Gene Details



Hs.408702 and homologs in 7 species are found in 494 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 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 130 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier II Human 19667 Genes GS245646: [MeSH] Hydrolases : D006867
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier II Human 83 Genes GS245459: [MeSH] Neutropenia : D009503
Expand Tier I Mouse GO 244 Genes GS185386: GO:0008380 RNA splicing
Expand Tier II Human 22403 Genes GS244084: [MeSH] Phenotype : D010641
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier III Rat 275 Genes GS224402: Food consumption QTL 7 (Foco7 Published QTL Chr 19)
Expand Tier III Rat 588 Genes GS224085: Body weight QTL 152 (Bw152 Published QTL Chr 19)
Expand Tier I Mouse 574 Genes GS136137: lithogenic gene 18 (Lith18, Published QTL Chr 8)
Expand Tier I Mouse 200 Genes GS227253: MSigDB Geneset - GSE17721_12H_VS_24H_LPS_BMDM_UP
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier II Human 12421 Genes GS239540: [MeSH] Heterochromatin : D006570
Expand Tier I Mouse 198 Genes GS229590: MSigDB Geneset - GSE17721_POLYIC_VS_GARDIQUIMOD_24H_BMDM_UP
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse 573 Genes GS136045: insulin dependent diabetes susceptibility 22 (Idd22, Published QTL Chr 8)
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier II Human 14353 Genes GS244882: [MeSH] Epithelial Cells : D004847
Expand Tier II Human 8563 Genes GS234210: [MeSH] HeLa Cells : D006367
Expand Tier III Rat 404 Genes GS224167: Cardiac mass QTL 9 (Cm9 Published QTL Chr 19)
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier II Human 8182 Genes GS240575: [MeSH] RNA, Small Untranslated : D058727
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 100 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Mouse 200 Genes GS227478: MSigDB Geneset - GSE17721_PAM3CSK4_VS_GADIQUIMOD_8H_BMDM_DN
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse 573 Genes GS135547: CD4 T cell subset 3 (Cd4ts3, Published QTL Chr 8)
Expand Tier I Human 110 Genes GS171784: HP:0001399 Hepatic failure
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 GO 23778 Genes GS193268: GO:0005575 cellular_component
Expand Tier II Human 4661 Genes GS238716: [MeSH] Genetic Linkage : D008040
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 137 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier II Human 12580 Genes GS238462: [MeSH] Interspersed Repetitive Sequences : D020071
Expand Tier II Human 15224 Genes GS234359: [MeSH] Reproduction : D012098
Expand Tier III Mouse 542 Genes GS216887: Co-expression cluster of haloperidol-induced catalepsy genes in striatum of HS mice short term selected lines. Grey Cluster
Expand Tier I Human 249 Genes GS232165: PC Geneset - "V$GABP_B" pathway genes
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier II Human 70252 Genes GS238030: [MeSH] Chemical Phenomena : D055598
Expand Tier I Human 32 Genes GS174840: HP:0011358 Generalized hypopigmentation of hair
Expand Tier I Human 197 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Mouse 451 Genes GS135840: femoral bone trait QTL 3 (Fbtq3, Published QTL Chr 8)
Expand Tier I Human 282 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 55 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse 574 Genes GS135948: HDL QTL 16 (Hdlq16, Published QTL Chr 8)
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier III Rat 592 Genes GS223838: Urinary albumin excretion QTL 39 (Uae39 Published QTL Chr 19)
Expand Tier I Mouse 198 Genes GS227766: MSigDB Geneset - GSE17721_PAM3CSK4_VS_CPG_6H_BMDM_DN
Expand Tier II Human 446 Genes GS245783: [MeSH] Genetic Diseases, X-Linked : D040181
Expand Tier I Human 11 Genes GS176359: HP:0001029 Poikiloderma
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 263 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier II Human 30225 Genes GS236481: [MeSH] Enzymes : D004798
Expand Tier I Human 87 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Mouse 501 Genes GS136657: skeletal muscle weight 16 (Skmw16, Published QTL Chr 8)
Expand Tier I Human 118 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 195 Genes GS230414: MSigDB Geneset - GSE9988_ANTI_TREM1_VS_VEHICLE_TREATED_MONOCYTES_DN
Expand Tier I Human 2430 Genes GS231626: PC Geneset - "CAGGTG_V$E12_Q6" pathway genes
Expand Tier I Mouse 200 Genes GS228871: MSigDB Geneset - GSE17721_0.5H_VS_12H_PAM3CSK4_BMDM_DN
Expand Tier I Human 187 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human 124 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier II Human 3419 Genes GS234275: [MeSH] Heterozygote : D006579
Expand Tier I Mouse 445 Genes GS136061: immunoregulatory 3 (Im3, Published QTL Chr 8)
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
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 II Human 2660 Genes GS244236: [MeSH] Homozygote : D006720
Expand Tier I Human 37 Genes GS176711: HP:0100585 Teleangiectasia of the skin
Expand Tier I Mouse GO 3599 Genes GS186227: GO:0090304 nucleic acid metabolic process
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 Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human 300 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Mouse 200 Genes GS227930: MSigDB Geneset - GSE17721_0.5H_VS_4H_PAM3CSK4_BMDM_DN
Expand Tier I Human 192 Genes GS229305: MSigDB Geneset - GSE2706_UNSTIM_VS_8H_LPS_AND_R848_DC_UP
Expand Tier I Mouse GO 524 Genes GS180942: GO:0006396 RNA processing
Expand Tier I Human 112 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier II Human 9980 Genes GS243345: [MeSH] Alternative Splicing : D017398
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 II Human 37746 Genes GS240208: [MeSH] Amino Acid Sequence : D000595
Expand Tier I Mouse 199 Genes GS228655: MSigDB Geneset - GSE17721_LPS_VS_GARDIQUIMOD_1H_BMDM_DN
Expand Tier I Human 2460 Genes GS229573: MSigDB Geneset - CAGGTG_V$E12_Q6
Expand Tier II Human 30100 Genes GS238002: [MeSH] Antisense Elements (Genetics) : D016375
Expand Tier I Human 342 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier II Human 35836 Genes GS242639: [MeSH] Metabolic Phenomena : D055754
Expand Tier II Human 429 Genes GS235357: [MeSH] RNA, Small Nuclear : D012342
Expand Tier I Mouse 2 Genes GS231200: OMIM Geneset - Genes with known associations to "Poikiloderma with neutropenia"
Expand Tier III Rat 526 Genes GS223124: Insulin/glucose ratio QTL 8 (Insglur8 Published QTL Chr 19)
Expand Tier II Human 18727 Genes GS236759: [MeSH] Intranuclear Space : D042581
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Mouse 460 Genes GS135482: bone response to mechanical loading 2 (Brml2, Published QTL Chr 8)
Expand Tier I Human 2892 Genes GS232583: PC Geneset - "GGGCGGR_V$SP1_Q6" pathway genes
Expand Tier I Human 19 Genes GS176420: HP:0100671 Abnormal trabecular bone morphology
Expand Tier I Human 194 Genes GS230194: MSigDB Geneset - GSE22886_IGM_MEMORY_BCELL_VS_BLOOD_PLASMA_CELL_UP
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 136 Genes GS227640: MSigDB Geneset - AGGGCAG,MIR-18A
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Human 75 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier I Mouse 573 Genes GS135883: femur geometry 7 (Fmgty7, Published QTL Chr 8)
Expand Tier II Human 14860 Genes GS240463: [MeSH] Chromatin : D002843
Expand Tier II Human 61866 Genes GS235287: [MeSH] Proteins : D011506
Expand Tier I Human 1196 Genes GS230355: MSigDB Geneset - SCGGAAGY_V$ELK1_02
Expand Tier II Human 46864 Genes GS243659: [MeSH] RNA, Messenger : D012333
Expand Tier I Mouse 199 Genes GS230802: MSigDB Geneset - GSE9037_CTRL_VS_LPS_4H_STIM_BMDM_DN
Expand Tier II Human 13620 Genes GS234949: [MeSH] Genetic Vectors : D005822
Expand Tier III Rat 588 Genes GS223913: Serum leptin concentration QTL 13 (Slep13 Published QTL Chr 19)
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier II Human 12282 Genes GS234930: [MeSH] Genes, Insect : D017344
Expand Tier I Human 220 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human 56 Genes GS176765: HP:0001009 Telangiectasia
Expand Tier I Human 54 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier II Human 56846 Genes GS235305: [MeSH] DNA, Complementary : D018076
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier II Human 361 Genes GS237540: [MeSH] Infant, Newborn, Diseases : D007232
Expand Tier I Human 116 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 113 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier II Human 4450 Genes GS236040: [MeSH] Nutritional and Metabolic Diseases : D009750
Expand Tier I Human 25 Genes GS175546: HP:0010885 Aseptic necrosis
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier II Human 39830 Genes GS245976: [MeSH] Cellular Structures : D022082
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier II Human 67553 Genes GS240572: [MeSH] DNA : D004247
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 31495 Genes GS241930: [MeSH] Mutation : D009154
Expand Tier I Human 42 Genes GS173130: HP:0001875 Neutropenia
Expand Tier II Human 73890 Genes GS239190: [MeSH] Genome : D016678
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 13 Genes GS206565: GO:0016180 snRNA processing
Expand Tier I Mouse GO 13 Genes GS189688: GO:0016180 snRNA processing
Expand Tier II Human 7799 Genes GS238638: [MeSH] Esterases : D004950
Expand Tier II Human 32928 Genes GS234668: [MeSH] Open Reading Frames : D016366
Expand Tier I Mouse 501 Genes GS136755: susceptibility to Salmonella typhimurium antigens 6 (Ssta6, Published QTL Chr 8)
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier II Human 20510 Genes GS237794: [MeSH] Oligodeoxyribonucleotides : D009838
Expand Tier I Mouse 455 Genes GS136572: radiation induced acute myeloid leukemia 4 (Raml4, Published QTL Chr 8)
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Mouse GO 1 Genes GS193359: GO:0034477 U6 snRNA 3'-end processing
Expand Tier II Human 43280 Genes GS236911: [MeSH] Transcription, Genetic : D014158
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier II Human 65203 Genes GS235942: [MeSH] Genetic Processes : D039361
Expand Tier II Human 13292 Genes GS238111: [MeSH] Genotype : D005838
Expand Tier I Mouse GO 192 Genes GS193365: GO:0034470 ncRNA processing
Expand Tier I Human GO 607 Genes GS203909: GO:0016071 mRNA metabolic process
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier II Human 365 Genes GS237474: [MeSH] Leukocyte Disorders : D007960
Expand Tier I Mouse GO 247 Genes GS182492: GO:0034660 ncRNA metabolic process
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse 718 Genes GS128597: Ethanol Induced Ataxia Chr#8
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier II Human 16267 Genes GS243838: [MeSH] Nuclear Proteins : D009687
Expand Tier I Human 1875 Genes GS227234: MSigDB Geneset - AACTTT_UNKNOWN
Expand Tier I Human 211 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier II Human 30317 Genes GS239295: [MeSH] Enzymes and Coenzymes : D045762
Expand Tier I Human 1211 Genes GS232118: PC Geneset - "SCGGAAGY_V$ELK1_02" pathway genes
Expand Tier I Human 66 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier II Human 79329 Genes GS243722: [MeSH] Genetic Structures : D040342
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier II Human 56931 Genes GS241744: [MeSH] DNA, Single-Stranded : D004277
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 56 Genes GS174179: HP:0002514 Cerebral calcification
Expand Tier II Human 20981 Genes GS241565: [MeSH] Polynucleotides : D011119
Expand Tier II Human 30254 Genes GS243763: [MeSH] Intracellular Space : D042541
Expand Tier I Mouse 460 Genes GS135513: "body weight, QTL 3" (Bwq3, Published QTL Chr 8)
Expand Tier I Human 121 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 78 Genes GS173387: HP:0002757 Recurrent fractures
Expand Tier I Mouse 542 Genes GS135540: cerebellum weight 2 (Cbm2, Published QTL Chr 8)
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 197 Genes GS229527: MSigDB Geneset - GSE37416_12H_VS_24H_F_TULARENSIS_LVS_NEUTROPHIL_UP
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 23 Genes GS173554: HP:0005374 Cellular immunodeficiency
Expand Tier II Human 13600 Genes GS235415: [MeSH] Embryo, Mammalian : D004622
Expand Tier II Human 13895 Genes GS244414: [MeSH] Arthropod Proteins : D060829
Expand Tier I Human 75 Genes GS175692: HP:0200042 Skin ulcer
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 126 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier II Human 315 Genes GS235764: [MeSH] Chromosomes, Human, Pair 16 : D002885
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 Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 289 Genes GS199289: GO:0034660 ncRNA metabolic process
Expand Tier II Human 73218 Genes GS245795: [MeSH] Genes : D005796
Expand Tier I Mouse 453 Genes GS136356: novelty/stress induced locomotor activation 7 (Nsila7, Published QTL Chr 8)
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 310 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 44 Genes GS229430: MSigDB Geneset - chr16q13
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Mouse 519 Genes GS136533: preaxial shift (Prxsh, Published QTL Chr 8)
Expand Tier III Rat 526 Genes GS224976: Serum corticosterone level QTL 11 (Scort11 Published QTL Chr 19)
Expand Tier II Human 8099 Genes GS236751: [MeSH] Polymorphism, Single Nucleotide : D020641
Expand Tier I Human 110 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human 282 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 174 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier II Human 47536 Genes GS236298: [MeSH] Gene Expression : D015870
Expand Tier III Rat 429 Genes GS224573: Bone structure and strength QTL 8 (Bss8 Published QTL Chr 19)
Expand Tier I Human GO 8 Genes GS208848: GO:0043628 ncRNA 3'-end processing
Expand Tier II Human 18907 Genes GS242148: [MeSH] Cell Nucleus Structures : D022003
Expand Tier I Human 45 Genes GS175084: HP:0008384 Aplastic/hypoplastic fingernail
Expand Tier I Mouse GO 15 Genes GS187048: GO:0016073 snRNA metabolic process
Expand Tier II Human 1627 Genes GS237683: [MeSH] Hematologic Diseases : D006402
Expand Tier II Human 13815 Genes GS240409: [MeSH] Drosophila Proteins : D029721
Expand Tier II Human 33265 Genes GS237679: [MeSH] Genetic Code : D005815
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier II Human 2405 Genes GS238714: [MeSH] Hemic and Lymphatic Diseases : D006425
Expand Tier I Mouse 200 Genes GS228973: MSigDB Geneset - GSE17721_PAM3CSK4_VS_GADIQUIMOD_1H_BMDM_DN
Expand Tier II Human 13886 Genes GS245484: [MeSH] Insect Proteins : D019476
Expand Tier I Human 196 Genes GS229269: MSigDB Geneset - GSE3982_EFF_MEMORY_CD4_TCELL_VS_NKCELL_DN
Expand Tier I Mouse 574 Genes GS136313: non-HDL QTL 1 (Nhdlq1, Published QTL Chr 8)
Expand Tier I Mouse 199 Genes GS228611: MSigDB Geneset - GSE17721_POLYIC_VS_GARDIQUIMOD_1H_BMDM_DN
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier II Human 35136 Genes GS240987: [MeSH] Metabolism : D008660
Expand Tier I Human 356 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier II Human 5 Genes GS244755: [MeSH] Rothmund-Thomson Syndrome : D011038
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Mouse 586 Genes GS135989: Hfe modifier 2 (Hfem2, Published QTL Chr 8)
Expand Tier II Human 36279 Genes GS241850: [MeSH] Genetic Variation : D014644
Expand Tier III Rat 576 Genes GS223504: Urinary albumin excretion QTL 19 (Uae19 Published QTL Chr 19)
Expand Tier I Human 79 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier III Rat 788 Genes GS223499: Urinary albumin excretion QTL 12 (Uae12 Published QTL Chr 19)
Expand Tier I Human 104 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier II Human 12246 Genes GS243456: [MeSH] Euchromatin : D022041
Expand Tier I Human 243 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier II Human 38809 Genes GS236076: [MeSH] Protein Conformation : D011487
Expand Tier II Human 11662 Genes GS239443: [MeSH] RNA Splicing : D012326
Expand Tier II Human 21260 Genes GS238232: [MeSH] Nucleoproteins : D009698
Expand Tier I Mouse GO 45 Genes GS193504: GO:0031123 RNA 3'-end processing
Expand Tier II Human 523 Genes GS234070: [MeSH] Skin Diseases, Genetic : D012873
Expand Tier II Human 15356 Genes GS234761: [MeSH] Reproductive Physiological Processes : D055704
Expand Tier I Human 258 Genes GS227160: MSigDB Geneset - V$GABP_B
Expand Tier II Human 15662 Genes GS235446: [MeSH] Reproductive and Urinary Physiological Phenomena : D012101
Expand Tier II Human 15 Genes GS240791: [MeSH] Dyskeratosis Congenita : D019871
Expand Tier II Human 22746 Genes GS237337: [MeSH] Nucleotides : D009711
Expand Tier I Mouse 449 Genes GS135259: autoimmune extremity vasculitis in MRL mice 1 (Aevm1, Published QTL Chr 8)
Expand Tier I Mouse 456 Genes GS136059: Immunoregulatory 1 (Im1, Published QTL Chr 8)
Expand Tier I Human 65 Genes GS171788: HP:0001394 Cirrhosis
Expand Tier II Mouse 558 Genes GS84206: METH responses for body temperature (Published QTL, Chr 8)
Expand Tier I Human 42 Genes GS173577: HP:0011991 Abnormal neutrophil cell number
Expand Tier I Mouse 573 Genes GS136068: immune response to AAV2 QTL 2 (Imraq2, Published QTL Chr 8)
Expand Tier I Mouse 200 Genes GS228170: MSigDB Geneset - GSE17721_LPS_VS_GARDIQUIMOD_24H_BMDM_UP
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Mouse 586 Genes GS135972: wound healing/regeneration 1 (Heal1, Published QTL Chr 8)
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 153 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier II Human 3936 Genes GS245455: [MeSH] Metabolic Diseases : D008659
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human GO 93 Genes GS210451: GO:0031123 RNA 3'-end processing
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse 573 Genes GS135613: circulating hormone level QTL 5 (Chlq5, Published QTL Chr 8)
Expand Tier I Human 94 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier II Human 13521 Genes GS245544: [MeSH] Conserved Sequence : D017124
Expand Tier I Human 226 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Mouse 199 Genes GS227747: MSigDB Geneset - GSE17721_PAM3CSK4_VS_GADIQUIMOD_24H_BMDM_DN
Expand Tier I Mouse 200 Genes GS229931: MSigDB Geneset - GSE17721_PAM3CSK4_VS_GADIQUIMOD_16H_BMDM_DN
Expand Tier I Human 161 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier II Human 9287 Genes GS243335: [MeSH] Chromosomes, Mammalian : D033481
Expand Tier I Human 38 Genes GS171916: HP:0002665 Lymphoma
Expand Tier II Human 30749 Genes GS236775: [MeSH] RNA, Untranslated : D022661
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier III Mouse 5790 Genes GS213077: Genes with suggestive difference in (PWD) vs (PB6F1 + B6PF1 + B6) comparison
Expand Tier I Human GO 652 Genes GS197734: GO:0006396 RNA processing
Expand Tier I Human 78 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 101 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Mouse 200 Genes GS227598: MSigDB Geneset - GSE17721_0.5H_VS_8H_PAM3CSK4_BMDM_DN
Expand Tier II Human 299 Genes GS236230: [MeSH] Skin Abnormalities : D012868
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier II Human 28680 Genes GS238990: [MeSH] Mathematical Concepts : D055641
Expand Tier II Human 50108 Genes GS239769: [MeSH] Gene Library : D015723
Expand Tier II Human 26319 Genes GS238348: [MeSH] Cell Line : D002460
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 326 Genes GS202209: GO:0008380 RNA splicing
Expand Tier I Human 263 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier II Human 84 Genes GS234756: [MeSH] Agranulocytosis : D000380
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 2 Genes GS199382: GO:0034472 snRNA 3'-end processing
Expand Tier II Human 29996 Genes GS237597: [MeSH] Cell Physiological Processes : D055648
Expand Tier III Rat 591 Genes GS223227: Alcohol response QTL 21 (Alcrsp21 Published QTL Chr 19)
Expand Tier I Human 260 Genes GS232040: PC Geneset - "V$E2A_Q2" pathway genes
Expand Tier I Human 621 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier II Human 12085 Genes GS240544: [MeSH] Pregnancy : D011247
Expand Tier II Human 242 Genes GS239799: [MeSH] Leukopenia : D007970
Expand Tier I Human 356 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier II Human 83226 Genes GS241072: [MeSH] Genetic Phenomena : D055614
Expand Tier II Human 60093 Genes GS243325: [MeSH] Base Sequence : D001483
Expand Tier I Human 102 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Mouse 573 Genes GS136920: vertebral morphology and mechanical traits 8 (Vmmt8, Published QTL Chr 8)
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse 849 Genes GS128577: Ethanol induced LORR Chr# 8
Expand Tier I Human 53 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier II Human 20421 Genes GS237820: [MeSH] DNA Primers : D017931
Expand Tier I Mouse 200 Genes GS227730: MSigDB Geneset - GSE17721_12H_VS_24H_PAM3CSK4_BMDM_UP
Expand Tier II Human 24024 Genes GS240200: [MeSH] Transcription Initiation Site : D024363
Expand Tier I Mouse 460 Genes GS135886: forelimb polydactyly (Fpdty, Published QTL Chr 8)
Expand Tier I Human 269 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier II Human 23569 Genes GS235276: [MeSH] Signal Transduction : D015398
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
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 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier II Human 1212 Genes GS237751: [MeSH] Phosphoric Diester Hydrolases : D010727
Expand Tier I Human 79 Genes GS171446: HP:0000600 Abnormality of the pharynx
Expand Tier I Human GO 2331 Genes GS208037: GO:0016787 hydrolase activity
Expand Tier II Human 12369 Genes GS245348: [MeSH] RNA Processing, Post-Transcriptional : D012323
Expand Tier II Human 452 Genes GS236254: [MeSH] RNA, Nuclear : D015138
Expand Tier I Human 15 Genes GS176419: HP:0100670 Rough bone trabeculation
Expand Tier II Human 4291 Genes GS236727: [MeSH] Skin and Connective Tissue Diseases : D017437
Expand Tier I Human 85 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier II Human 13237 Genes GS241118: [MeSH] Binding Sites : D001665
Expand Tier I Human 69 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier I Human GO 204 Genes GS210307: GO:0034470 ncRNA processing
Expand Tier III Rat 526 Genes GS223517: Plasma insulin-like growth factor 1 level QTL 10 (Pigfal10 Published QTL Chr 19)
Expand Tier I Mouse 568 Genes GS136512: prion incubation time 3 (Pitm3, Published QTL Chr 8)
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier II Human 73736 Genes GS238575: [MeSH] Nucleic Acids : D009696
Expand Tier I Mouse 589 Genes GS135717: despair 1 (Desp1, Published QTL Chr 8)
Expand Tier I Human 196 Genes GS228760: MSigDB Geneset - GSE37416_12H_VS_48H_F_TULARENSIS_LVS_NEUTROPHIL_UP
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 196 Genes GS229065: MSigDB Geneset - GSE3982_BCELL_VS_NKCELL_DN
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 19 Genes GS175796: HP:0002894 Neoplasm of the pancreas
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier III Rat 592 Genes GS223520: Tongue tumor susceptibility QTL 1 (Tcas1 Published QTL Chr 19)
Expand Tier II Human 22498 Genes GS245206: [MeSH] Cell Nucleus : D002467
Expand Tier I Human 119 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier II Human 18755 Genes GS242691: [MeSH] Embryonic Structures : D004628
Expand Tier I Mouse 573 Genes GS135844: femoral cross-sectional area 2 (Fcsa2, Published QTL Chr 8)
Expand Tier I Human 93 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse 574 Genes GS136369: obesity QTL 16 (Obq16, Published QTL Chr 8)
Expand Tier I Mouse 200 Genes GS230436: MSigDB Geneset - GSE17721_POLYIC_VS_PAM3CSK4_6H_BMDM_UP
Expand Tier I Human 194 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier II Human 58261 Genes GS239502: [MeSH] Nucleic Acid Probes : D015341
Expand Tier II Human 314 Genes GS240134: [MeSH] DNA Repair-Deficiency Disorders : D049914
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Mouse GO 23849 Genes GS180164: GO:0008150 biological_process
Expand Tier II Human 30111 Genes GS244835: [MeSH] Chromosomes : D002875
Expand Tier I Mouse 586 Genes GS136300: mean platelet volume locus 2 (Mpvq2, Published QTL Chr 8)
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 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Mouse GO 6435 Genes GS177531: GO:0043170 macromolecule metabolic process
Expand Tier I Human 136 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 45 Genes GS171845: HP:0008066 Abnormal blistering of the skin
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier II Human 52165 Genes GS242059: [MeSH] Cells : D002477
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
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 Mouse GO 3978 Genes GS188506: GO:0010467 gene expression
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse 460 Genes GS136131: lithogenic gene 11 (Lith11, Published QTL Chr 8)
Expand Tier I Mouse 456 Genes GS136733: susceptibility to lung cancer 9 (Sluc9, Published QTL Chr 8)
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier II Human 58105 Genes GS235797: [MeSH] DNA Probes : D015342
Expand Tier II Human 29719 Genes GS237296: [MeSH] RNA, Antisense : D016372
Expand Tier I Human GO 159 Genes GS208951: GO:0004518 nuclease activity
Expand Tier I Mouse 445 Genes GS135466: blood pressure QTL 23 (Bpq23, Published QTL Chr 8)
Expand Tier I Mouse 528 Genes GS136355: novelty/stress induced locomotor activation 6 (Nsila6, Published QTL Chr 8)
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human GO 404 Genes GS197735: GO:0006397 mRNA processing
Expand Tier II Human 30298 Genes GS242332: [MeSH] Cell Physiological Phenomena : D002468
Expand Tier I Human 197 Genes GS227211: MSigDB Geneset - GSE29617_CTRL_VS_DAY3_TIV_FLU_VACCINE_PBMC_2008_DN
Expand Tier II Human 41481 Genes GS234192: [MeSH] Gene Expression Regulation : D005786
Expand Tier II Human 58023 Genes GS235242: [MeSH] Biochemical Processes : D055438
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse 200 Genes GS230557: MSigDB Geneset - GSE17721_12H_VS_24H_POLYIC_BMDM_UP
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier II Human 52588 Genes GS245685: [MeSH] RNA : D012313
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier II Human 12397 Genes GS235736: [MeSH] DNA Transposable Elements : D004251
Expand Tier I Human 149 Genes GS230458: MSigDB Geneset - GCCNNNWTAAR_UNKNOWN
Expand Tier I Mouse 200 Genes GS230694: MSigDB Geneset - GSE17721_PAM3CSK4_VS_GADIQUIMOD_6H_BMDM_DN
Expand Tier II Human 20860 Genes GS239302: [MeSH] Oligonucleotides : D009841
Expand Tier I Mouse 519 Genes GS135589: P. chabaudi malaria resistance QTL 2 (Char2, Published QTL Chr 8)
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 122 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier III Rat 558 Genes GS223524: Tongue tumor susceptibility QTL 5 (Tcas5 Published QTL Chr 19)
Expand Tier II Human 28877 Genes GS238592: [MeSH] Cells, Cultured : D002478
Expand Tier I Human 95 Genes GS176759: HP:0000982 Palmoplantar keratoderma
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 Mouse GO 4651 Genes GS177310: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 2919 Genes GS229203: MSigDB Geneset - GGGCGGR_V$SP1_Q6
Expand Tier I Human 194 Genes GS227273: MSigDB Geneset - GSE7400_CTRL_VS_CSF3_IN_VIVO_TREATED_PBMC_DN
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse 199 Genes GS228064: MSigDB Geneset - GSE17721_LPS_VS_GARDIQUIMOD_16H_BMDM_UP
Expand Tier II Human 947 Genes GS240287: [MeSH] Telomere : D016615
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Mouse GO 5 Genes GS191908: GO:0043628 ncRNA 3'-end processing
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier III Rat 404 Genes GS224364: Cardiac mass QTL 12 (Cm12 Published QTL Chr 19)
Expand Tier II Human 15731 Genes GS236183: [MeSH] Chromosome Structures : D022004
Expand Tier II Human 896 Genes GS236992: [MeSH] Chromosomes, Human, 16-18 : D002902
Expand Tier I Human 1157 Genes GS228342: MSigDB Geneset - GATTGGY_V$NFY_Q6_01
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 146 Genes GS173537: HP:0001872 Abnormality of thrombocytes
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 Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier II Human 12283 Genes GS244576: [MeSH] Genome, Insect : D049750
Expand Tier I Human GO 731 Genes GS208043: GO:0016788 hydrolase activity, acting on ester bonds
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 200 Genes GS229782: MSigDB Geneset - GSE1432_6H_VS_24H_IFNG_MICROGLIA_UP
Expand Tier I Mouse GO 2 Genes GS182584: GO:0034472 snRNA 3'-end processing
Expand Tier II Human 58901 Genes GS243233: [MeSH] Specialty Uses of Chemicals : D020313
Expand Tier I Human 114 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Mouse GO 3136 Genes GS187045: GO:0016070 RNA metabolic process
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier II Human 3803 Genes GS243242: [MeSH] Skin Diseases : D012871
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 44 Genes GS176540: HP:0002721 Immunodeficiency
Expand Tier I Human 213 Genes GS176973: HP:0001072 Thickened skin
Expand Tier II Human 15607 Genes GS241444: [MeSH] Reproductive Physiological Phenomena : D055703
Expand Tier I Human 50 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Mouse 444 Genes GS136390: autoimmune orchitis resistance 6 (Orch6, Published QTL Chr 8)
Expand Tier II Human 36882 Genes GS236241: [MeSH] Protein Structure, Tertiary : D017434
Expand Tier I Human 79 Genes GS172887: HP:0100533 Inflammatory abnormality of the eye
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier II Human 14570 Genes GS237160: [MeSH] Repetitive Sequences, Nucleic Acid : D012091
Expand Tier I Human 189 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human GO 16 Genes GS203911: GO:0016073 snRNA metabolic process
Expand Tier II Human 21049 Genes GS244735: [MeSH] Mutagenesis : D016296
Expand Tier I Human 49 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 51 Genes GS174291: HP:0002575 Tracheoesophageal fistula
Expand Tier I Human 307 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier II Human 5871 Genes GS237484: [MeSH] Congenital, Hereditary, and Neonatal Diseases and Abnormalities : D009358
Expand Tier I Mouse 747 Genes GS129101: bone mineral density 39 (Bmd39 Published QTL Chr 8)
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier II Human 73356 Genes GS238415: [MeSH] Genome Components : D040481
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier II Human 1323 Genes GS243817: [MeSH] Abnormalities, Multiple : D000015
Expand Tier I Human 85 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier I Human 34 Genes GS173892: HP:0005528 Bone marrow hypocellularity
Expand Tier I Human 240 Genes GS229640: MSigDB Geneset - V$E2A_Q2
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse 444 Genes GS135780: exercise endurance QTL 2 (Eeq2, Published QTL Chr 8)
Expand Tier II Human 39556 Genes GS238930: [MeSH] Molecular Conformation : D008968
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 II Human 4244 Genes