Geneset - GSE8515_CTRL_VS_IL1_4H_STIM_MAC_UP
Expand Tier II Human 1896 Genes GS237199: [MeSH] Chromosomes, Human, 1-3 : D002900
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier II Human 136 Genes GS240776: [MeSH] Smoking Cessation : D016540
Expand Tier I Mouse GO 553 Genes GS188475: GO:0051093 negative regulation of developmental process
Expand Tier I Mouse GO 28 Genes GS181643: GO:0032421 stereocilium bundle
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier II Human 3012 Genes GS234181: [MeSH] Retina : D012160
Expand Tier III Rat 922 Genes GS223612: Blood pressure QTL 244 (Bp244 Published QTL Chr 13)
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier II Human 987 Genes GS243019: [MeSH] Tobacco Use : D064424
Expand Tier I Mouse GO 213 Genes GS193348: GO:0016324 apical plasma membrane
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 90 Genes GS208328: GO:0005604 basement membrane
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier I Mouse GO 94 Genes GS191405: GO:0005604 basement membrane
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse MP 142 Genes GS169847: MP:0004399 abnormal cochlear outer hair cell morphology
Expand Tier II Human 10298 Genes GS238960: [MeSH] Membrane Glycoproteins : D008562
Expand Tier I Mouse GO 37 Genes GS181873: GO:0043954 cellular component maintenance
Expand Tier I Mouse MP 702 Genes GS167922: MP:0000959 abnormal somatic sensory system morphology
Expand Tier II Human 2555 Genes GS242366: [MeSH] Inheritance Patterns : D040582
Expand Tier I Mouse GO 23 Genes GS187859: GO:0032391 photoreceptor connecting cilium
Expand Tier I Human GO 132 Genes GS209984: GO:0050954 sensory perception of mechanical stimulus
Expand Tier II Human 9707 Genes GS235744: [MeSH] Neurons : D009474
Expand Tier I Mouse MP 433 Genes GS165390: MP:0003224 neuron degeneration
Expand Tier II Human 6187 Genes GS243844: [MeSH] Receptors, G-Protein-Coupled : D043562
Expand Tier II Human 4906 Genes GS239789: [MeSH] Adenosine Triphosphatases : D000251
Expand Tier II Human 650 Genes GS243363: [MeSH] Polymorphism, Single-Stranded Conformational : D018807
Expand Tier I Human CTD 1151 Genes GS121437: Fluorouracil interacting genes (MeSH:D005472) in CTD
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human GO 23 Genes GS198432: GO:0032420 stereocilium
Expand Tier I Mouse 466 Genes GS135476: bone response to mechanical loading 1 (Brml1, Published QTL Chr 1)
Expand Tier I Mouse 458 Genes GS136698: systematic lupus erythematosus susceptibility 1b (Sle1b, Published QTL Chr 1)
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Mouse 465 Genes GS135501: basal locomotor activity 4 (Bslm4, Published QTL Chr 1)
Expand Tier III Rat 381 Genes GS223355: Glomerulus QTL 15 (Glom15 Published QTL Chr 13)
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier I Mouse GO 141 Genes GS179265: GO:0031253 cell projection membrane
Expand Tier II Human 23476 Genes GS237836: [MeSH] Carrier Proteins : D002352
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier II Human 2037 Genes GS237303: [MeSH] Mutation, Missense : D020125
Expand Tier I Mouse 467 Genes GS135683: Ctla4 expression QTL (Ctex, Published QTL Chr 1)
Expand Tier II Human 16221 Genes GS239275: [MeSH] Intracellular Signaling Peptides and Proteins : D047908
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier II Human 289 Genes GS243183: [MeSH] Hearing Loss : D034381
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier II Mouse 151 Genes GS34251: Striatum Gene expression correlates of Activity in altered context during presentation of cue in Males BXD
Expand Tier I Mouse GO 119 Genes GS193537: GO:0007605 sensory perception of sound
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse 104 Genes GS129202: zinc induced tolerance 1 (Zit1 Published QTL Chr 1)
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 482 Genes GS235047: [MeSH] Retinal Degeneration : D012162
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Human 62 Genes GS221933: Mutations of 60 known causative genes in 157 families with retinitis pigmentosa (RP) based on exome sequencing
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 538 Genes GS223607: Blood pressure QTL 241 (Bp241 Published QTL Chr 13)
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Mouse GO 4 Genes GS182628: GO:0002142 stereocilia ankle link complex
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier II Human 3301 Genes GS241289: [MeSH] Behavior : D001519
Expand Tier II Mouse 324 Genes GS84116: ethanol withdrawal on Chr1 at Xmv41 (Published QTL)
Expand Tier I Mouse GO 3605 Genes GS190682: GO:0007275 multicellular organismal development
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 GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier II Mouse 85 Genes GS34574: Striatum Gene expression correlates of Novel environment distance (cm) travelled minutes 0-15 in Males BXD
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier II Human 1528 Genes GS242356: [MeSH] Photoreceptor Cells : D010786
Expand Tier III Rat 894 Genes GS223393: Experimental allergic encephalomyelitis QTL 17 (Eae17 Published QTL Chr 13)
Expand Tier II Mouse 187 Genes GS84118: ethanol induced locomotion (Published QTL, Chr 1)
Expand Tier I Mouse 465 Genes GS135799: escape latencies during navigation task (Elnt, Published QTL Chr 1)
Expand Tier I Mouse 430 Genes GS135968: HDL QTL 5 (Hdlq5, Published QTL Chr 1)
Expand Tier II Human 1846 Genes GS242116: [MeSH] Retinal Neurons : D055351
Expand Tier II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Human 95 Genes GS176616: HP:0000662 Night blindness
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Mouse 385 Genes GS135969: HDL QTL 6 (Hdlq6, Published QTL Chr 1)
Expand Tier I Mouse GO 4 Genes GS182620: GO:0002141 stereocilia ankle link
Expand Tier II Human 7486 Genes GS240624: [MeSH] Adaptor Proteins, Signal Transducing : D048868
Expand Tier II Human 7137 Genes GS234179: [MeSH] DNA, Intergenic : D021901
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 Mouse 467 Genes GS136771: SWR lupus locus 1 (Swrl1, Published QTL Chr 1)
Expand Tier I Mouse GO 1038 Genes GS180208: GO:0045595 regulation of cell differentiation
Expand Tier I Mouse 465 Genes GS135290: alcohol withdrawal 1 (Alcw1, Published QTL Chr 1)
Expand Tier II Human 686 Genes GS241459: [MeSH] Psychology, Social : D011593
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Mouse GO 980 Genes GS188826: GO:0022008 neurogenesis
Expand Tier II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 357 Genes GS237228: [MeSH] Eye Diseases, Hereditary : D015785
Expand Tier I Mouse 196 Genes GS230199: MSigDB Geneset - GSE13306_TREG_VS_TCONV_UP
Expand Tier I Mouse 460 Genes GS135578: cystic fibrosis modifier QTL 1 (Cfmq1, Published QTL Chr 1)
Expand Tier I Human GO 3116 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier II