Gene Details



SMAD4 and homologs in 6 species are found in 1620 GeneSets:


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

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Mouse GO 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse MP 440 Genes GS170247: MP:0002038 carcinoma
Expand Tier I Human GO 20 Genes GS197033: GO:0030511 positive regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Mouse GO 894 Genes GS182704: GO:0051172 negative regulation of nitrogen compound metabolic process
Expand Tier I Human GO 195 Genes GS206380: GO:0001763 morphogenesis of a branching structure
Expand Tier I Mouse GO 1392 Genes GS184458: GO:0009892 negative regulation of metabolic process
Expand Tier I Mouse MP 201 Genes GS169431: MP:0010426 abnormal heart and great artery attachment
Expand Tier I Mouse GO 763 Genes GS191625: GO:0040007 growth
Expand Tier I Human GO 871 Genes GS198861: GO:0007167 enzyme linked receptor protein signaling pathway
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 158 Genes GS188071: GO:0042176 regulation of protein catabolic process
Expand Human 1393 Genes GS219979: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Mouse MP 596 Genes GS164506: MP:0001698 decreased embryo size
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse MP 3520 Genes GS169830: MP:0005384 cellular phenotype
Expand Tier I Mouse 267 Genes GS135266: age-related hearing loss 6 (Ahl6, Published QTL Chr 18)
Expand Tier I Mouse MP 255 Genes GS166949: MP:0009308 adenocarcinoma
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 110 Genes GS171784: HP:0001399 Hepatic failure
Expand Tier I Human GO 88 Genes GS199902: GO:0090316 positive regulation of intracellular protein transport
Expand Tier I Mouse MP 426 Genes GS165308: MP:0004848 abnormal liver size
Expand Human 2063 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 197 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human GO 598 Genes GS201231: GO:0060548 negative regulation of cell death
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Mouse MP 334 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Mouse MP 75 Genes GS168818: MP:0005431 decreased oocyte number
Expand Tier I Human CTD 111 Genes GS122521: Nitric Oxide interacting genes (MeSH:D009569) in CTD
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Mouse GO 3776 Genes GS187887: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 56 Genes GS203397: GO:0007492 endoderm development
Expand Tier I Human CTD 85 Genes GS125731: nitrofen interacting genes (MeSH:C007350) in CTD
Expand Tier I Mouse GO 179 Genes GS181529: GO:0010720 positive regulation of cell development
Expand Human 2063 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Mouse MP 124 Genes GS163468: MP:0010499 abnormal ventricle myocardium morphology
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier III Rat 422 Genes GS223382: Bone mineral density QTL 65 (Bmd65 Published QTL Chr 18)
Expand Tier I Mouse MP 2220 Genes GS166858: MP:0000685 abnormal immune system morphology
Expand Tier I Mouse 165 Genes GS129162: proteoglycan induced spondylitis 1 (Pgis1 Published QTL Chr 18)
Expand Tier I Mouse MP 430 Genes GS165850: MP:0000352 decreased cell proliferation
Expand Tier I Mouse MP 1002 Genes GS166749: MP:0002221 abnormal lymph organ size
Expand Tier I Mouse GO 3 Genes GS190853: GO:0032444 activin responsive factor complex
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Mouse GO 231 Genes GS192769: GO:0034504 protein localization to nucleus
Expand Tier I Human CTD 2014 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human GO 2878 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human GO 156 Genes GS207473: GO:0033157 regulation of intracellular protein transport
Expand Tier I Mouse GO 1833 Genes GS184324: GO:0010646 regulation of cell communication
Expand Tier I Mouse GO 779 Genes GS178588: GO:0045892 negative regulation of transcription, DNA-dependent
Expand Tier I Mouse GO 8 Genes GS188665: GO:0032525 somite rostral/caudal axis specification
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse MP 54 Genes GS167238: MP:0009153 increased pancreas tumor incidence
Expand Tier I Human 37 Genes GS176711: HP:0100585 Teleangiectasia of the skin
Expand Tier I Mouse GO 358 Genes GS181414: GO:0032880 regulation of protein localization
Expand Tier I Mouse GO 3080 Genes GS177265: GO:0048731 system development
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human 282 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Mouse GO 2955 Genes GS181893: GO:0048522 positive regulation of cellular process
Expand Tier I Mouse MP 93 Genes GS165080: MP:0001883 mammary adenocarcinoma
Expand Tier I Mouse MP 25 Genes GS168060: MP:0000298 absent atrioventricular cushions
Expand Tier I Mouse MP 902 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Mouse GO 64 Genes GS187973: GO:0061053 somite development
Expand Human 1733 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Mouse GO 4001 Genes GS183543: GO:0051179 localization
Expand Tier I Mouse GO 2762 Genes GS178357: GO:0071842 cellular component organization at cellular level
Expand Tier I Mouse MP 1019 Genes GS162953: MP:0002020 increased tumor incidence
Expand Tier I Mouse MP 123 Genes GS164422: MP:0010287 increased reproductive system tumor incidence
Expand Tier I Mouse MP 316 Genes GS169191: MP:0000281 abnormal interventricular septum morphology
Expand Tier I Mouse MP 440 Genes GS169082: MP:0002073 abnormal hair growth
Expand Tier I Human GO 200 Genes GS202527: GO:0032386 regulation of intracellular transport
Expand Tier I Mouse GO 4114 Genes GS193414: GO:0044249 cellular biosynthetic process
Expand Tier I Human CTD 577 Genes GS123943: Curcumin interacting genes (MeSH:D003474) in CTD
Expand Tier I Mouse GO 361 Genes GS187220: GO:0033365 protein localization to organelle
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Mouse MP 39 Genes GS162971: MP:0008011 intestine polyps
Expand Tier I Mouse MP 519 Genes GS165595: MP:0010545 abnormal heart layer morphology
Expand Tier I Mouse GO 912 Genes GS179236: GO:0048699 generation of neurons
Expand Tier I Mouse MP 368 Genes GS163926: MP:0004097 abnormal cerebellar cortex morphology
Expand Tier I Human 346 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Mouse GO 39 Genes GS180270: GO:0009948 anterior/posterior axis specification
Expand Tier I Human GO 1619 Genes GS204106: GO:0060089 molecular transducer activity
Expand Tier I Human 14 Genes GS172765: HP:0001680 Coarctation of aorta
Expand Tier I Mouse GO 472 Genes GS184456: GO:0009894 regulation of catabolic process
Expand Human 1393 Genes GS219985: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 40 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human 114 Genes GS170850: HP:0006265 Aplasia/Hypoplasia of fingers
Expand Tier I Mouse GO 758 Genes GS188757: GO:0009887 organ morphogenesis
Expand Tier I Human GO 1001 Genes GS198240: GO:0031399 regulation of protein modification process
Expand Tier I Mouse MP 59 Genes GS167039: MP:0003886 abnormal embryonic epiblast morphology
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 144 Genes GS179767: GO:0000976 transcription regulatory region sequence-specific DNA binding
Expand Tier I Mouse MP 96 Genes GS170556: MP:0000878 abnormal Purkinje cell number
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse MP 550 Genes GS164042: MP:0002018 malignant tumors
Expand Tier I Human GO 267 Genes GS204628: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human GO 1197 Genes GS201696: GO:0010941 regulation of cell death
Expand Tier I Human GO 3863 Genes GS201367: GO:0019538 protein metabolic process
Expand Human 1003 Genes GS221018: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human 101 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human 24 Genes GS172240: HP:0004936 Venous thrombosis
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 999 Genes GS195340: GO:0045893 positive regulation of transcription, DNA-dependent
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 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Mouse GO 3021 Genes GS182703: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Mouse MP 268 Genes GS164668: MP:0010293 increased integument system tumor incidence
Expand Tier III Rat 267 Genes GS223020: Body weight QTL 58 (Bw58 Published QTL Chr 18)
Expand Human 1470 Genes GS219947: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Mouse GO 4500 Genes GS186790: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse GO 352 Genes GS191375: GO:0005813 centrosome
Expand Tier I Mouse MP 974 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Mouse GO 88 Genes GS183102: GO:0090316 positive regulation of intracellular protein transport
Expand Tier I Human GO 1 Genes GS202009: GO:0030616 transforming growth factor beta receptor, common-partner cytoplasmic mediator activity
Expand Tier I Mouse 421 Genes GS136615: colon tumor susceptibility 5 (Scc5, Published QTL Chr 18)
Expand Tier I Mouse GO 331 Genes GS185545: GO:0044212 transcription regulatory region DNA binding
Expand Tier I Mouse GO 560 Genes GS186301: GO:0031401 positive regulation of protein modification process
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier III Rat 387 Genes GS224517: Body weight QTL 110 (Bw110 Published QTL Chr 18)
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 939 Genes GS168336: MP:0000367 abnormal coat/ hair morphology
Expand Tier I Mouse MP 1338 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Human GO 325 Genes GS202371: GO:0044212 transcription regulatory region DNA binding
Expand Tier I Human 10 Genes GS174848: HP:0200008 Intestinal polyposis
Expand Tier I Human GO 2734 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Mouse GO 197 Genes GS189510: GO:0001763 morphogenesis of a branching structure
Expand Tier I Human 146 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human GO 1853 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier III Rat 187 Genes GS224279: Serum aldosterone level QTL 2 (Sald2 Published QTL Chr 18)
Expand Tier I Human GO 535 Genes GS194735: GO:0030163 protein catabolic process
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Mouse GO 123 Genes GS184009: GO:0048762 mesenchymal cell differentiation
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Mouse GO 5892 Genes GS180036: GO:0032501 multicellular organismal process
Expand Tier I Mouse GO 825 Genes GS187237: GO:0030182 neuron differentiation
Expand Tier I Human GO 1245 Genes GS195710: GO:0032268 regulation of cellular protein metabolic process
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3383 Genes GS200312: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Human GO 67 Genes GS204256: GO:0030510 regulation of BMP signaling pathway
Expand Tier I Mouse MP 217 Genes GS165355: MP:0003229 abnormal vitelline vasculature morphology
Expand Tier I Mouse GO 713 Genes GS177859: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 633 Genes GS195594: GO:0010562 positive regulation of phosphorus metabolic process
Expand Tier I Human GO 255 Genes GS194492: GO:0001942 hair follicle development
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 60 Genes GS173119: HP:0002315 Headache
Expand Tier I Human GO 168 Genes GS195660: GO:0061138 morphogenesis of a branching epithelium
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse MP 1056 Genes GS169389: MP:0002060 abnormal skin morphology
Expand Tier I Mouse MP 1430 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse MP 2432 Genes GS167542: MP:0001790 abnormal immune system physiology
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Mouse MP 97 Genes GS164579: MP:0010500 myocardium hypoplasia
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 1001 Genes GS201264: GO:0009890 negative regulation of biosynthetic process
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Mouse MP 125 Genes GS163083: MP:0010279 increased gastrointestinal tumor incidence
Expand Human 156 Genes GS219668: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Human GO 525 Genes GS208562: GO:0040008 regulation of growth
Expand Tier I Human 54 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Human 32 Genes GS175790: HP:0008771 Aplasia/Hypoplasia of the ear
Expand Tier I Human GO 277 Genes GS193992: GO:0048732 gland development
Expand Tier I Human GO 174 Genes GS198821: GO:0051098 regulation of binding
Expand Tier I Mouse MP 47 Genes GS164397: MP:0008000 increased ovary tumor incidence
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 1428 Genes GS201262: GO:0009892 negative regulation of metabolic process
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Mouse GO 994 Genes GS178589: GO:0045893 positive regulation of transcription, DNA-dependent
Expand Tier I Mouse GO 933 Genes GS178813: GO:0046983 protein dimerization activity
Expand Tier I Human GO 494 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human 66 Genes GS174437: HP:0005114 Abnormalities of the peripheral arteries
Expand Tier I Human 93 Genes GS170972: HP:0001933 Subcutaneous hemorrhage
Expand Human 80 Genes GS220968: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PROGESTERONE_MEDIATED_OOCYTE_MATURATION
Expand Tier I Mouse GO 444 Genes GS177990: GO:0030163 protein catabolic process
Expand Tier I Mouse GO 13 Genes GS177538: GO:0072074 kidney mesenchyme development
Expand Tier I Human GO 1000 Genes GS199986: GO:0009719 response to endogenous stimulus
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier III Rat 397 Genes GS223848: Serum corticosterone level QTL 22 (Scort22 Published QTL Chr 18)
Expand Tier I Human 93 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human CTD 4 Genes GS126077: FR 167653 interacting genes (MeSH:C104334) in CTD
Expand Tier I Human GO 676 Genes GS196540: GO:0043565 sequence-specific DNA binding
Expand Tier I Human 6 Genes GS175970: HP:0100784 Peripheral arteriovenous fistula
Expand Tier I Mouse GO 839 Genes GS181450: GO:0031399 regulation of protein modification process
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 Human 189 Genes GS220974: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CHEMOKINE_SIGNALING_PATHWAY
Expand Tier I Mouse DRG 2567 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 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Mouse GO 4218 Genes GS192073: GO:1901576 organic substance biosynthetic process
Expand Tier I Mouse MP 9 Genes GS167256: MP:0009374 absent cumulus expansion
Expand Tier I Mouse MP 86 Genes GS169684: MP:0010783 abnormal stomach wall morphology
Expand Tier I Human GO 1179 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Tier I Mouse GO 125 Genes GS178016: GO:0042633 hair cycle
Expand Tier I Human 208 Genes GS175164: HP:0011927 Short digit
Expand Tier I Mouse GO 369 Genes GS181032: GO:0001701 in utero embryonic development
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Mouse MP 47 Genes GS165335: MP:0010308 decreased tumor latency
Expand Tier I Mouse GO 3293 Genes GS186214: GO:0048518 positive regulation of biological process
Expand Tier I Mouse MP 348 Genes GS168152: MP:0005501 abnormal skin physiology
Expand Human 1003 Genes GS219719: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Human 156 Genes GS220986: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Mouse GO 827 Genes GS180025: GO:0046907 intracellular transport
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 121 Genes GS163262: MP:0003763 abnormal thymus physiology
Expand Tier I Human GO 2 Genes GS194272: GO:0072076 nephrogenic mesenchyme development
Expand Tier I Human GO 247 Genes GS200142: GO:0001666 response to hypoxia
Expand Tier I Mouse MP 48 Genes GS170193: MP:0002928 abnormal bile duct morphology
Expand Tier I Human GO 1692 Genes GS203755: GO:0016265 death
Expand Tier I Mouse MP 2551 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Mouse MP 1548 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Mouse 221 Genes GS135757: experimental allergic encephalomyelitis susceptibility 25 (Eae25, Published QTL Chr 18)
Expand Tier III Rat 267 Genes GS223664: Body weight QTL 103 (Bw103 Published QTL Chr 18)
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 21 Genes GS209576: GO:0072132 mesenchyme morphogenesis
Expand Tier I Mouse GO 5247 Genes GS178448: GO:0005634 nucleus
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 276 Genes GS206934: GO:0051223 regulation of protein transport
Expand Tier I Human 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human CTD 85 Genes GS125044: Acetaldehyde interacting genes (MeSH:D000079) in CTD
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human GO 1123 Genes GS196794: GO:0046907 intracellular transport
Expand Human 1197 Genes GS219976: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Mouse MP 2112 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse 201 Genes GS135963: HDL QTL 31 (Hdlq31, Published QTL Chr 18)
Expand Tier I Mouse GO 577 Genes GS182069: GO:0007167 enzyme linked receptor protein signaling pathway
Expand Tier I Human GO 376 Genes GS208298: GO:0005813 centrosome
Expand Tier I Human GO 811 Genes GS195339: GO:0045892 negative regulation of transcription, DNA-dependent
Expand Tier I Human GO 890 Genes GS203289: GO:0071822 protein complex subunit organization
Expand Tier I Mouse GO 1575 Genes GS188290: GO:0009966 regulation of signal transduction
Expand Tier I Human 36 Genes GS172711: HP:0000219 Thin upper lip vermilion
Expand Tier I Human 49 Genes GS173059: HP:0000322 Short philtrum
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 187 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Mouse MP 367 Genes GS166150: MP:0001577 anemia
Expand Tier I Mouse MP 32 Genes GS163946: MP:0011106 partial embryonic lethality between implantation and somite formation
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse GO 926 Genes GS192344: GO:0010629 negative regulation of gene expression
Expand Tier III Rat 96 Genes GS223441: Blood pressure QTL 234 (Bp234 Published QTL Chr 18)
Expand Tier I Mouse MP 2204 Genes GS165615: MP:0002123 abnormal hematopoiesis
Expand Human 156 Genes GS222102: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier III Rat 656 Genes GS223687: Blood pressure QTL 232 (Bp232 Published QTL Chr 18)
Expand Tier I Human GO 2321 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Mouse MP 270 Genes GS170555: MP:0000875 abnormal cerebellar Purkinje cell layer
Expand Tier I Mouse GO 5879 Genes GS187160: GO:0044707 single-multicellular organism process
Expand Tier I Human 41 Genes GS171157: HP:0100742 Vascular neoplasm
Expand Tier I Mouse GO 2981 Genes GS177761: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Mouse GO 66 Genes GS191776: GO:0001837 epithelial to mesenchymal transition
Expand Tier I Mouse GO 1684 Genes GS181783: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 195 Genes GS198647: GO:0045926 negative regulation of growth
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 2939 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human GO 154 Genes GS198319: GO:0010720 positive regulation of cell development
Expand Tier I Mouse MP 3168 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier I Human 187 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Mouse MP 72 Genes GS168994: MP:0005083 abnormal biliary tract morphology
Expand Tier I Human GO 4 Genes GS209577: GO:0072131 kidney mesenchyme morphogenesis
Expand Tier I Human 28 Genes GS172285: HP:0000826 Precocious puberty
Expand Tier I Mouse MP 688 Genes GS163620: MP:0002086 abnormal extraembryonic tissue morphology
Expand Tier I Mouse MP 186 Genes GS167553: MP:0003448 altered tumor morphology
Expand Tier I Mouse GO 1081 Genes GS180977: GO:0045184 establishment of protein localization
Expand Tier I Mouse MP 107 Genes GS164968: MP:0001726 abnormal allantois morphology
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse GO 524 Genes GS190178: GO:0051050 positive regulation of transport
Expand Tier I Mouse MP 1669 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human GO 697 Genes GS210236: GO:0000904 cell morphogenesis involved in differentiation
Expand Tier I Mouse MP 415 Genes GS164482: MP:0001216 abnormal epidermal layer morphology
Expand Tier I Mouse MP 60 Genes GS164286: MP:0002574 increased vertical activity
Expand Tier I Mouse GO 203 Genes GS188441: GO:0045165 cell fate commitment
Expand Tier I Human 14 Genes GS171923: HP:0100579 Mucosal telangiectasiae
Expand Tier I Mouse MP 14 Genes GS166491: MP:0005186 increased circulating progesterone level
Expand Human 1393 Genes GS219948: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Mouse GO 93 Genes GS185690: GO:0032388 positive regulation of intracellular transport
Expand Tier I Human GO 890 Genes GS207863: GO:0009057 macromolecule catabolic process
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Mouse MP 510 Genes GS164555: MP:0005329 abnormal myocardium layer morphology
Expand Tier I Human 15 Genes GS171345: HP:0001048 Cavernous hemangioma
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Mouse GO 271 Genes GS189322: GO:0048589 developmental growth
Expand Tier I Mouse MP 25 Genes GS170304: MP:0003414 epidermal cyst
Expand Tier I Mouse MP 311 Genes GS166634: MP:0001126 abnormal ovary morphology
Expand Tier I Human GO 4 Genes GS194705: GO:0071141 SMAD protein complex
Expand Tier I Human GO 18 Genes GS208565: GO:0070412 R-SMAD binding
Expand Tier I Human GO 11 Genes GS206223: GO:0060390 regulation of SMAD protein import into nucleus
Expand Tier I Mouse GO 2279 Genes GS186488: GO:0048513 organ development
Expand Tier I Human GO 1619 Genes GS202760: GO:0004871 signal transducer activity
Expand Tier I Mouse GO 479 Genes GS188558: GO:0042327 positive regulation of phosphorylation
Expand Tier I Mouse MP 3396 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human GO 26 Genes GS200410: GO:0010862 positive regulation of pathway-restricted SMAD protein phosphorylation
Expand Tier I Human GO 798 Genes GS206428: GO:0001932 regulation of protein phosphorylation
Expand Tier I Human 483 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human GO 459 Genes GS197665: GO:0051248 negative regulation of protein metabolic process
Expand Tier I Mouse MP 3159 Genes GS169095: MP:0004924 abnormal behavior
Expand Human 129 Genes GS222839: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_NEUROTRANSMITTER_RECEPTOR_BINDING_AND_DOWNSTREAM_TRANSMISSION_IN_THE_POSTSYNAPTIC_CELL
Expand Tier I Human GO 551 Genes GS206430: GO:0001934 positive regulation of protein phosphorylation
Expand Tier I Mouse MP 68 Genes GS167556: MP:0009364 abnormal mature ovarian follicle morphology
Expand Tier I Mouse GO 777 Genes GS178522: GO:0070727 cellular macromolecule localization
Expand Tier I Mouse MP 1925 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human GO 1820 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Mouse MP 343 Genes GS166160: MP:0011092 complete embryonic lethality
Expand Tier I Human GO 29 Genes GS197821: GO:0001702 gastrulation with mouth forming second
Expand Tier I Mouse MP 8 Genes GS162857: MP:0010690 thick hair follicle outer rooth sheath
Expand Tier I Mouse GO 8 Genes GS177267: GO:0048733 sebaceous gland development
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 315 Genes GS204842: GO:0003682 chromatin binding
Expand Tier I Human GO 1430 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Mouse MP 59 Genes GS167995: MP:0002404 increased intestinal adenoma incidence
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Mouse GO 1398 Genes GS181215: GO:0007399 nervous system development
Expand Tier I Mouse GO 62 Genes GS187394: GO:0030510 regulation of BMP signaling pathway
Expand Tier I Human 278 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Mouse MP 189 Genes GS164182: MP:0000489 abnormal large intestine morphology
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1212 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier III Rat 267 Genes GS223655: Body weight QTL 107 (Bw107 Published QTL Chr 18)
Expand Tier I Mouse MP 442 Genes GS165816: MP:0001119 abnormal female reproductive system morphology
Expand Tier I Mouse GO 1172 Genes GS179822: GO:0006468 protein phosphorylation
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Human 1003 Genes GS221267: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Mouse GO 1176 Genes GS182705: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1745 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Mouse MP 46 Genes GS164244: MP:0001685 abnormal endoderm development
Expand Tier I Human GO 36 Genes GS199081: GO:0045682 regulation of epidermis development
Expand Tier I Mouse GO 2876 Genes GS181102: GO:0043228 non-membrane-bounded organelle
Expand Human 1197 Genes GS219982: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Mouse GO 57 Genes GS190025: GO:0001658 branching involved in ureteric bud morphogenesis
Expand Tier I Human 123 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Mouse GO 15 Genes GS178021: GO:0042634 regulation of hair cycle
Expand Tier I Mouse GO 1298 Genes GS183756: GO:0010605 negative regulation of macromolecule metabolic process
Expand Tier I Mouse GO 284 Genes GS182194: GO:0005667 transcription factor complex
Expand Tier I Human GO 480 Genes GS207071: GO:0051050 positive regulation of transport
Expand Tier I Human GO 239 Genes GS209714: GO:0034504 protein localization to nucleus
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Mouse GO 241 Genes GS185901: GO:0017038 protein import
Expand Tier I Mouse MP 794 Genes GS169062: MP:0000913 abnormal brain development
Expand Tier I Mouse 456 Genes GS136197: lung squamous cell carcinoma 3 (Lscc3, Published QTL Chr 18)
Expand Tier I Mouse GO 23359 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Mouse GO 466 Genes GS191722: GO:0008285 negative regulation of cell proliferation
Expand Tier I Mouse MP 1065 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Mouse MP 148 Genes GS166180: MP:0010299 increased mammary gland tumor incidence
Expand Tier I Mouse GO 868 Genes GS180149: GO:0065003 macromolecular complex assembly
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 2455 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human GO 17 Genes GS206220: GO:0060395 SMAD protein signal transduction
Expand Tier III Mouse 476 Genes GS791: CerebellarFissureFreq BXD Cerebellum Gene Expression Correlates of Fissure Frequency
Expand Tier I Mouse GO 1860 Genes GS177717: GO:0051239 regulation of multicellular organismal process
Expand Tier I Mouse GO 4588 Genes GS177309: GO:1901363 heterocyclic compound binding
Expand Tier I Mouse GO 180 Genes GS182030: GO:0051098 regulation of binding
Expand Tier I Mouse GO 18 Genes GS189356: GO:0060395 SMAD protein signal transduction
Expand Tier I Mouse MP 112 Genes GS169200: MP:0006361 abnormal female germ cell morphology
Expand Human 1197 Genes GS219725: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE_PART
Expand Tier I Mouse GO 23 Genes GS192636: GO:0072132 mesenchyme morphogenesis
Expand Tier I Mouse GO 2595 Genes GS188410: GO:0032774 RNA biosynthetic process
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Mouse GO 1322 Genes GS191727: GO:0008283 cell proliferation
Expand Tier I Mouse MP 482 Genes GS167105: MP:0008948 decreased neuron number
Expand Tier I Human GO 59 Genes GS205619: GO:0009880 embryonic pattern specification
Expand Tier I Mouse MP 50 Genes GS166270: MP:0009583 increased keratinocyte proliferation
Expand Tier I Human GO 498 Genes GS202005: GO:0006605 protein targeting
Expand Tier I Mouse MP 161 Genes GS164663: MP:0010298 increased respiratory system tumor incidence
Expand Tier I Human GO 81 Genes GS201261: GO:0009895 negative regulation of catabolic process
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 290 Genes GS198991: GO:0005667 transcription factor complex
Expand Tier I Human GO 157 Genes GS201548: GO:0048754 branching morphogenesis of a tube
Expand Tier I Mouse DRG 1196 Genes provisional GS87137: Table S2: List of probe-sets of genes differentially expressed among the four inbred strains of mice. Gene Ranks [DRG]
Expand Tier I Mouse 99 Genes GS129141: insulin dependent diabetes susceptibility 21.2 (Idd21.2 Published QTL Chr 18)
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 70 Genes GS206319: GO:0034764 positive regulation of transmembrane transport
Expand Tier I Human 10 Genes GS174952: HP:0100761 Visceral angiomatosis
Expand Tier I Mouse GO 196 Genes GS185696: GO:0032386 regulation of intracellular transport
Expand Tier I Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier I Mouse GO 4637 Genes GS177382: GO:0097159 organic cyclic compound binding
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 16 Genes GS175069: HP:0001409 Portal hypertension
Expand Tier I Mouse GO 279 Genes GS177818: GO:0043623 cellular protein complex assembly
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Mouse MP 45 Genes GS163043: MP:0003085 abnormal egg cylinder morphology
Expand Tier I Human 6 Genes GS172985: HP:0004947 Arteriovenous fistula
Expand Tier I Human 390 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier III Rat 350 Genes GS223997: Glucose level QTL 55 (Gluco55 Published QTL Chr 18)
Expand Tier I Mouse GO 32 Genes GS181031: GO:0001702 gastrulation with mouth forming second
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 1682 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Mouse GO 580 Genes GS177903: GO:0042803 protein homodimerization activity
Expand Tier I Mouse MP 837 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Mouse MP 1731 Genes GS168956: MP:0003491 abnormal voluntary movement
Expand Tier I Human 128 Genes GS171905: HP:0004297 Abnormality of the biliary system
Expand Tier I Mouse MP 87 Genes GS168889: MP:0000297 abnormal atrioventricular cushion morphology
Expand Tier I Mouse GO 549 Genes GS183491: GO:0060284 regulation of cell development
Expand Tier I Human 138 Genes GS174289: HP:0002577 Abnormality of the stomach
Expand Tier I Human 134 Genes GS171627: HP:0000470 Short neck
Expand Tier III Rat 217 Genes GS223280: Blood pressure QTL 354 (Bp354 Published QTL Chr 18)
Expand Tier I Mouse GO 146 Genes GS190148: GO:0060485 mesenchyme development
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Mouse GO 1075 Genes GS185961: GO:0051049 regulation of transport
Expand Tier I Human GO 1228 Genes GS199113: GO:0015031 protein transport
Expand Tier I Mouse GO 1715 Genes GS193237: GO:0031325 positive regulation of cellular metabolic process
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Mouse GO 31 Genes GS189361: GO:0060393 regulation of pathway-restricted SMAD protein phosphorylation
Expand Tier I Mouse MP 3424 Genes GS163934: MP:0001764 abnormal homeostasis
Expand Tier I Mouse GO 4333 Genes GS184452: GO:0044422 organelle part
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse MP 4902 Genes GS165525: MP:0010768 mortality/aging
Expand Tier I Mouse GO 1608 Genes GS193639: GO:0051641 cellular localization
Expand Tier I Mouse MP 747 Genes GS170442: MP:0010866 abnormal prenatal body size
Expand Tier I Human GO 688 Genes GS194602: GO:0045944 positive regulation of transcription from RNA polymerase II promoter
Expand Tier I Mouse MP 243 Genes GS170553: MP:0000877 abnormal Purkinje cell morphology
Expand Human 1470 Genes GS219730: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Mouse GO 129 Genes GS184206: GO:0036293 response to decreased oxygen levels
Expand Tier I Human GO 1157 Genes GS206657: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Mouse GO 280 Genes GS190050: GO:0051223 regulation of protein transport
Expand Tier I Human 2 Genes GS172708: HP:0003720 Generalized muscle hypertrophy
Expand Tier I Human GO 265 Genes GS197236: GO:0070482 response to oxygen levels
Expand Tier I Human GO 1925 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 3 Genes GS175873: HP:0006574 Hepatic arteriovenous malformation
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse GO 427 Genes GS190314: GO:0035295 tube development
Expand Tier I Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Mouse DRG 2567 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 Mouse MP 84 Genes GS169668: MP:0002014 increased papilloma incidence
Expand Tier I Human 39 Genes GS173054: HP:0000327 Hypoplasia of the maxilla
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Mouse GO 346 Genes GS189454: GO:0034762 regulation of transmembrane transport
Expand Tier I Mouse GO 1078 Genes GS193009: GO:0042127 regulation of cell proliferation
Expand Tier I Mouse MP 222 Genes GS168827: MP:0010402 ventricular septal defect
Expand Tier I Mouse MP 195 Genes GS170701: MP:0004847 abnormal liver weight
Expand Tier I Human 18 Genes GS173220: HP:0006707 Abnormality of the hepatic vasculature
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human GO 86 Genes GS204040: GO:0009798 axis specification
Expand Tier I Mouse GO 2917 Genes GS190067: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human GO 708 Genes GS203147: GO:0031401 positive regulation of protein modification process
Expand Tier I Mouse 208 Genes GS135922: growth traits 7 (Gwth7, Published QTL Chr 18)
Expand Tier I Mouse MP 251 Genes GS169609: MP:0001674 abnormal triploblastic development
Expand Tier I Mouse MP 126 Genes GS168434: MP:0002981 increased liver weight
Expand Tier I Human 267 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 3 Genes GS175820: HP:0002408 Cerebral arteriovenous malformation
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human CTD 1399 Genes GS124312: sodium arsenite interacting genes (MeSH:C017947) in CTD
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 841 Genes GS202079: GO:0051253 negative regulation of RNA metabolic process
Expand Tier I Mouse GO 291 Genes GS186966: GO:0051169 nuclear transport
Expand Tier I Human GO 18 Genes GS203186: GO:0071634 regulation of transforming growth factor beta production
Expand Tier I Human 1 Genes GS176398: HP:0004784 Juvenile gastrointestinal polyposis
Expand Tier I Mouse MP 563 Genes GS166535: MP:0010865 prenatal growth retardation
Expand Tier I Human GO 36 Genes GS194990: GO:0001159 core promoter proximal region DNA binding
Expand Tier I Human GO 167 Genes GS204627: GO:0007179 transforming growth factor beta receptor signaling pathway
Expand Tier I Human GO 4 Genes GS209575: GO:0072133 metanephric mesenchyme morphogenesis
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Mouse GO 55 Genes GS185983: GO:0001756 somitogenesis
Expand Tier I Mouse GO 36 Genes GS177723: GO:0010717 regulation of epithelial to mesenchymal transition
Expand Tier I Human GO 1690 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 1135 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human GO 486 Genes GS208302: GO:0005815 microtubule organizing center
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse GO 7552 Genes GS180452: GO:0044237 cellular metabolic process
Expand Tier I Mouse MP 35 Genes GS170516: MP:0010684 abnormal hair follicle outer root sheath morphology
Expand Tier I Human GO 339 Genes GS203827: GO:0051169 nuclear transport
Expand Tier I Human GO 70 Genes GS196572: GO:0060021 palate development
Expand Tier I Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human GO 966 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 4 Genes GS174288: HP:0002576 Intussusception
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier III Rat 200 Genes GS224065: Kidney mass QTL 2 (Kidm2 Published QTL Chr 18)
Expand Tier I Human GO 927 Genes GS208787: GO:0034613 cellular protein localization
Expand Tier I Mouse GO 1140 Genes GS188751: GO:0044430 cytoskeletal part
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process