Gene Details



Hs.75093 and homologs in 6 species are found in 941 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 II Human 2152 Genes GS234139: [MeSH] Biophysical Processes : D055597
Expand Tier I Mouse GO 335 Genes GS193273: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Mouse MP 157 Genes GS168313: MP:0000767 abnormal smooth muscle morphology
Expand Tier II Human 6358 Genes GS238474: [MeSH] Hormones : D006728
Expand Tier I Human GO 1682 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
Expand Tier I Mouse MP 18 Genes GS166687: MP:0009865 abnormal aorta smooth muscle morphology
Expand Tier II Human 6374 Genes GS243906: [MeSH] Metabolic Networks and Pathways : D053858
Expand Tier I Mouse 771 Genes GS135220: aromatase activity QTL 1 (Aaiq1, Published QTL Chr 4)
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 II Human 5416 Genes GS237717: [MeSH] Tissue Distribution : D014018
Expand Tier I Mouse GO 2260 Genes GS189855: GO:0043168 anion binding
Expand Tier II Human 8606 Genes GS243926: [MeSH] Exons : D005091
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier I Human 200 Genes GS230510: MSigDB Geneset - GSE3982_MAC_VS_BASOPHIL_UP
Expand Tier II Human 8563 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier I Human 60 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 267 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier II Human 11812 Genes GS236947: [MeSH] Brain : D001921
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier II Human 12069 Genes GS237417: [MeSH] Multigene Family : D005810
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse GO 919 Genes GS178388: GO:0055114 oxidation-reduction process
Expand Tier I Human CTD 2422 Genes GS123265: Estradiol interacting genes (MeSH:D004958) in CTD
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 52 Genes GS233389: KEGG Geneset - "Lysine degradation" pathway genes
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier II Human 10106 Genes GS234071: [MeSH] Protein Modification, Translational : D046188
Expand Tier II Human 15702 Genes GS245264: [MeSH] Nervous System : D009420
Expand Tier I Mouse 199 Genes GS227137: MSigDB Geneset - GSE27786_CD8_TCELL_VS_NKCELL_DN
Expand Tier II Human 3240 Genes GS236066: [MeSH] Musculoskeletal Physiological Phenomena : D009142
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 197 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 55 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier II Human 1685 Genes GS241253: [MeSH] Protein Folding : D017510
Expand Tier II Human 2639 Genes GS245025: [MeSH] Receptors, Cytokine : D018121
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier II Human 41 Genes GS236121: [MeSH] Glutarates : D005977
Expand Tier I Human 49 Genes GS231946: PC Geneset - "Lysine degradation" pathway genes
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier II Human 436 Genes GS240870: [MeSH] Bone Density : D015519
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 I Mouse 749 Genes GS136608: colon tumor susceptibility 11 (Scc11, Published QTL Chr 4)
Expand Tier I Human 323 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier II Human 1318 Genes GS245277: [MeSH] Catalysis : D002384
Expand Tier I Mouse 712 Genes GS136443: peak bone mineral density 3 (Pbmd3, Published QTL Chr 4)
Expand Tier I Mouse GO 4 Genes GS180175: GO:0070815 peptidyl-lysine 5-dioxygenase activity
Expand Tier II Human 1635 Genes GS237329: [MeSH] Acids, Acyclic : D000144
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier II Human 3419 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier II Human 7025 Genes GS239838: [MeSH] Luminescent Proteins : D008164
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 198 Genes GS227237: MSigDB Geneset - GSE22886_IGG_IGA_MEMORY_BCELL_VS_BLOOD_PLASMA_CELL_DN
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 339 Genes GS195494: GO:0006520 cellular amino acid metabolic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse 761 Genes GS136559: QTL for body weight independent of sex 1 (Qbis1, Published QTL Chr 4)
Expand Tier I Human GO 768 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Mouse GO 3597 Genes GS188142: GO:0048856 anatomical structure development
Expand Tier I Human 36 Genes GS228536: MSigDB Geneset - GNF2_PTX3
Expand Tier II Human 8197 Genes GS239290: [MeSH] Cell Line, Transformed : D002461
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
Expand Tier II Human 9719 Genes GS244871: [MeSH] Time Factors : D013997
Expand Tier I Mouse GO 82 Genes GS185827: GO:0051213 dioxygenase activity
Expand Tier II Human 1065 Genes GS237582: [MeSH] DEAD-box RNA Helicases : D053487
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 I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Mouse 712 Genes GS135460: bone mineral density 6 (Bomd6, Published QTL Chr 4)
Expand Tier I Mouse 766 Genes GS135509: body weight at 8 weeks QTL 2 (Bw8q2, Published QTL Chr 4)
Expand Tier II Human 4022 Genes GS234926: [MeSH] Epithelium : D004848
Expand Tier I Human GO 952 Genes GS202555: GO:0043436 oxoacid metabolic process
Expand Tier II Human 94 Genes GS242414: [MeSH] Collagen Diseases : D003095
Expand Tier II Human 12291 Genes GS238872: [MeSH] Central Nervous System : D002490
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier II Human 165 Genes GS238834: [MeSH] Triiodothyronine : D014284
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Human 86 Genes GS229599: MSigDB Geneset - GCTCTTG,MIR-335
Expand Tier I Human 41 Genes GS176789: HP:0100872 Abnormality of the plantar skin of foot
Expand Tier I Mouse 759 Genes GS135770: ear healing QTL 2 (Earheal2, Published QTL Chr 4)
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 260 Genes GS170933: HP:0001288 Gait disturbance
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier II Human 24839 Genes GS237194: [MeSH] Physiological Phenomena : D010829
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 I Human 28 Genes GS172164: HP:0001182 Tapered finger
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier II Human 908 Genes GS242101: [MeSH] Sexually Transmitted Diseases : D012749
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
Expand Tier I Human 198 Genes GS228197: MSigDB Geneset - GSE22886_IGA_VS_IGM_MEMORY_BCELL_DN
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Mouse MP 111 Genes GS170197: MP:0005592 abnormal vascular smooth muscle morphology
Expand Tier II Human 6955 Genes GS245398: [MeSH] Protein Isoforms : D020033
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human 155 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 47 Genes GS175737: HP:0001238 Slender finger
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 I Human GO 35 Genes GS204137: GO:0009066 aspartate family amino acid metabolic process
Expand Tier II Human 6568 Genes GS235980: [MeSH] Mechanical Phenomena : D055595
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 II Human 18300 Genes GS238771: [MeSH] Transferases : D014166
Expand Tier I Human 199 Genes GS227831: MSigDB Geneset - V$HSF_Q6
Expand Tier I Mouse GO 188 Genes GS184450: GO:0044420 extracellular matrix part
Expand Tier II Human 67130 Genes GS241889: [MeSH] Molecular Structure : D015394
Expand Tier I Human 169 Genes GS173988: HP:0000501 Glaucoma
Expand Tier III Mouse 7843 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier II Mouse 44 Genes GS35272: Hippocampus Gene expression correlates of Maximum startle response to 85 db in Females BXD
Expand Tier II Human 8187 Genes GS234648: [MeSH] Alleles : D000483
Expand Tier II Human 1779 Genes GS243727: [MeSH] SKP Cullin F-Box Protein Ligases : D044843
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 III Rat 497 Genes GS223177: Blood pressure QTL 210 (Bp210 Published QTL Chr 5)
Expand Tier I Mouse GO 152 Genes GS191271: GO:0018205 peptidyl-lysine modification
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier II Human 9312 Genes GS236231: [MeSH] Antigens : D000941
Expand Tier III Rat 804 Genes GS223676: Plasma insulin-like growth factor 1 level QTL 4 (Pigfal4 Published QTL Chr 5)
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier II Human 1261 Genes GS243450: [MeSH] Virus Physiological Phenomena : D018406
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 6357 Genes GS243210: [MeSH] Lysine : D008239
Expand Tier II Human 4947 Genes GS239154: [MeSH] Lymphocytes : D008214
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 10 Genes GS172435: HP:0002647 Aortic dissection
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 I Mouse 793 Genes GS136772: SGC/Knj cross B6 QTL 1 (Sxbq1, Published QTL Chr 4)
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier I Human GO 210 Genes GS208505: GO:0030198 extracellular matrix organization
Expand Tier I Human 188 Genes GS228055: MSigDB Geneset - CYCLIN_D1_KE_.V1_UP
Expand Tier I Mouse GO 154 Genes GS180298: GO:0005506 iron ion binding
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 I Human 4 Genes GS171676: HP:0003834 Shoulder dislocation
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier II Human 9078 Genes GS239596: [MeSH] Expressed Sequence Tags : D020224
Expand Tier II Human 5702 Genes GS236303: [MeSH] Ligases : D008025
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Mouse 771 Genes GS135350: Alzheimer's disease modifier 2 (Azdm2, Published QTL Chr 4)
Expand Tier II Human 1041 Genes GS239408: [MeSH] Pituitary Hormones : D010907
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 52 Genes GS174719: HP:0000774 Narrow chest
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 GO 84 Genes GS202664: GO:0051213 dioxygenase activity
Expand Tier I Human 263 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier II Human 13521 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Human 32 Genes GS229027: MSigDB Geneset - GNF2_MMP1
Expand Tier II Human 7632 Genes GS241002: [MeSH] Amino Acids, Essential : D000601
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Mouse MP 21 Genes GS164732: MP:0008438 abnormal cutaneous collagen fibril morphology
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
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 Mouse 712 Genes GS136191: light induced retinal degeneration 2 (Lrdg2, Published QTL Chr 4)
Expand Tier III Rat 637 Genes GS224594: Blood pressure QTL 103 (Bp103 Published QTL Chr 5)
Expand Tier I Mouse MP 1056 Genes GS169389: MP:0002060 abnormal skin morphology
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 14459 Genes GS239072: [MeSH] Recombinant Proteins : D011994
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 706 Genes GS198755: GO:0016491 oxidoreductase activity
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier I Human 73 Genes GS176571: HP:0008067 Abnormally lax or hyperextensible skin
Expand Tier II Human 2971 Genes GS237553: [MeSH] Sequence Tagged Sites : D016324
Expand Tier II Human 5 Genes GS235689: [MeSH] Hydroxylysine : D006901
Expand Tier I Mouse GO 122 Genes GS188395: GO:0019842 vitamin binding
Expand Tier II Human 14819 Genes GS244426: [MeSH] Tumor Cells, Cultured : D014407
Expand Tier II Human 8645 Genes GS234354: [MeSH] Cytoskeletal Proteins : D003598
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 200 Genes GS229330: MSigDB Geneset - HALLMARK_GLYCOLYSIS
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 1 Genes GS197083: GO:0046947 hydroxylysine biosynthetic process
Expand Tier II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier III Mouse 8331 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Human GO 2374 Genes GS206737: GO:0043168 anion binding
Expand Tier II Human 12343 Genes GS236576: [MeSH] Promoter Regions, Genetic : D011401
Expand Tier I Human 374 Genes GS229008: MSigDB Geneset - chr1p36
Expand Tier I Human 3 Genes GS173945: HP:0005952 Decreased pulmonary function
Expand Tier II Human 1426 Genes GS241252: [MeSH] Collagen : D003094
Expand Tier I Human 93 Genes GS170972: HP:0001933 Subcutaneous hemorrhage
Expand Tier I Human 100 Genes GS228108: MSigDB Geneset - CCCNNNNNNAAGWT_UNKNOWN
Expand Tier I Mouse MP 83 Genes GS169944: MP:0004142 abnormal muscle tone
Expand Tier I Human 382 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human CTD 307 Genes GS123854: Cyclophosphamide interacting genes (MeSH:D003520) in CTD
Expand Tier I Human GO 16 Genes GS198488: GO:0030867 rough endoplasmic reticulum membrane
Expand Tier I Human 13 Genes GS172297: HP:0001519 Disproportionate tall stature
Expand Tier I Mouse GO 2303 Genes GS177598: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
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 Human 219 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier III Rat 1467 Genes GS224712: Tongue tumor susceptibility QTL 11 (Tcas11 Published QTL Chr 5)
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 Mouse GO 2223 Genes GS182234: GO:0036211 protein modification process
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier II Human 9240 Genes GS237965: [MeSH] Peptide Hydrolases : D010447
Expand Tier II Human 2912 Genes GS243343: [MeSH] Amino Acids, Cyclic : D000598
Expand Tier I Human GO 267 Genes GS196679: GO:0030246 carbohydrate binding
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 Human 28 Genes GS173311: HP:0010651 Abnormality of the meninges
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 4977 Genes GS239472: [MeSH] Homeodomain Proteins : D018398
Expand Tier III Rat 1182 Genes GS224560: Serum cholesterol level QTL 20 (Scl20 Published QTL Chr 5)
Expand Tier I Mouse 758 Genes GS136148: lithogenic gene 8 (Lith8, Published QTL Chr 4)
Expand Tier I Mouse GO 1204 Genes GS188763: GO:0009888 tissue development
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier II Human 16 Genes GS245315: [MeSH] Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase : D008240
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Human 23 Genes GS231833: PC Geneset - "Other types of O-glycan biosynthesis" pathway genes
Expand Tier I Human 197 Genes GS227451: MSigDB Geneset - GSE3982_DC_VS_CENT_MEMORY_CD4_TCELL_UP
Expand Tier II Human 1210 Genes GS235850: [MeSH] Virus Physiological Processes : D055681
Expand Tier II Human 6617 Genes GS235747: [MeSH] Musculoskeletal and Neural Physiological Phenomena : D055687
Expand Tier II Human 10324 Genes GS234406: [MeSH] Multiprotein Complexes : D046912
Expand Tier II Human 2540 Genes GS235825: [MeSH] Oxygenases : D010105
Expand Tier II Human 5311 Genes GS237981: [MeSH] Leukocytes, Mononuclear : D007963
Expand Tier I Mouse 552 Genes GS135315: alcohol preference 3 QTL (Ap3q, Published QTL Chr 4)
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse 564 Genes GS135831: fluctuating asymmetry QTL 1 (Faq1, Published QTL Chr 4)
Expand Tier I Human GO 72 Genes GS198454: GO:0048029 monosaccharide binding
Expand Tier III Mouse 2256 Genes GS216489: Genes that are binding sites of CREB and zif268, transcription factors mediating neuronal activity and plasticity, in Mus musculus.
Expand Tier I Human GO 555 Genes GS195139: GO:0055114 oxidation-reduction process
Expand Tier I Mouse GO 2439 Genes GS179580: GO:0036094 small molecule binding
Expand Tier I Human GO 250 Genes GS201011: GO:0036293 response to decreased oxygen levels
Expand Tier I Human 187 Genes GS229202: MSigDB Geneset - CYCLIN_D1_UP.V1_UP
Expand Tier I Human 52 Genes GS233751: KEGG Geneset - "Lysine degradation" pathway genes
Expand Tier I Mouse 758 Genes GS135544: corpus callosum hemisphere surface size 2 (Ccrs2, Published QTL Chr 4)
Expand Tier I Mouse MP 722 Genes GS165612: MP:0002128 abnormal blood circulation
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Rat DRG 3886 Genes provisional GS86769: Table S2: HIPPOCAMPUS MGC MICROARRAY [DRG]
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 260 Genes GS172033: HP:0000369 Low-set ears
Expand Tier II Human 2308 Genes GS237932: [MeSH] Skin : D012867
Expand Tier I Mouse GO 2926 Genes GS183803: GO:0044267 cellular protein metabolic process
Expand Tier II Human 591 Genes GS239997: [MeSH] Hemorrhagic Disorders : D006474
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 II Human 2327 Genes GS241735: [MeSH] Molecular Weight : D008970
Expand Tier I Human 7 Genes GS175753: HP:0000015 Bladder diverticula
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier II Human 2696 Genes GS239584: [MeSH] Physicochemical Processes : D055606
Expand Tier I Human GO 247 Genes GS200142: GO:0001666 response to hypoxia
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 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 9 Genes GS175318: HP:0000563 Keratoconus
Expand Tier II Human 1785 Genes GS234677: [MeSH] Endonucleases : D004720
Expand Tier I Mouse MP 1743 Genes GS164263: MP:0002083 premature death
Expand Tier I Mouse MP 1967 Genes GS165616: MP:0002127 abnormal cardiovascular system morphology
Expand Tier I Human 37 Genes GS171851: HP:0000592 Blue sclerae
Expand Tier II Human 11221 Genes GS237257: [MeSH] Pathologic Processes : D010335
Expand Tier I Mouse MP 1548 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier II Mouse 594 Genes GS84321: pentobarbital withdrawal Chr4 (Published QTL)
Expand Tier I Human GO 82 Genes GS209317: GO:0016702 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen
Expand Tier II Human 1896 Genes GS237199: [MeSH] Chromosomes, Human, 1-3 : D002900
Expand Tier I Human GO 18 Genes GS204136: GO:0009067 aspartate family amino acid biosynthetic process
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
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 440 Genes GS231777: PC Geneset - "RGAANNTTC_V$HSF1_01" pathway genes
Expand Tier I Human 257 Genes GS232404: PC Geneset - "Extracellular matrix organization" pathway genes
Expand Tier I Human CTD 212 Genes GS124295: Polychlorinated Biphenyls interacting genes (MeSH:D011078) in CTD
Expand Tier I Human 33 Genes GS174067: HP:0002904 Hyperbilirubinemia
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier II Human 2398 Genes GS235868: [MeSH] Carboxylic Acids : D002264
Expand Tier II Human 7014 Genes GS240404: [MeSH] Immune System : D007107
Expand Tier II Human 20775 Genes GS245804: [MeSH] Transcription Factors : D014157
Expand Tier II Human 23211 Genes GS235538: [MeSH] Protein Binding : D011485
Expand Tier II Human 8081 Genes GS245560: [MeSH] Ubiquitin : D025801
Expand Tier II Mouse 513 Genes GS84165: ethanol conditioned taste aversion (Published QTL, Chr 4)
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
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 II Human 10133 Genes GS235960: [MeSH] Connective Tissue Cells : D003239
Expand Tier II Human 5399 Genes GS243780: [MeSH] COS Cells : D019556
Expand Tier I Human GO 61 Genes GS208235: GO:0008652 cellular amino acid biosynthetic process
Expand Tier II Human 6306 Genes GS235691: [MeSH] Multienzyme Complexes : D009097
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 56 Genes GS175070: HP:0000973 Cutis laxa
Expand Tier II Mouse 731 Genes GS83998: cocaine and amphetamine-regulated transcript QTL 2 (Crq2, Published QTL, Chr 4)
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 38 Genes GS171381: HP:0001558 Decreased fetal movement
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier I Human GO 211 Genes GS195507: GO:0043062 extracellular structure organization
Expand Tier II Human 3577 Genes GS234895: [MeSH] Zebrafish Proteins : D029961
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier II Human 1649 Genes GS242013: [MeSH] Gene Duplication : D020440
Expand Tier I Mouse 758 Genes GS136150: "lupus in MRL and B6 F2 cross, QTL 1" (Lmb1, Published QTL Chr 4)
Expand Tier I Human 199 Genes GS229046: MSigDB Geneset - GSE22886_NAIVE_CD8_TCELL_VS_DC_DN
Expand Tier I Human 86 Genes GS174810: HP:0001635 Congestive heart failure
Expand Tier II Human 4900 Genes GS245843: [MeSH] Proteasome Endopeptidase Complex : D046988
Expand Tier I Human GO 3 Genes GS197428: GO:0008475 procollagen-lysine 5-dioxygenase activity
Expand Tier II Human 58766 Genes GS243866: [MeSH] Laboratory Chemicals : D019995
Expand Tier II Human 1210 Genes GS245013: [MeSH] Connective Tissue Diseases : D003240
Expand Tier I Human 129 Genes GS173792: HP:0002815 Abnormality of the knees
Expand Tier I Mouse MP 2112 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human 52 Genes GS174808: HP:0001633 Abnormality of the mitral valve
Expand Tier I Human 12202 Genes GS232685: PC Geneset - "Homo sapiens" pathway genes
Expand Tier II Human 2194 Genes GS235041: [MeSH] Glycosyltransferases : D016695
Expand Tier III Rat 804 Genes GS223922: Body weight QTL 148 (Bw148 Published QTL Chr 5)
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 II Human 15342 Genes GS242876: [MeSH] Proteome : D020543
Expand Tier I Human 193 Genes GS230001: MSigDB Geneset - GSE37416_0H_VS_24H_F_TULARENSIS_LVS_NEUTROPHIL_UP
Expand Tier I Human 58 Genes GS171388: HP:0001557 Prenatal movement abnormality
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier III Rat 1295 Genes GS224319: Blood pressure QTL 7 (Bp7 Published QTL Chr 5)
Expand Tier II Human 425 Genes GS237688: [MeSH] Cathepsins : D002403
Expand Tier I Mouse 758 Genes GS136705: systemic lupus erythmatosus suppressor 2 (Sles2, Published QTL Chr 4)
Expand Tier I Mouse MP 11449 Genes GS164136: MP:0000001 mammalian phenotype
Expand Tier II Human 867 Genes GS245305: [MeSH] Sexually Transmitted Diseases, Viral : D015229
Expand Tier III Rat 201 Genes GS224983: Blood pressure QTL 155 (Bp155 Published QTL Chr 5)
Expand Tier I Mouse MP 1057 Genes GS166117: MP:0002108 abnormal muscle morphology
Expand Tier I Mouse MP 11 Genes GS166730: MP:0004044 aortic dissection
Expand Tier I Human GO 259 Genes GS195145: GO:0016053 organic acid biosynthetic process
Expand Tier I Human 199 Genes GS230003: MSigDB Geneset - GSE29618_PRE_VS_DAY7_POST_TIV_FLU_VACCINE_PDC_UP
Expand Tier I Mouse 694 Genes GS135567: cytokine deficiency colitis susceptibility 9 (Cdcs9, Published QTL Chr 4)
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 Mouse 552 Genes GS136621: sucrose consumption 2 (Scon2, Published QTL Chr 4)
Expand Tier II Human 2219 Genes GS238955: [MeSH] Protein Interaction Domains and Motifs : D054730
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse MP 578 Genes GS168151: MP:0001914 hemorrhage
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier II Human 3712 Genes GS235130: [MeSH] Gene Expression Regulation, Enzymologic : D015971
Expand Tier II Human 2584 Genes GS235299: [MeSH] Physical Processes : D055586
Expand Tier I Human 2 Genes GS176961: HP:0001020 Soft, thin skin
Expand Tier II Human 6347 Genes GS238775: [MeSH] Animal Structures : D000825
Expand Tier I Human 122 Genes GS173563: HP:0000692 Misalignment of teeth
Expand Tier I Mouse GO 13 Genes GS191852: GO:0008198 ferrous iron binding
Expand Tier II Human 3803 Genes GS243242: [MeSH] Skin Diseases : D012871
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier II Human 11797 Genes GS236666: [MeSH] Gene Silencing : D020868
Expand Tier II Human 8246 Genes GS234669: [MeSH] Cell Cycle Proteins : D018797
Expand Tier I Mouse 766 Genes GS135893: gastritis type A susceptibility locus 1 (Gasa1, Published QTL Chr 4)
Expand Tier II Human 1561 Genes GS239336: [MeSH] Golgi Apparatus : D006056
Expand Tier I Mouse 534 Genes GS128576: Ethanol induced LORR Chr# 4
Expand Tier II Mouse 45 Genes GS35262: Hippocampus Gene expression correlates of Maximum startle response to 80 db in Females BXD
Expand Tier I Mouse GO 219 Genes GS179910: GO:0030246 carbohydrate binding
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human 44 Genes GS172038: HP:0000963 Thin skin
Expand Tier II Human 2939 Genes GS235971: [MeSH] Vascular Diseases : D014652
Expand Tier I Human CTD 5081 Genes GS126276: pirinixic acid interacting genes (MeSH:C006253) in CTD
Expand Tier I Mouse MP 51 Genes GS166790: MP:0009873 abnormal aorta tunica media morphology
Expand Tier I Human 60 Genes GS171207: HP:0000098 Tall stature
Expand Tier II Human 1538 Genes GS243791: [MeSH] Intracellular Membranes : D007425
Expand Tier I Mouse 780 Genes GS136719: susceptibility to lung cancer 21 (Sluc21, Published QTL Chr 4)
Expand Tier I Mouse GO 87 Genes GS181440: GO:0005581 collagen
Expand Tier I Human 9 Genes GS172309: HP:0100692 Increased corneal curvature
Expand Tier II Human 268 Genes GS239368: [MeSH] Thyroid Hormones : D013963
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human 88 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier II Human 2400 Genes GS245620: [MeSH] Amino Acids, Aromatic : D024322
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 Mouse 636 Genes GS135899: granulosa cell tumorigenesis 1 (Gct1, Published QTL Chr 4)
Expand Tier I Human 199 Genes GS227634: MSigDB Geneset - GSE10325_LUPUS_BCELL_VS_LUPUS_MYELOID_DN
Expand Tier I Mouse GO 19 Genes GS188459: GO:0031418 L-ascorbic acid binding
Expand Tier III Rat 627 Genes GS224377: Sensitivity to stroke QTL 2 (Strs2 Published QTL Chr 5)
Expand Tier I Human 173 Genes GS175117: HP:0001883 Talipes
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier II Human 4197 Genes GS239331: [MeSH] Histones : D006657
Expand Tier II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Mouse 771 Genes GS135775: epistatic circling B C57L/J (Eclb, Published QTL Chr 4)
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier II Human 73 Genes GS235131: [MeSH] Galactosyltransferases : D005700
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 50 Genes GS175148: HP:0010511 Long toe
Expand Tier II Human 7137 Genes GS234179: [MeSH] DNA, Intergenic : D021901
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 161 Genes GS202464: GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
Expand Tier II Mouse 513 Genes GS84166: METH responses for climbing (Published QTL, Chr 4)
Expand Tier III Rat 823 Genes GS223957: Cardiac mass QTL 64 (Cm64 Published QTL Chr 5)
Expand Tier II Human 3642 Genes GS239875: [MeSH] Immune System Diseases : D007154
Expand Tier II Human 8998 Genes GS240602: [MeSH] Biological Markers : D015415
Expand Tier I Mouse MP 1235 Genes GS170198: MP:0001614 abnormal blood vessel morphology
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 2342 Genes GS241507: [MeSH] Mixed Function Oxygenases : D006899
Expand Tier II Human 10952 Genes GS241962: [MeSH] RNA Interference : D034622
Expand Tier II Human 9229 Genes GS243125: [MeSH] Organic Chemicals : D009930
Expand Tier II Human 2643 Genes GS238924: [MeSH] Membranes : D008566
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier I Mouse GO 45 Genes GS190971: GO:0016706 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, 2-oxoglutarate as one donor, and incorporation of one atom each of oxygen into both donors
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Human 2176 Genes GS235901: [MeSH] Mesoderm : D008648
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 Human GO 259 Genes GS200383: GO:0046394 carboxylic acid biosynthetic process
Expand Tier I Human GO 845 Genes GS204326: GO:0019752 carboxylic acid metabolic process
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier II Human 7027 Genes GS238294: [MeSH] Amino Acids, Basic : D024361
Expand Tier II Human 3071 Genes GS237070: [MeSH] Biophysical Phenomena : D055592
Expand Tier I Human 159 Genes GS175096: HP:0000286 Epicanthus
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
Expand Tier II Human 9232 Genes GS245445: [MeSH] Stem Cells : D013234
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier I Human 86 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier II Human 58262 Genes GS240750: [MeSH] Molecular Probes : D015335
Expand Tier I Human 199 Genes GS227358: MSigDB Geneset - HALLMARK_EPITHELIAL_MESENCHYMAL_TRANSITION
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier II Human 140 Genes GS239671: [MeSH] Thyrotropin : D013972
Expand Tier I Human CTD 48 Genes GS123568: 4-hydroxy-equilenin interacting genes (MeSH:C065250) in CTD
Expand Tier II Human 607 Genes GS235262: [MeSH] Anaphase-Promoting Complex-Cyclosome : D064173
Expand Tier I Mouse GO 2 Genes GS184443: GO:0017185 peptidyl-lysine hydroxylation
Expand Tier I Human CTD 5732 Genes GS127240: Acetaminophen interacting genes (MeSH:D000082) in CTD
Expand Tier I Mouse 694 Genes GS136860: thermal pain response 1 (Tpnr1, Published QTL Chr 4)
Expand Tier II Human 4244 Genes GS234130: [MeSH] Genetic Diseases, Inborn : D030342
Expand Tier I Human GO 856 Genes GS194645: GO:0042802 identical protein binding
Expand Tier I Human 200 Genes GS227969: MSigDB Geneset - GSE24634_IL4_VS_CTRL_TREATED_NAIVE_CD4_TCELL_DAY5_UP
Expand Tier II Human 3013 Genes GS240174: [MeSH] Isoenzymes : D007527
Expand Tier I Rat 51 Genes GS233254: KEGG Geneset - "Lysine degradation" pathway genes
Expand Tier II Human 4107 Genes GS234842: [MeSH] Peptide Fragments : D010446
Expand Tier II Human 917 Genes GS243243: [MeSH] Pituitary Hormones, Anterior : D010908
Expand Tier I Mouse 760 Genes GS136730: susceptibility to lung cancer 6 (Sluc6, Published QTL Chr 4)
Expand Tier I Human 147 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier II Human 55514 Genes GS238409: [MeSH] Gene Components : D040461
Expand Tier I Mouse 552 Genes GS135480: bone response to mechanical loading 13 (Brml13, Published QTL Chr 4)
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Human 80 Genes GS172248: HP:0001373 Joint dislocation
Expand Tier II Human 87 Genes GS237441: [MeSH] Procollagen-Proline Dioxygenase : D011393
Expand Tier II Human 5263 Genes GS236400: [MeSH] Receptors, Immunologic : D011971
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier II Human 13620 Genes GS234949: [MeSH] Genetic Vectors : D005822
Expand Tier I Human GO 453 Genes GS194627: GO:0008544 epidermis development
Expand Tier I Mouse GO 1572 Genes GS192354: GO:0046914 transition metal ion binding
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier II Human 5213 Genes GS244078: [MeSH] Ubiquitin-Protein Ligase Complexes : D043743
Expand Tier I Mouse 757 Genes GS135477: bone response to mechanical loading 10 (Brml10, Published QTL Chr 4)
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier II Human 1235 Genes GS241194: [MeSH] RNA Helicases : D020365
Expand Tier I Mouse 199 Genes GS228004: MSigDB Geneset - GSE20715_WT_VS_TLR4_KO_48H_OZONE_LUNG_UP
Expand Tier II Human 1432 Genes GS235231: [MeSH] Bone and Bones : D001842
Expand Tier II Human 15426 Genes GS239526: [MeSH] Phosphotransferases : D010770
Expand Tier I Mouse 564 Genes GS135920: graft-versus host disease 5 (Gvhd5, Published QTL Chr 4)
Expand Tier II Human 36 Genes GS237924: [MeSH] Ehlers-Danlos Syndrome : D004535
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 173 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier II Human 8519 Genes GS243346: [MeSH] Chromosomes, Human : D002877
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier II Human 13250 Genes GS238537: [MeSH] Pharmacological Phenomena : D002620
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 7799 Genes GS238638: [MeSH] Esterases : D004950
Expand Tier I Human 14 Genes GS175066: HP:0000977 Soft skin
Expand Tier II Human 32928 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier I Human GO 6743 Genes