Gene Details



NOP10 and homologs in 5 species are found in 356 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 131 Genes GS175744: HP:0001231 Abnormality of the fingernails
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse 643 Genes GS135594: mean cell hemoglobin concentration QTL 1 (Chcmq1, Published QTL Chr 2)
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse 451 Genes GS135564: cytokine deficiency colitis susceptibility 3 (Cdcs3, Published QTL Chr 2)
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse 690 Genes GS136114: body length 1 (Lgth1, Published QTL Chr 2)
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Mouse GO 141 Genes GS190626: GO:0042254 ribosome biogenesis
Expand Tier III Mouse 460 Genes GS836: Differential expression in Sey Pax6 mutants and controls. Additive effect of mutation, linear increase in both mutants and Wild-types.
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 103 Genes GS174372: HP:0002024 Malabsorption
Expand Tier I Human 322 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Mouse 1196 Genes GS129192: type 2 diabetes mellitus 2 in SMXA RI mice (T2dm2sa Published QTL Chr 2)
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 111 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier III Human 735 Genes GS1229: Differential gene expression among both the Heroin and Cocaine Abusers
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 3 Genes GS176779: HP:0010450 Esophageal stenosis
Expand Tier I Human 34 Genes GS174840: HP:0011358 Generalized hypopigmentation of hair
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human 285 Genes GS171902: HP:0010987 Abnormality of cellular immune system
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 56 Genes GS174818: HP:0007495 Prematurely aged appearance
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 4619 Genes GS191019: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human 120 Genes GS170783: HP:0010974 Abnormality of myeloid leukocytes
Expand Tier I Human 44 Genes GS174484: HP:0000521 Abnormality of tear glands or tear production
Expand Tier I Mouse GO 1464 Genes GS182313: GO:0044085 cellular component biogenesis
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 47 Genes GS199228: GO:0015030 Cajal body
Expand Tier I Human 189 Genes GS172471: HP:0001744 Splenomegaly
Expand Tier I Human 125 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Mouse 448 Genes GS135237: activity response to ethanol 4 (Actre4, Published QTL Chr 2)
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 4353 Genes GS192017: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Mouse 469 Genes GS136403: organ weight QTL 3 (Orgwq3, Published QTL Chr 2)
Expand Tier I Human 1223 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 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 38 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 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Mouse 559 Genes GS135670: circadian period of locomotor activity 7 (Cplaq7, Published QTL Chr 2)
Expand Tier I Human 592 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 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Mouse GO 524 Genes GS180942: GO:0006396 RNA processing
Expand Tier I Mouse 621 Genes GS136639: salmonella enteritidis susceptibility 7 (Ses7, Published QTL Chr 2)
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
Expand Tier I Mouse 708 Genes GS136735: segregation of mitochondrial DNA QTL 2 (Smdq2, Published QTL Chr 2)
Expand Tier I Mouse 482 Genes GS135219: aberrant activation of B cell proliferation (Aabpr, Published QTL Chr 2)
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 184 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human 14 Genes GS173377: HP:0002209 Sparse scalp hair
Expand Tier I Mouse 552 Genes GS136115: body length 2 (Lgth2, Published QTL Chr 2)
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier II Mouse 554 Genes GS84133: activity response to ethanol (Published QTL, Chr 2)
Expand Tier I Human 81 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Human 20 Genes GS176420: HP:0100671 Abnormal trabecular bone morphology
Expand Tier I Human GO 273 Genes GS202843: GO:0016604 nuclear body
Expand Tier I Human 21 Genes GS173273: HP:0002216 Premature graying of hair
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 16 Genes GS172127: HP:0000632 Lacrimation abnormality
Expand Tier I Human 187 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 78 Genes GS173155: HP:0005561 Abnormality of bone marrow cell morphology
Expand Tier I Mouse 471 Genes GS135685: C. trachomatis resistance QTL 1 (Ctrq1, Published QTL Chr 2)
Expand Tier I Mouse 622 Genes GS136950: weight gain in high growth mice 5 (Wg5, Published QTL Chr 2)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 223 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human 57 Genes GS176765: HP:0001009 Telangiectasia
Expand Tier I Human 56 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Mouse 585 Genes GS136377: obesity QTL 3 (Obq3, Published QTL Chr 2)
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 90 Genes GS173087: HP:0000499 Abnormality of the eyelashes
Expand Tier I Mouse 568 Genes GS136872: T cell ratio modifier QTL 2 (Trmq2, Published QTL Chr 2)
Expand Tier I Human 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 115 Genes GS171171: HP:0005607 Abnormality of the tracheobronchial system
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 26 Genes GS175546: HP:0010885 Aseptic necrosis
Expand Tier I Human 50 Genes GS176640: HP:0011357 Abnormality of hair density
Expand Tier I Human GO 229 Genes GS200149: GO:0022613 ribonucleoprotein complex biogenesis
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 623 Genes GS196553: GO:0005730 nucleolus
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 151 Genes GS207521: GO:0042254 ribosome biogenesis
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human 41 Genes GS172655: HP:0001792 Small nail
Expand Tier I Mouse GO 192 Genes GS193365: GO:0034470 ncRNA processing
Expand Tier I Human DRG 911 Genes provisional GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG]
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human 102 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Mouse 690 Genes GS136090: lean body mass 2 (Lbm2, Published QTL Chr 2)
Expand Tier I Mouse GO 247 Genes GS182492: GO:0034660 ncRNA metabolic process
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 208 Genes GS178358: GO:0071843 cellular component biogenesis at cellular level
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Mouse 559 Genes GS135694: directional asymmetry QTL 18 (Daq18, Published QTL Chr 2)
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier III Mouse 6105 Genes GS213074: Genes with suggestive difference in (B6PF1) vs (PB6F1 + B6 + PWD) comparison
Expand Tier I Human 57 Genes GS174179: HP:0002514 Cerebral calcification
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Mouse 552 Genes GS135795: ethanol induced low dose activation 3 (Elda3, Published QTL Chr 2)
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 79 Genes GS173387: HP:0002757 Recurrent fractures
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 25 Genes GS173554: HP:0005374 Cellular immunodeficiency
Expand Tier I Human GO 56 Genes GS206092: GO:0009451 RNA modification
Expand Tier I Mouse 451 Genes GS135918: graft-versus host disease 3 (Gvhd3, Published QTL Chr 2)
Expand Tier I Human 83 Genes GS171602: HP:0001965 Abnormality of the scalp
Expand Tier I Human 4 Genes GS174030: HP:0009926 Increased lacrimation
Expand Tier I Human 77 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 129 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier II Mouse 580 Genes GS84131: ethanol consumption (Published QTL, Chr 2)
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 244 Genes GS195111: GO:0071843 cellular component biogenesis at cellular level
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 289 Genes GS199289: GO:0034660 ncRNA metabolic process
Expand Tier I Human 26 Genes GS172624: HP:0000653 Sparse eyelashes
Expand Tier I Human 33 Genes GS173533: HP:0001876 Pancytopenia
Expand Tier I Human 266 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 111 Genes GS175068: HP:0000971 Abnormality of the sweat gland
Expand Tier I Human 285 Genes GS175119: HP:0001881 Abnormality of leukocytes
Expand Tier I Human 174 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 177 Genes GS173540: HP:0002115 Sparse or absent hair
Expand Tier I Human 46 Genes GS175084: HP:0008384 Aplastic/hypoplastic fingernail
Expand Tier I Human 49 Genes GS176790: HP:0008070 Sparse hair
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Mouse 552 Genes GS136472: periosteal circumference and femur length 2 (Pcfm2, Published QTL Chr 2)
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 80 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Human GO 553 Genes GS207972: GO:0030529 ribonucleoprotein complex
Expand Tier I Mouse 469 Genes GS136445: peripheral blood stem cell response to granulocyte colony stimulating factor 1 (Pbrgcsf1, Published QTL Chr 2)
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Tier I Mouse 552 Genes GS136011: heart rate quantitative locus 1 (Hrq1, Published QTL Chr 2)
Expand Tier I Human GO 1477 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 67 Genes GS171788: HP:0001394 Cirrhosis
Expand Tier I Mouse 3115 Genes GS128575: Ethanol induced LORR Chr# 2
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Mouse 552 Genes GS136600: serum alkaline phosphatase activity 1 (Salpa1, Published QTL Chr 2)
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human GO 2673 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Mouse 742 Genes GS129195: Tmc1 modifier 1 (Tmc1m1 Published QTL Chr 2)
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 95 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 40 Genes GS171916: HP:0002665 Lymphoma
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 655 Genes GS197734: GO:0006396 RNA processing
Expand Tier I Human 23 Genes GS173296: HP:0011830 Abnormality of oral mucosa
Expand Tier I Human 79 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse 1157 Genes GS129156: multigenic obesity QTL 5 (Mobq5 Published QTL Chr 2)
Expand Tier I Human 102 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 6 Genes GS176842: HP:0001915 Aplastic anemia
Expand Tier I Mouse 547 Genes GS136364: obesity QTL 10 (Obq10, Published QTL Chr 2)
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse GO 193 Genes GS183353: GO:0022613 ribonucleoprotein complex biogenesis
Expand Tier I Mouse 450 Genes GS135855: femoral bone morphometry 4 (Fembm4, Published QTL Chr 2)
Expand Tier I Mouse 560 Genes GS136160: leishmaniasis resistance 14 (Lmr14, Published QTL Chr 2)
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse DRG 2537 Genes provisional GS86906: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). Lists of probe sets and gene names altered by strain (3457). [DRG]
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Mouse 625 Genes GS135837: total fat pad mass QTL 1 (Fatmq1, Published QTL Chr 2)
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human 55 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 80 Genes GS171446: HP:0000600 Abnormality of the pharynx
Expand Tier I Human 16 Genes GS176419: HP:0100670 Rough bone trabeculation
Expand Tier I Human 86 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Human 70 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier I Human GO 204 Genes GS210307: GO:0034470 ncRNA processing
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse 450 Genes GS135892: failure of ureteric bud invasion 1 (Fubi1, Published QTL Chr 2)
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse 791 Genes GS129169: plasma plant sterol 2b (Plast2b Published QTL Chr 2)
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 20 Genes GS175796: HP:0002894 Neoplasm of the pancreas
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse 556 Genes GS135584: cholesterol absorption 1 (Chab1, Published QTL Chr 2)
Expand Tier I Human 121 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human 94 Genes GS174190: HP:0001596 Alopecia
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse GO 2872 Genes GS178360: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 196 Genes GS173872: HP:0011368 Epidermal thickening
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human GO 13 Genes GS195911: GO:0005732 small nucleolar ribonucleoprotein complex
Expand Tier I Mouse GO 99 Genes GS177212: GO:0006364 rRNA processing
Expand Tier I Human 922 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 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 46 Genes GS171845: HP:0008066 Abnormal blistering of the skin
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Mouse GO 3583 Genes GS180236: GO:0032991 macromolecular complex
Expand Tier I Mouse 617 Genes GS136527: prion disease incubation time 1 (Prdt1, Published QTL Chr 2)
Expand Tier I Human 474 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 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Mouse GO 563 Genes GS191064: GO:0030529 ribonucleoprotein complex
Expand Tier I Mouse DRG 2693 Genes GS87380: Table S1: Additional data file 1 is a table listing the results of two-way ANOVA (FDR < 1%). (Whole Table) [DRG]
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Mouse 559 Genes GS136595: rotarod performance 2 (Rrodp2, Published QTL Chr 2)
Expand Tier I Human 14 Genes GS171660: HP:0000614 Abnormality of the nasolacrimal system
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Mouse 534 Genes GS135235: activity response to ethanol 2 (Actre2, Published QTL Chr 2)
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human 3 Genes GS174785: HP:0002043 Esophageal stricture
Expand Tier I Mouse 736 Genes GS136914: vertebral morphology and mechanical traits 2 (Vmmt2, Published QTL Chr 2)
Expand Tier I Mouse 501 Genes GS136873: T cell ratio modifier QTL 3 (Trmq3, Published QTL Chr 2)
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human 2 Genes GS170823: HP:0002165 Pterygium formation (nails)
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 124 Genes GS172403: HP:0011873 Abnormal platelet count
Expand Tier I Human 232 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human 96 Genes GS176759: HP:0000982 Palmoplantar keratoderma
Expand Tier I Mouse 555 Genes GS136360: Neuroadapted Sindbis viral RNA level 1 (Nsv1, Published QTL Chr 2)
Expand Tier I Human 545 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1569 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 II Mouse 613 Genes GS84132: ethanol induced locomotor activity (Published QTL, Chr 2)
Expand Tier I Human 9 Genes GS173616: HP:0002745 Oral leukoplakia
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Mouse 631 Genes GS136010: hemotopoietic response to early cytokines (Hrec, Published QTL Chr 2)
Expand Tier I Mouse GO 103 Genes GS187047: GO:0016072 rRNA metabolic process
Expand Tier I Mouse 450 Genes GS136055: IgA nephropathy QTL 1 (Ignpq1, Published QTL Chr 2)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Human GO 3861 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 489 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human 10 Genes GS175118: HP:0000579 Nasolacrimal duct obstruction
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier III Mouse 8107 Genes GS213076: Genes with suggestive difference in (B6) vs (B6PF1 + PB6F1 + PWD) comparison
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 110 Genes GS203910: GO:0016072 rRNA metabolic process
Expand Tier I Human 50 Genes GS173561: HP:0000691 Microdontia
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Mouse GO 3136 Genes GS187045: GO:0016070 RNA metabolic process
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Mouse 610 Genes GS135704: diabetes mRNA cluster 1 (Dbmc1, Published QTL Chr 2)
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 73 Genes GS170824: HP:0002164 Nail dysplasia
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 46 Genes GS176540: HP:0002721 Immunodeficiency
Expand Tier I Human 215 Genes GS176973: HP:0001072 Thickened skin
Expand Tier I Human 52 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Human 80 Genes GS172887: HP:0100533 Inflammatory abnormality of the eye
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Mouse 451 Genes GS135858: femur breaking strength 1 (Fembrs1, Published QTL Chr 2)
Expand Tier I Mouse 467 Genes GS136105: lymph node cytotoxic T lymphocyte percentage 1 (Lctlp1, Published QTL Chr 2)
Expand Tier I Mouse 451 Genes GS136797: total body bone mineral density 2 (Tbbmd2, Published QTL Chr 2)
Expand Tier I Human 50 Genes GS174380: HP:0010624 Aplastic/hypoplastic toenails
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse 683 Genes GS135418: bitterness sensitivity 1 (Bits1, Published QTL Chr 2)
Expand Tier I Mouse 622 Genes GS135708: diabetes susceptibility QTL 5 (Dbsq5, Published QTL Chr 2)
Expand Tier I Human 12 Genes GS175372: HP:0011481 Abnormality of the lacrimal duct
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Mouse 736 Genes GS135554: CD8 memory T cell subset 3 (Cd8mts3, Published QTL Chr 2)
Expand Tier I Human GO 104 Genes GS193935: GO:0006364 rRNA processing
Expand Tier I Human 52 Genes GS174291: HP:0002575 Tracheoesophageal fistula
Expand Tier I Human 310 Genes GS175805: HP:0003271 Visceromegaly
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 87 Genes GS173838: HP:0002778 Abnormality of the trachea
Expand Tier I Human 36 Genes GS173892: HP:0005528 Bone marrow hypocellularity
Expand Tier I Human GO 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 17 Genes GS205822: GO:0001522 pseudouridine synthesis