Gene Details



SMAD4 and homologs in 4 species are found in 1520 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 7755 Genes GS185131: GO:0044699 single-organism process
Expand Tier I Mouse MP 453 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 220 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 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Mouse GO 158 Genes GS188071: GO:0042176 regulation of protein catabolic process
Expand Tier I Mouse MP 599 Genes GS164506: MP:0001698 decreased embryo size
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Mouse MP 3631 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 264 Genes GS166949: MP:0009308 adenocarcinoma
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 Human GO 88 Genes GS199902: GO:0090316 positive regulation of intracellular protein transport
Expand Tier I Mouse MP 469 Genes GS165308: MP:0004848 abnormal liver size
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human GO 600 Genes GS201231: GO:0060548 negative regulation of cell death
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Mouse MP 343 Genes GS166753: MP:0001935 decreased litter size
Expand Tier I Mouse MP 76 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 177 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 Tier I Mouse MP 124 Genes GS163468: MP:0010499 abnormal ventricle myocardium morphology
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Mouse MP 2406 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 436 Genes GS165850: MP:0000352 decreased cell proliferation
Expand Tier I Mouse MP 1084 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 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human GO 2896 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 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse MP 55 Genes GS167238: MP:0009153 increased pancreas tumor incidence
Expand Tier I Human 38 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 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human 283 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 94 Genes GS165080: MP:0001883 mammary adenocarcinoma
Expand Tier I Mouse MP 25 Genes GS168060: MP:0000298 absent atrioventricular cushions
Expand Tier I Mouse MP 1008 Genes GS164333: MP:0000516 abnormal renal/urinary system morphology
Expand Tier I Mouse GO 64 Genes GS187973: GO:0061053 somite development
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 1172 Genes GS162953: MP:0002020 increased tumor incidence
Expand Tier I Mouse MP 128 Genes GS164422: MP:0010287 increased reproductive system tumor incidence
Expand Tier I Mouse MP 336 Genes GS169191: MP:0000281 abnormal interventricular septum morphology
Expand Tier I Mouse MP 445 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 578 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 520 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 375 Genes GS163926: MP:0004097 abnormal cerebellar cortex morphology
Expand Tier I Human 348 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 1639 Genes GS204106: GO:0060089 molecular transducer activity
Expand Tier I Human 15 Genes GS172765: HP:0001680 Coarctation of aorta
Expand Tier I Mouse GO 472 Genes GS184456: GO:0009894 regulation of catabolic process
Expand Tier I Human 41 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human 115 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 1004 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 1393 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 99 Genes GS170556: MP:0000878 abnormal Purkinje cell number
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Mouse MP 570 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 1202 Genes GS201696: GO:0010941 regulation of cell death
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Mouse GO 2565 Genes GS192299: GO:0006793 phosphorus metabolic process
Expand Tier I Human 102 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human 25 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 186 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 303 Genes GS164668: MP:0010293 increased integument system tumor incidence
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 1041 Genes GS168683: MP:0000598 abnormal liver morphology
Expand Tier I Human GO 5452 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 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Mouse GO 8386 Genes GS189751: GO:0050794 regulation of cellular process
Expand Tier I Mouse MP 956 Genes GS168336: MP:0000367 abnormal coat/ hair morphology
Expand Tier I Mouse MP 1420 Genes GS163052: MP:0000266 abnormal heart morphology
Expand Tier I Human GO 328 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 2741 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 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human GO 535 Genes GS194735: GO:0030163 protein catabolic process
Expand Tier I Human 1073 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 2121 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 1249 Genes GS195710: GO:0032268 regulation of cellular protein metabolic process
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 3401 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 636 Genes GS195594: GO:0010562 positive regulation of phosphorus metabolic process
Expand Tier I Human GO 257 Genes GS194492: GO:0001942 hair follicle development
Expand Tier I Human 784 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 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Mouse MP 1104 Genes GS169389: MP:0002060 abnormal skin morphology
Expand Tier I Mouse MP 1460 Genes GS164264: MP:0002082 postnatal lethality
Expand Tier I Mouse MP 2955 Genes GS167542: MP:0001790 abnormal immune system physiology
Expand Tier I Human GO 3104 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 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 1003 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 127 Genes GS163083: MP:0010279 increased gastrointestinal tumor incidence
Expand Tier I Human GO 526 Genes GS208562: GO:0040008 regulation of growth
Expand Tier I Human 56 Genes GS176099: HP:0000926 Platyspondyly
Expand Tier I Human 33 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 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 1430 Genes GS201262: GO:0009892 negative regulation of metabolic process
Expand Tier I Human 913 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 493 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 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 1001 Genes GS199986: GO:0009719 response to endogenous stimulus
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 94 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 680 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 14644 Genes GS208012: GO:0044464 cell part
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 5369 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 87 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 211 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 3409 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 352 Genes GS168152: MP:0005501 abnormal skin physiology
Expand Tier I Human GO 1439 Genes GS205623: GO:0009888 tissue development
Expand Tier I Mouse GO 827 Genes GS180025: GO:0046907 intracellular transport
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Mouse MP 124 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 248 Genes GS200142: GO:0001666 response to hypoxia
Expand Tier I Mouse MP 51 Genes GS170193: MP:0002928 abnormal bile duct morphology
Expand Tier I Human GO 1699 Genes GS203755: GO:0016265 death
Expand Tier I Mouse MP 2821 Genes GS169535: MP:0005397 hematopoietic system phenotype
Expand Tier I Mouse MP 1615 Genes GS165789: MP:0005369 muscle phenotype
Expand Tier I Mouse GO 863 Genes GS177902: GO:0042802 identical protein binding
Expand Tier I Human 553 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 I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 3861 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 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human GO 277 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 1127 Genes GS196794: GO:0046907 intracellular transport
Expand Tier I Mouse MP 2199 Genes GS165244: MP:0010771 integument phenotype
Expand Tier I Human GO 14623 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 813 Genes GS195339: GO:0045892 negative regulation of transcription, DNA-dependent
Expand Tier I Human GO 893 Genes GS203289: GO:0071822 protein complex subunit organization
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 1575 Genes GS188290: GO:0009966 regulation of signal transduction
Expand Tier I Mouse GO 2538 Genes GS190893: GO:0030154 cell differentiation
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Mouse MP 376 Genes GS166150: MP:0001577 anemia
Expand Tier I Mouse MP 33 Genes GS163946: MP:0011106 partial embryonic lethality between implantation and somite formation
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Mouse GO 926 Genes GS192344: GO:0010629 negative regulation of gene expression
Expand Tier I Mouse MP 2404 Genes GS165615: MP:0002123 abnormal hematopoiesis
Expand Tier I Human GO 2335 Genes GS206192: GO:0048583 regulation of response to stimulus
Expand Tier I Mouse MP 273 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 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human GO 3275 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 3307 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 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 2957 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human 1060 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 3815 Genes GS169827: MP:0005387 immune system phenotype
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Mouse MP 101 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 692 Genes GS163620: MP:0002086 abnormal extraembryonic tissue morphology
Expand Tier I Mouse MP 221 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 5962 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Mouse GO 6204 Genes GS184629: GO:0005515 protein binding
Expand Tier I Mouse MP 1692 Genes GS169603: MP:0001672 abnormal embryogenesis/ development
Expand Tier I Mouse MP 418 Genes GS164482: MP:0001216 abnormal epidermal layer morphology
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 Tier I Mouse GO 93 Genes GS185690: GO:0032388 positive regulation of intracellular transport
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Mouse MP 316 Genes GS166634: MP:0001126 abnormal ovary morphology
Expand Tier I Human GO 18 Genes GS208565: GO:0070412 R-SMAD binding
Expand Tier I Mouse MP 3494 Genes GS170601: MP:0005621 abnormal cell physiology
Expand Tier I Human GO 801 Genes GS206428: GO:0001932 regulation of protein phosphorylation
Expand Tier I Human 487 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 3543 Genes GS169095: MP:0004924 abnormal behavior
Expand Tier I Human GO 554 Genes GS206430: GO:0001934 positive regulation of protein phosphorylation
Expand Tier I Mouse GO 777 Genes GS178522: GO:0070727 cellular macromolecule localization
Expand Tier I Mouse MP 1963 Genes GS166718: MP:0002169 no abnormal phenotype detected
Expand Tier I Human GO 1825 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Mouse MP 349 Genes GS166160: MP:0011092 complete embryonic lethality
Expand Tier I Human GO 30 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 Human GO 315 Genes GS204842: GO:0003682 chromatin binding
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 530 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 1213 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Mouse MP 455 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 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
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 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 481 Genes GS207071: GO:0051050 positive regulation of transport
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 815 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 MP 1130 Genes GS163227: MP:0003313 abnormal locomotor activation
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Mouse GO 1860 Genes GS177717: GO:0051239 regulation of multicellular organismal process
Expand Tier I Mouse GO 23 Genes GS192636: GO:0072132 mesenchyme morphogenesis
Expand Tier I Mouse GO 2710 Genes GS192471: GO:0048869 cellular developmental process
Expand Tier I Mouse GO 1322 Genes GS191727: GO:0008283 cell proliferation
Expand Tier I Mouse MP 487 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 177 Genes GS164663: MP:0010298 increased respiratory system tumor incidence
Expand Tier I Mouse DRG 1187 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 Human GO 4446 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 Human 111 Genes GS177023: HP:0010876 Abnormality of circulating protein level
Expand Tier I Mouse GO 279 Genes GS177818: GO:0043623 cellular protein complex assembly
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Mouse MP 46 Genes GS163043: MP:0003085 abnormal egg cylinder morphology
Expand Tier I Human 6 Genes GS172985: HP:0004947 Arteriovenous fistula
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Mouse GO 580 Genes GS177903: GO:0042803 protein homodimerization activity
Expand Tier I Mouse MP 940 Genes GS165876: MP:0002135 abnormal kidney morphology
Expand Tier I Human 130 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 136 Genes GS171627: HP:0000470 Short neck
Expand Tier I Mouse GO 1075 Genes GS185961: GO:0051049 regulation of transport
Expand Tier I Human GO 1231 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 GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse MP 246 Genes GS170553: MP:0000877 abnormal Purkinje cell morphology
Expand Tier I Mouse GO 129 Genes GS184206: GO:0036293 response to decreased oxygen levels
Expand Tier I Human GO 1160 Genes GS206657: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Mouse GO 427 Genes GS190314: GO:0035295 tube development
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 Mouse GO 346 Genes GS189454: GO:0034762 regulation of transmembrane transport
Expand Tier I Mouse MP 229 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 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 711 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 Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human GO 3287 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human CTD 1398 Genes GS124312: sodium arsenite interacting genes (MeSH:C017947) in CTD
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Mouse GO 291 Genes GS186966: GO:0051169 nuclear transport
Expand Tier I Human 1 Genes GS176398: HP:0004784 Juvenile gastrointestinal polyposis
Expand Tier I Human GO 36 Genes GS194990: GO:0001159 core promoter proximal region DNA binding
Expand Tier I Human 358 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 1697 Genes GS194905: GO:0008219 cell death
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule 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 Mouse GO 2991 Genes GS182469: GO:0043234 protein complex
Expand Tier I Human GO 969 Genes GS195570: GO:0046983 protein dimerization activity
Expand Tier I Human GO 3640 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 4 Genes GS174288: HP:0002576 Intussusception
Expand Tier I Human GO 3446 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 3721 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human GO 143 Genes GS196530: GO:0000976 transcription regulatory region sequence-specific DNA binding
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
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 MP 31 Genes GS167674: MP:0003208 abnormal neuromere morphology
Expand Tier I Mouse GO 18 Genes GS190593: GO:0071604 transforming growth factor beta production
Expand Tier I Human GO 1324 Genes GS207293: GO:0032879 regulation of localization
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 257 Genes GS208672: GO:0022404 molting cycle process
Expand Tier I Mouse GO 1208 Genes GS177214: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Mouse GO 301 Genes GS182956: GO:0035239 tube morphogenesis
Expand Tier I Mouse GO 2350 Genes GS185921: GO:0004871 signal transducer activity
Expand Tier I Mouse MP 41 Genes GS163065: MP:0005032 abnormal ectoplacental cone morphology
Expand Tier I Mouse MP 7 Genes GS165446: MP:0010315 increased cholangiocarcinoma incidence
Expand Tier I Mouse MP 226 Genes GS162928: MP:0006108 abnormal hindbrain development
Expand Tier I Mouse GO 747 Genes GS193294: GO:0000902 cell morphogenesis
Expand Tier I Mouse GO 1648 Genes GS190954: GO:0009056 catabolic process
Expand Tier I Human GO 865 Genes GS197670: GO:0051247 positive regulation of protein metabolic process
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Mouse MP 360 Genes GS163635: MP:0001933 abnormal litter size
Expand Tier I Mouse GO 1628 Genes GS177813: GO:0031974 membrane-enclosed lumen
Expand Tier I Mouse GO 370 Genes GS193610: GO:0007389 pattern specification process
Expand Tier I Human GO 73 Genes GS194472: GO:0046824 positive regulation of nucleocytoplasmic transport
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 153 Genes GS204929: GO:0042176 regulation of protein catabolic process
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Mouse GO 422 Genes GS183109: GO:0034622 cellular macromolecular complex assembly
Expand Tier I Human GO 349 Genes GS198204: GO:0032880 regulation of protein localization
Expand Tier I Human GO 38 Genes GS194462: GO:0010717 regulation of epithelial to mesenchymal transition
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Mouse GO 53 Genes GS182881: GO:0014033 neural crest cell differentiation
Expand Tier I Mouse GO 2982 Genes GS183514: GO:0019219 regulation of nucleobase-containing compound metabolic process
Expand Tier I Mouse GO 5650 Genes GS183848: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Mouse GO 2855 Genes GS186757: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Mouse MP 969 Genes GS164257: MP:0002085 abnormal embryonic tissue morphology
Expand Tier I Mouse MP 1051 Genes GS166825: MP:0000462 abnormal digestive system morphology
Expand Tier I Mouse MP 141 Genes GS169966: MP:0001219 thick epidermis
Expand Tier I Mouse GO 168 Genes GS178904: GO:0061138 morphogenesis of a branching epithelium
Expand Tier I Mouse GO 198 Genes GS182702: GO:0051170 nuclear import
Expand Tier I Mouse GO 1212 Genes GS180878: GO:0051246 regulation of protein metabolic process
Expand Tier I Mouse GO 880 Genes GS186179: GO:0045934 negative regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 16 Genes GS176677: HP:0100273 Neoplasm of the colon
Expand Tier I Mouse MP 115 Genes GS165857: MP:0000527 abnormal kidney development
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Mouse MP 1724 Genes GS164220: MP:0002882 abnormal neuron morphology
Expand Tier I Human GO 3121 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 250 Genes GS206757: GO:0072001 renal system development
Expand Tier I Mouse MP 610 Genes GS170086: MP:0000703 abnormal thymus morphology
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Mouse GO 1435 Genes GS190397: GO:0032879 regulation of localization
Expand Tier I Mouse MP 369 Genes GS170089: MP:0000706 small thymus
Expand Tier I Mouse GO 1088 Genes GS187749: GO:0019220 regulation of phosphate metabolic process
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human GO 421 Genes GS200015: GO:0001816 cytokine production
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Mouse MP 96 Genes GS169577: MP:0010224 abnormal heart ventricle outflow tract morphology
Expand Tier I Mouse GO 189 Genes GS181854: GO:0045926 negative regulation of growth
Expand Tier I Mouse GO 778 Genes GS186526: GO:0005654 nucleoplasm
Expand Tier I Mouse MP 467 Genes GS168549: MP:0000477 abnormal intestine morphology
Expand Tier I Mouse GO 43 Genes GS178242: GO:0001159 core promoter proximal region DNA binding
Expand Tier I Human 51 Genes GS173085: HP:0000490 Deeply set eye
Expand Tier I Mouse GO 3473 Genes GS190950: GO:0009059 macromolecule biosynthetic process
Expand Tier I Mouse GO 1187 Genes GS181568: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human CTD 205 Genes GS123883: Methylnitrosourea interacting genes (MeSH:D008770) in CTD
Expand Tier I Mouse MP 1274 Genes GS164320: MP:0003861 abnormal nervous system development
Expand Tier I Mouse MP 762 Genes GS166154: MP:0011098 complete embryonic lethality during organogenesis
Expand Tier I Mouse GO 13263 Genes GS178461: GO:0009987 cellular process
Expand Tier I Human GO 429 Genes GS210555: GO:0007389 pattern specification process
Expand Tier II Mouse 238 Genes GS84311: high-dose ethanol actions (Published QTL, Chr 18)
Expand Tier I Mouse GO 3 Genes GS177536: GO:0072076 nephrogenic mesenchyme development
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human GO 223 Genes GS205296: GO:0045165 cell fate commitment
Expand Tier I Human 203 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Mouse MP 318 Genes GS166291: MP:0011108 partial embryonic lethality during organogenesis
Expand Tier I Human GO 61 Genes GS197295: GO:0042307 positive regulation of protein import into nucleus
Expand Tier I Mouse MP 1386 Genes GS169973: MP:0002006 tumorigenesis
Expand Tier I Human 68 Genes GS173148: HP:0003712 Muscle hypertrophy
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Mouse GO 2223 Genes GS179830: GO:0006464 cellular protein modification process
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 40 Genes GS188072: GO:0042177 negative regulation of protein catabolic process
Expand Tier I Mouse GO 2678 Genes GS181892: GO:0048523 negative regulation of cellular process
Expand Tier I Mouse MP 47 Genes GS167529: MP:0005184 abnormal circulating progesterone level
Expand Tier I Human 68 Genes GS170786: HP:0010972 Anemia of inadequate production
Expand Tier I Mouse GO 728 Genes GS191792: GO:0070271 protein complex biogenesis
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
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 Mouse MP 223 Genes GS170512: MP:0010680 abnormal skin adnexa physiology
Expand Tier I Human GO 566 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Mouse MP 873 Genes GS165493: MP:0000653 abnormal sex gland morphology
Expand Tier I Mouse MP 349 Genes GS166162: MP:0011090 partial perinatal lethality
Expand Tier I Mouse GO 1 Genes GS185194: GO:0030616 transforming growth factor beta receptor, common-partner cytoplasmic mediator activity
Expand Tier I Human GO 794 Genes GS200986: GO:0032270 positive regulation of cellular protein metabolic process
Expand Tier I Human GO 2317 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Mouse MP 114 Genes GS166127: MP:0001272 increased metastatic potential
Expand Tier I Mouse MP 60 Genes GS170401: MP:0000471 abnormal stomach epithelium morphology
Expand Tier I Human CTD 13 Genes GS124469: S-nitro-N-acetylpenicillamine interacting genes (MeSH:C110881) in CTD
Expand Tier I Mouse MP 81 Genes GS170069: MP:0002718 abnormal inner cell mass morphology
Expand Tier I Human 374 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 10 Genes GS209407: GO:0005072 transforming growth factor beta receptor, cytoplasmic mediator activity
Expand Tier I Mouse MP 371 Genes GS163051: MP:0000267 abnormal heart development
Expand Tier I Human 29 Genes GS174519: HP:0009145 Abnormalities of the cerebral arteries
Expand Tier I Human GO 10 Genes GS200865: GO:0060391 positive regulation of SMAD protein import into nucleus
Expand Tier I Mouse GO 687 Genes GS188291: GO:0009967 positive regulation of signal transduction
Expand Tier I Human GO 263 Genes GS197298: GO:0042303 molting cycle
Expand Tier I Mouse MP 31 Genes GS169897: MP:0009220 prostate gland adenocarcinoma
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Mouse GO 766 Genes GS186442: GO:0071822 protein complex subunit organization
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Mouse GO 285 Genes GS178973: GO:0022604 regulation of cell morphogenesis
Expand Tier I Mouse MP 443 Genes GS163419: MP:0009209 abnormal internal female genitalia morphology
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 28 Genes GS174853: HP:0000946 Hypoplastic ilia
Expand Tier I Mouse MP 201 Genes GS163263: MP:0003762 abnormal immune organ physiology
Expand Tier I Mouse GO 82 Genes GS184457: GO:0009895 negative regulation of catabolic process
Expand Tier I Mouse MP 829 Genes