Gene Details



WRAP53 and homologs in 4 species are found in 402 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 Mouse 763 Genes GS135990: Hfe modifier 3 (Hfem3, Published QTL Chr 11)
Expand Tier I Human GO 853 Genes GS203097: GO:0003723 RNA binding
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 1047 Genes GS135864: femur length in high growth mice 4 (Feml4, Published QTL Chr 11)
Expand Tier I Mouse 1061 Genes GS136647: serum IGFBP-5 level QTL 6 (Si5lq6, Published QTL Chr 11)
Expand Tier I Mouse 850 Genes GS135637: cytokine induced activation 1 (Cinda1, Published QTL Chr 11)
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Mouse 996 Genes GS136853: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 5 (Tmevd5, Published QTL Chr 11)
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 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 Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Mouse 990 Genes GS136605: spinal bone mineral density 4 (Sbmd4, Published QTL Chr 11)
Expand Tier I Human 111 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Mouse 763 Genes GS136658: skeletal muscle weight 17 (Skmw17, Published QTL Chr 11)
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse GO 4887 Genes GS188190: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 3 Genes GS209795: GO:0032203 telomere formation via telomerase
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Mouse 595 Genes GS129171: pregnancy QTL 1 (Pregq1 Published QTL Chr 11)
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 Mouse 870 Genes GS136432: pulmonary adenoma susceptibility 5 (Pas5, Published QTL Chr 11)
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 Mouse 1061 Genes GS136798: total body bone mineral density 5 (Tbbmd5, Published QTL Chr 11)
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 Mouse 1061 Genes GS136208: liver weight QTL 9 (Lwq9, Published QTL Chr 11)
Expand Tier II Mouse 835 Genes GS84252: alcohol preference locus (Published QTL, Chr 11)
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 Mouse GO 10 Genes GS186536: GO:0051972 regulation of telomerase activity
Expand Tier I Mouse GO 1464 Genes GS182313: GO:0044085 cellular component biogenesis
Expand Tier I Mouse GO 1870 Genes GS192986: GO:0006996 organelle organization
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse GO 727 Genes GS179950: GO:0006259 DNA metabolic process
Expand Tier I Human GO 47 Genes GS199228: GO:0015030 Cajal body
Expand Tier III Fly 2671 Genes GS213271: Head and thorax heatmapping of Canton-S fruit flies with dietary restrictions
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 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 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 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Mouse GO 3493 Genes GS177570: GO:0016043 cellular component organization
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 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 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Mouse 1008 Genes GS136767: streptozotocin induced diabetes susceptibility (Stzid, Published QTL Chr 11)
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Mouse 590 Genes GS136646: serum IGFBP-5 level QTL 5 (Si5lq5, Published QTL Chr 11)
Expand Tier I Mouse 609 Genes GS135718: despair 2 (Desp2, Published QTL Chr 11)
Expand Tier I Human 114 Genes GS176840: HP:0001911 Abnormality of granulocytes
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 Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
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 III Fly 2674 Genes GS213272: Head and thorax heatmapping of reservatrol treated Canton-S fruit flies
Expand Tier I Mouse 988 Genes GS136696: systematic lupus erythematosus susceptibility 13 (Sle13, Published QTL Chr 11)
Expand Tier I Mouse 885 Genes GS136294: modifier of Trp53 1 (Motp1, Published QTL Chr 11)
Expand Tier I Mouse 988 Genes GS136481: plasmacytoma susceptibility 3 (Pcyts3, Published QTL Chr 11)
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse 869 Genes GS136581: red blood cell QTL 3 (Rbcq3, Published QTL Chr 11)
Expand Tier I Human CTD 1453 Genes GS121893: Vitamin E interacting genes (MeSH:D014810) in CTD
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 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 20 Genes GS176420: HP:0100671 Abnormal trabecular bone morphology
Expand Tier I Human GO 688 Genes GS193888: GO:0051276 chromosome organization
Expand Tier I Human GO 64 Genes GS201554: GO:0032200 telomere organization
Expand Tier I Human 246 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Mouse 1047 Genes GS136901: ventral midbrain iron content 6 (Vmbic6, Published QTL Chr 11)
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 870 Genes GS136877: tooth shape 10 (Tshp10, Published QTL Chr 11)
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 GO 1332 Genes GS189748: GO:0050790 regulation of catalytic activity
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Mouse GO 513 Genes GS178810: GO:0051338 regulation of transferase activity
Expand Tier I Human 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 26 Genes GS175546: HP:0010885 Aseptic necrosis
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
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 Mouse 765 Genes GS136325: non-insulin-dependent diabetes mellitus 1 in NSY (Nidd1n, Published QTL Chr 11)
Expand Tier I Mouse 763 Genes GS135793: ethanol induced low dose activation 1 (Elda1, Published QTL Chr 11)
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 Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier II Mouse 36 Genes GS34085: Striatum Gene expression correlates of Open Field rears 45-60 min post cocaine in Females BXD
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier III Mouse 8003 Genes GS213041: Expression profiles of aging in C57BL/6 mouse hippocampal tissue
Expand Tier I Human GO 1087 Genes GS203482: GO:0044093 positive regulation of molecular function
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 GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 25 Genes GS173554: HP:0005374 Cellular immunodeficiency
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
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 Mouse GO 488 Genes GS179789: GO:0005730 nucleolus
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 GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Mouse 850 Genes GS135966: HDL QTL 37 (Hdlq37, Published QTL Chr 11)
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 80 Genes GS175083: HP:0008386 Aplasia/Hypoplasia of the nails
Expand Tier I Human GO 5 Genes GS197245: GO:0032202 telomere assembly
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
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 1061 Genes GS136119: body length 6 (Lgth6, Published QTL Chr 11)
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 Mouse GO 8942 Genes GS185492: GO:0050789 regulation of biological process
Expand Tier I Mouse 1061 Genes GS136528: prion disease incubation time 3 (Prdt3, Published QTL Chr 11)
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 GO 10879 Genes GS181473: GO:0005488 binding
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 1777 Genes GS184445: GO:0044428 nuclear part
Expand Tier I Human 95 Genes GS176573: HP:0008065 Aplasia/Hypoplasia of the skin
Expand Tier I Mouse 1068 Genes GS136388: autoimmune orchitis resistance 3 (Orch3, Published QTL Chr 11)
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 79 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Human 102 Genes GS172692: HP:0002659 Increased susceptibility to fractures
Expand Tier I Human GO 653 Genes GS195566: GO:0051338 regulation of transferase activity
Expand Tier I Mouse GO 780 Genes GS186251: GO:0003723 RNA binding
Expand Tier I Mouse 1281 Genes GS129115: collagen induced arthritis 40 (Cia40 Published QTL Chr 11)
Expand Tier I Human 266 Genes GS172415: HP:0002240 Hepatomegaly
Expand Tier I Mouse GO 5 Genes GS183654: GO:0051973 positive regulation of telomerase activity
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Mouse 870 Genes GS135519: body weight at necropsy 3 (Bwtn3, Published QTL Chr 11)
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier III Rat 3441 Genes GS135132: bHR vs bLR genes different in Nucleus Acumbens
Expand Tier I Human 104 Genes GS173535: HP:0001874 Abnormality of neutrophils
Expand Tier I Human 55 Genes GS171305: HP:0012145 Abnormality of multiple cell lineages in the bone marrow
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier III Rat 3441 Genes GS135133: bHR vs bLR genes different in Hippocampus
Expand Tier I Human 16 Genes GS176419: HP:0100670 Rough bone trabeculation
Expand Tier I Human 70 Genes GS175064: HP:0000975 Hyperhidrosis
Expand Tier III Mouse 8392 Genes GS128199: Alcohol Preference union of 86 Gene Sets
Expand Tier I Mouse 848 Genes GS135868: fat induced adiposity 1 (Fina1, Published QTL Chr 11)
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Mouse 1061 Genes GS136477: periosteal circumference 2 (Pcir2, Published QTL Chr 11)
Expand Tier I Human 20 Genes GS175796: HP:0002894 Neoplasm of the pancreas
Expand Tier I Human 94 Genes GS174190: HP:0001596 Alopecia
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 Mouse GO 1582 Genes GS188684: GO:0070013 intracellular organelle lumen
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
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 Mouse 761 Genes GS135686: C. trachomatis resistance QTL 3 (Ctrq3, Published QTL Chr 11)
Expand Tier I Mouse GO 5 Genes GS180453: GO:0032202 telomere assembly
Expand Tier I Mouse GO 1587 Genes GS182475: GO:0043233 organelle lumen
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Mouse 999 Genes GS135823: ethanol conditioned taste aversion 9 (Etohcta9, Published QTL Chr 11)
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 1004 Genes GS135766: experimental allergic encephalomyelitis susceptibility 7 (Eae7, Published QTL Chr 11)
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 770 Genes GS136444: peak bone mineral density 4 (Pbmd4, Published QTL Chr 11)
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 Human GO 895 Genes GS200867: GO:0043085 positive regulation of catalytic activity
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Mouse GO 1381 Genes GS192610: GO:0031981 nuclear lumen
Expand Tier I Mouse GO 4478 Genes GS184435: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 6 Genes GS202777: GO:0005697 telomerase holoenzyme complex
Expand Tier I Mouse GO 24 Genes GS182431: GO:0015030 Cajal body
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
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 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 I Mouse 998 Genes GS136543: periosteal circumference 2 (Pstc2, Published QTL Chr 11)
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1544 Genes GS195733: GO:0022607 cellular component assembly
Expand Tier I Mouse 762 Genes GS136864: T cell receptor induced activation 1 (Tria1, Published QTL Chr 11)
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Mouse 1071 Genes GS135702: dopamine uptake transporter binding 4 (Dautb4, Published QTL Chr 11)
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 Mouse GO 2876 Genes GS182474: GO:0043232 intracellular non-membrane-bounded organelle
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 Mouse 848 Genes GS135593: P. chabaudi malaria resistance QTL 8 (Char8, Published QTL Chr 11)
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 148 Genes GS173537: HP:0001872 Abnormality of thrombocytes
Expand Tier I Mouse 848 Genes GS136907: vertebral morphology and mechanical traits 12 (Vmmt12, Published QTL Chr 11)
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 Mouse 848 Genes GS136161: leishmaniasis resistance 15 (Lmr15, Published QTL Chr 11)
Expand Tier I Human 115 Genes GS172500: HP:0007400 Irregular hyperpigmentation
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse 988 Genes GS136337: nicotine induced locomotor activity 2 (Nilac2, Published QTL Chr 11)
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 7336 Genes GS201431: GO:0005515 protein binding
Expand Tier I Mouse 1039 Genes GS136708: semilethal sex-restricted (Slthsr, Published QTL Chr 11)
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 III Mouse 629 Genes GS37187: Positional candidate on chromosome 11 (59-79Mb) for overdominant effect for 24-hour, 2 bottle choice 30g/kg EtOH excessive consumption.
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 GO 1799 Genes GS196933: GO:0065009 regulation of molecular function
Expand Tier I Human 52 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Human 107 Genes GS176569: HP:0008069 Neoplasm of the skin
Expand Tier I Mouse 1061 Genes GS136560: QTL for body weight independent of sex 3 (Qbis3, Published QTL Chr 11)
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 Mouse 1061 Genes GS136086: kidney weight QTL 15 (Kwq15, Published QTL Chr 11)
Expand Tier I Mouse GO 610 Genes GS177169: GO:0051276 chromosome organization
Expand Tier I Mouse 340 Genes GS129152: immunity to S. typhimurium 2b (Ity2b Published QTL Chr 11)
Expand Tier I Human 192 Genes GS174579: HP:0002031 Abnormality of the esophagus
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse GO 4224 Genes GS193059: GO:0044446 intracellular organelle part
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 799 Genes GS136611: colon tumor susceptibility 15 (Scc15, Published QTL Chr 11)
Expand Tier I Mouse 999 Genes GS136048: insulin dependent diabetes susceptibility 4 (Idd4, Published QTL Chr 11)
Expand Tier I Human GO 1425 Genes GS206620: GO:0050790 regulation of catalytic activity
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
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 Mouse 848 Genes GS135430: bone mineral density 11 (Bmd11, Published QTL Chr 11)
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Mouse 885 Genes GS136502: proteoglycan induced arthritis 7 (Pgia7, Published QTL Chr 11)
Expand Tier I Mouse 856 Genes GS135919: graft-versus host disease 4 (Gvhd4, Published QTL Chr 11)
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 Mouse GO 681 Genes GS184065: GO:0043085 positive regulation of catalytic activity
Expand Tier I Mouse 1077 Genes GS135507: body weight QTL 4 (Bw4, Published QTL Chr 11)
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 5 Genes GS200455: GO:0051973 positive regulation of telomerase activity
Expand Tier I Human 15 Genes GS174120: HP:0002860 Squamous cell carcinoma
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Mouse 988 Genes GS136566: retinoic acid induced forelimb autopod reduction (Rafar, Published QTL Chr 11)
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 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Mouse GO 9323 Genes GS180152: GO:0065007 biological regulation
Expand Tier I Mouse 768 Genes GS136219: mandible length 11 (Manln11, Published QTL Chr 11)
Expand Tier I Mouse 861 Genes GS136302: modifier of Salmonella typhimurium susceptibility 3 (Msts3, Published QTL Chr 11)
Expand Tier I Mouse 1077 Genes GS135366: B.burgdorferi-associated arthritis 4 (Bbaa4, Published QTL Chr 11)
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Mouse GO 169 Genes GS186007: GO:0016604 nuclear body
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 258 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Mouse 883 Genes GS128596: Change in rotarod latency over training trials Chr#11
Expand Tier I Mouse 1142 Genes GS129196: Tmc1 modifier 2 (Tmc1m2 Published QTL Chr 11)
Expand Tier I Human GO 623 Genes GS196553: GO:0005730 nucleolus
Expand Tier II Mouse 1002 Genes GS84253: alcohol preference locus (Published QTL, Chr 11)
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 872 Genes GS186633: GO:0044093 positive regulation of molecular function
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Mouse GO 41 Genes GS184748: GO:0032200 telomere organization
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier III Mouse 1654 Genes GS37188: Positional candidate on Chromosome 11 (30-110 Mb) for dominant deviation measuring EtOH consumption during DID, 24 hour access and BEC.
Expand Tier I Mouse 870 Genes GS136651: skeletal size (tail length) 5 (Skl5, Published QTL Chr 11)
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 437 Genes GS208019: GO:0051347 positive regulation of transferase activity
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Mouse 990 Genes GS136439: peak bone density 1 (Pbd1, Published QTL Chr 11)
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 Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Mouse 768 Genes GS136398: organ weight 7 (Org7, Published QTL Chr 11)
Expand Tier I Human 77 Genes GS175692: HP:0200042 Skin ulcer
Expand Tier I Human 129 Genes GS173090: HP:0004377 Hematological neoplasm
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 33 Genes GS173533: HP:0001876 Pancytopenia
Expand Tier I Mouse 996 Genes GS135295: acute lung injury QTL 1 (Aliq1, Published QTL Chr 11)
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
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 Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Mouse 861 Genes GS136741: spermatocyte heat stress resistance 2 (Sphsr2, Published QTL Chr 11)
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 1126 Genes GS195108: GO:0071844 cellular component assembly at cellular level
Expand Tier I Mouse GO 690 Genes GS180673: GO:0044451 nucleoplasm part
Expand Tier I Human GO 4446 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 11 Genes GS203379: GO:0051972 regulation of telomerase activity
Expand Tier II Mouse 1017 Genes GS84254: nicotine sensitivity (Published QTL,Chr 11)
Expand Tier I Mouse 1004 Genes GS136517: platelet count 2 (Pltct2, Published QTL Chr 11)
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 553 Genes GS207972: GO:0030529 ribonucleoprotein complex
Expand Tier I Mouse 861 Genes GS136753: susceptibility to Salmonella typhimurium antigens 4 (Ssta4, Published QTL Chr 11)
Expand Tier I Human 155 Genes GS172040: HP:0000962 Hyperkeratosis
Expand Tier I Mouse 715 Genes GS128585: Rotarod Baseline Chr# 11
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 II Mouse 746 Genes GS84251: chronic alcohol withdrawal severity (Published QTL, Chr 11)
Expand Tier I Human 228 Genes GS172470: HP:0001743 Abnormality of the spleen
Expand Tier I Mouse GO 4518 Genes GS187751: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 869 Genes GS196719: GO:0006259 DNA metabolic process
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 Mouse GO 330 Genes GS191113: GO:0051347 positive regulation of transferase activity
Expand Tier I Mouse 848 Genes GS135349: Alzheimer's disease modifier 1 (Azdm1, Published QTL Chr 11)
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
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 Mouse GO 1662 Genes GS180155: GO:0065009 regulation of molecular function
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse 996 Genes GS135461: bone mineral density 7 (Bomd7, Published QTL Chr 11)
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 Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse 763 Genes GS135765: experimental allergic encephalomyelitis susceptibility 6b (Eae6b, Published QTL Chr 11)
Expand Tier I Human 198 Genes GS174236: HP:0000534 Abnormality of the eyebrow
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 Mouse GO 3 Genes GS192849: GO:0032203 telomere formation via telomerase
Expand Tier I Human 86 Genes GS175086: HP:0008388 Abnormality of the toenails
Expand Tier I Mouse 811 Genes GS136508: prion incubation determinant 3 (Pid3, Published QTL Chr 11)
Expand Tier I Mouse 850 Genes GS135939: HDL level 39 (Hdl39, Published QTL Chr 11)
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 Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Human 121 Genes GS173538: HP:0001873 Thrombocytopenia
Expand Tier I Human CTD 1522 Genes GS124579: Selenium interacting genes (MeSH:D012643) in CTD
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse 870 Genes GS135399: body growth early QTL 9 (Bgeq9, Published QTL Chr 11)
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 1334 Genes GS178975: GO:0022607 cellular component assembly
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Mouse GO 2595 Genes GS177357: GO:0003676 nucleic acid binding
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 Mouse GO 6 Genes GS185939: GO:0005697 telomerase holoenzyme complex
Expand Tier I Mouse GO 926 Genes GS178355: GO:0071844 cellular component assembly at cellular level
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