Gene Details



SMAD4 and homologs in 1 species are found in 806 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 Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
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 Human GO 1050 Genes GS202082: GO:0051254 positive regulation of RNA metabolic process
Expand Tier I Human 99 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human GO 279 Genes GS206188: GO:0048589 developmental growth
Expand Tier I Human GO 20 Genes GS197033: GO:0030511 positive regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human 16 Genes GS176677: HP:0100273 Neoplasm of the colon
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 Human GO 195 Genes GS206380: GO:0001763 morphogenesis of a branching structure
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 Human GO 7638 Genes GS201949: GO:0044699 single-organism 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 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 Human GO 1171 Genes GS203018: GO:0045935 positive regulation of nucleobase-containing compound metabolic process
Expand Human 1339 Genes GS219979: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Human 150 Genes GS221235: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Human 51 Genes GS173085: HP:0000490 Deeply set eye
Expand Tier I Human CTD 205 Genes GS123883: Methylnitrosourea interacting genes (MeSH:D008770) in CTD
Expand Tier I Human 99 Genes GS173687: HP:0001643 Patent ductus arteriosus
Expand Tier I Human GO 429 Genes GS210555: GO:0007389 pattern specification process
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 Human GO 2940 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human GO 161 Genes GS207039: GO:0060485 mesenchyme development
Expand Tier I Human 181 Genes GS175391: HP:0011004 Abnormality of the systemic arterial tree
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human GO 23 Genes GS200184: GO:0010718 positive regulation of epithelial to mesenchymal transition
Expand Tier I Human GO 1336 Genes GS200555: GO:0010605 negative regulation of macromolecule metabolic process
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 61 Genes GS197295: GO:0042307 positive regulation of protein import into nucleus
Expand Tier I Human 150 Genes GS174586: HP:0005930 Abnormality of the epiphyses
Expand Human 105 Genes GS220967: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_OOCYTE_MEIOSIS
Expand Human 1661 Genes GS219981: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
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 Human GO 104 Genes GS195417: GO:0005057 receptor signaling protein activity
Expand Tier I Human GO 88 Genes GS199902: GO:0090316 positive regulation of intracellular protein transport
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 68 Genes GS170786: HP:0010972 Anemia of inadequate production
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 Human 1985 Genes GS219980: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 566 Genes GS194646: GO:0042803 protein homodimerization activity
Expand Tier I Human GO 910 Genes GS202930: GO:2000113 negative regulation of cellular macromolecule biosynthetic process
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 Human CTD 13 Genes GS124469: S-nitro-N-acetylpenicillamine interacting genes (MeSH:C110881) in CTD
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 104 Genes GS176638: HP:0011603 Congenital malformation of the great arteries
Expand Tier I Human GO 10 Genes GS209407: GO:0005072 transforming growth factor beta receptor, cytoplasmic mediator activity
Expand Tier I Human CTD 2780 Genes GS123332: 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide interacting genes (MeSH:D015123) in CTD
Expand Tier I Human 29 Genes GS174519: HP:0009145 Abnormalities of the cerebral arteries
Expand Tier I Human 198 Genes GS175538: HP:0011276 Vascular skin abnormality
Expand Tier I Human GO 10 Genes GS200865: GO:0060391 positive regulation of SMAD protein import into nucleus
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 Human GO 40 Genes GS204930: GO:0042177 negative regulation of protein catabolic process
Expand Tier I Human GO 2719 Genes GS199273: GO:0043233 organelle lumen
Expand Tier I Human GO 263 Genes GS197298: GO:0042303 molting cycle
Expand Human 181 Genes GS220151: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CHEMOKINE_SIGNALING_PATHWAY
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 Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human CTD 111 Genes GS122521: Nitric Oxide interacting genes (MeSH:D009569) in CTD
Expand Tier I Human 28 Genes GS174853: HP:0000946 Hypoplastic ilia
Expand Tier I Human GO 187 Genes GS197672: GO:0010769 regulation of cell morphogenesis involved in differentiation
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 1287 Genes GS205610: GO:0044430 cytoskeletal part
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 GO 1559 Genes GS201869: GO:0008104 protein localization
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human CTD 1201 Genes GS123595: Progesterone interacting genes (MeSH:D011374) in CTD
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human GO 56 Genes GS203397: GO:0007492 endoderm development
Expand Tier I Human 43 Genes GS173159: HP:0002239 Gastrointestinal hemorrhage
Expand Tier I Human 89 Genes GS174323: HP:0004414 Abnormality of the pulmonary artery
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human CTD 13 Genes GS123829: dimethylthioarsinic acid interacting genes (MeSH:C547156) in CTD
Expand Tier I Human CTD 85 Genes GS125731: nitrofen interacting genes (MeSH:C007350) in CTD
Expand Human 83 Genes GS219676: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_DILATED_CARDIOMYOPATHY
Expand Tier I Human GO 300 Genes GS195731: GO:0022604 regulation of cell morphogenesis
Expand Human 1985 Genes GS219986: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 44 Genes GS175611: HP:0002092 Pulmonary hypertension
Expand Tier I Human 30 Genes GS172647: HP:0011867 Abnormality of the wing of the ilium
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Human 125 Genes GS174854: HP:0001410 Decreased liver function
Expand Tier I Human GO 1084 Genes GS206191: GO:0048584 positive regulation of response to stimulus
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Human 1985 Genes GS219964: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human CTD 2013 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human GO 2896 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human 23 Genes GS174583: HP:0002034 Abnormality of the rectum
Expand Tier I Human GO 156 Genes GS207473: GO:0033157 regulation of intracellular protein transport
Expand Tier I Human GO 938 Genes GS210237: GO:0000902 cell morphogenesis
Expand Tier I Human GO 2033 Genes GS201132: GO:0010646 regulation of cell communication
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human GO 206 Genes GS196231: GO:0001822 kidney development
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 72 Genes GS175808: HP:0011028 Abnormality of blood circulation
Expand Tier I Human 35 Genes GS175326: HP:0001217 Clubbing
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 Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 283 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human GO 208 Genes GS201404: GO:0009952 anterior/posterior pattern specification
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 3917 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 163 Genes GS206933: GO:0051222 positive regulation of protein transport
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 32 Genes GS176916: HP:0004437 Cranial hyperostosis
Expand Tier I Human GO 2 Genes GS203820: GO:0072134 nephrogenic mesenchyme morphogenesis
Expand Tier I Human 27 Genes GS175940: HP:0100834 Neoplasm of the large intestine
Expand Human 1661 Genes GS219738: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 1010 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 7 Genes GS172525: HP:0001698 Pericardial effusion
Expand Tier I Human GO 165 Genes GS210361: GO:0090092 regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human GO 2098 Genes GS209551: GO:0031981 nuclear lumen
Expand Human 105 Genes GS219650: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_OOCYTE_MEIOSIS
Expand Tier I Human GO 37 Genes GS206690: GO:0060389 pathway-restricted SMAD protein phosphorylation
Expand Tier I Human GO 2764 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human GO 200 Genes GS202527: GO:0032386 regulation of intracellular transport
Expand Tier I Human CTD 578 Genes GS123943: Curcumin interacting genes (MeSH:D003474) 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 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 157 Genes GS176612: HP:0000272 Malar flattening
Expand Tier I Human GO 3573 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 298 Genes GS199757: GO:0035239 tube morphogenesis
Expand Tier I Human GO 109 Genes GS199937: GO:0030509 BMP signaling pathway
Expand Tier I Human GO 140 Genes GS200808: GO:0048762 mesenchymal cell differentiation
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 7 Genes GS173699: HP:0007420 Spontaneous hematomas
Expand Tier I Human 177 Genes GS173048: HP:0005557 Abnormality of the zygomatic arch
Expand Tier I Human GO 1639 Genes GS204106: GO:0060089 molecular transducer activity
Expand Tier I Human GO 899 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human 39 Genes GS174016: HP:0000717 Autism
Expand Tier I Human GO 1008 Genes GS204232: GO:0001071 nucleic acid binding transcription factor activity
Expand Tier I Human GO 290 Genes GS206898: GO:0001655 urogenital system development
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human GO 310 Genes GS194560: GO:0043623 cellular protein complex assembly
Expand Tier I Human 15 Genes GS172765: HP:0001680 Coarctation of aorta
Expand Human 1339 Genes GS219985: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human GO 754 Genes GS201131: GO:0010647 positive regulation of cell communication
Expand Tier I Human 41 Genes GS174482: HP:0010579 Cone-shaped epiphysis
Expand Tier I Human 45 Genes GS174144: HP:0002867 Abnormality of the ilium
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 223 Genes GS176632: HP:0001903 Anemia
Expand Tier I Human 57 Genes GS176765: HP:0001009 Telangiectasia
Expand Tier I Human 115 Genes GS170850: HP:0006265 Aplasia/Hypoplasia of fingers
Expand Tier I Human GO 921 Genes GS203019: GO:0045934 negative regulation of nucleobase-containing compound metabolic process
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 806 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human GO 1770 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 1004 Genes GS198240: GO:0031399 regulation of protein modification process
Expand Tier I Human GO 682 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 49 Genes GS173990: HP:0000502 Abnormality of the conjunctiva
Expand Tier I Human 72 Genes GS175809: HP:0011029 Internal hemorrhage
Expand Tier I Human GO 1393 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human GO 19 Genes GS207485: GO:0071604 transforming growth factor beta production
Expand Tier I Human 10 Genes GS176350: HP:0100833 Neoplasm of the small intestine
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human GO 597 Genes GS199620: GO:0060429 epithelium development
Expand Tier I Human GO 71 Genes GS206244: GO:0090100 positive regulation of transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
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 2332 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human GO 1842 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Human 968 Genes GS221018: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
Expand Tier I Human 102 Genes GS177035: HP:0001928 Abnormality of coagulation
Expand Tier I Human GO 1096 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human GO 306 Genes GS209956: GO:0003002 regionalization
Expand Tier I Human 33 Genes GS171455: HP:0008772 Aplasia/Hypoplasia of the external ear
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 Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 336 Genes GS196532: GO:0000975 regulatory region DNA binding
Expand Tier I Human GO 89 Genes GS193946: GO:0017015 regulation of transforming growth factor beta receptor signaling pathway
Expand Tier I Human GO 8 Genes GS205524: GO:0032525 somite rostral/caudal axis specification
Expand Tier I Human GO 213 Genes GS199498: GO:0051170 nuclear import
Expand Tier I Human GO 33 Genes GS197002: GO:0071559 response to transforming growth factor beta stimulus
Expand Tier I Human GO 466 Genes GS204511: GO:0048729 tissue morphogenesis
Expand Tier I Human 3 Genes GS175307: HP:0006548 Pulmonary arteriovenous malformation
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Human 105 Genes GS220169: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_OOCYTE_MEIOSIS
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 1256 Genes GS210178: GO:0031328 positive regulation of cellular biosynthetic process
Expand Tier I Human 17 Genes GS173461: HP:0001650 Aortic valve stenosis
Expand Tier I Human GO 11 Genes GS203299: GO:0007183 SMAD protein complex assembly
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 67 Genes GS172676: HP:0002250 Abnormality of the large intestine
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 1214 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Human 1417 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 Human GO 1412 Genes GS197669: GO:0051246 regulation of protein metabolic process
Expand Tier I Human GO 1972 Genes GS210586: GO:0051641 cellular localization
Expand Tier I Human GO 7 Genes GS210684: GO:0032909 regulation of transforming growth factor beta2 production
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 1198 Genes GS199501: GO:0051173 positive regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1815 Genes GS208187: GO:0010033 response to organic substance
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 433 Genes GS207210: GO:0035295 tube development
Expand Tier I Human GO 295 Genes GS194908: GO:0001558 regulation of cell growth
Expand Tier I Human GO 1 Genes GS202009: GO:0030616 transforming growth factor beta receptor, common-partner cytoplasmic mediator activity
Expand Tier I Human 12 Genes GS170954: HP:0000885 Broad ribs
Expand Tier I Human GO 14 Genes GS194275: GO:0072075 metanephric mesenchyme development
Expand Tier I Human GO 994 Genes GS196927: GO:0065003 macromolecular complex assembly
Expand Tier I Human 18 Genes GS170977: HP:0001935 Microcytic anemia
Expand Tier I Human 39 Genes GS174048: HP:0000729 Autism spectrum disorder
Expand Tier I Human 56 Genes GS175055: HP:0001080 Biliary tract abnormality
Expand Tier I Human GO 5948 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human GO 863 Genes GS209634: GO:0015630 microtubule cytoskeleton
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human GO 140 Genes GS202933: GO:0030308 negative regulation of cell growth
Expand Tier I Human GO 31 Genes GS205848: GO:0030513 positive regulation of BMP signaling pathway
Expand Tier I Human GO 993 Genes GS209525: GO:0032989 cellular component morphogenesis
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 88 Genes GS206759: GO:0072006 nephron development
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human GO 328 Genes GS202371: GO:0044212 transcription regulatory region DNA binding
Expand Tier I Human 246 Genes GS173534: HP:0001877 Abnormality of erythrocytes
Expand Human 1661 Genes GS219987: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE_PART
Expand Tier I Human 38 Genes GS170846: HP:0010930 Abnormality of monovalent inorganic cation homeostasis
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 Human GO 1175 Genes GS209951: GO:0042127 regulation of cell proliferation
Expand Tier I Human 148 Genes GS172906: HP:0003319 Abnormality of the cervical spine
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 1477 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 67 Genes GS171788: HP:0001394 Cirrhosis
Expand Tier I Human 104 Genes GS173512: HP:0000306 Abnormality of the chin
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 Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 117 Genes GS172364: HP:0003111 Abnormality of ion homeostasis
Expand Tier I Human 39 Genes GS174178: HP:0100774 Hyperostosis
Expand Tier I Human 6 Genes GS174582: HP:0002035 Rectal prolapse
Expand Tier I Human GO 68 Genes GS200104: GO:0060675 ureteric bud morphogenesis
Expand Tier I Human GO 223 Genes GS206323: GO:0034762 regulation of transmembrane transport
Expand Tier I Human 98 Genes GS174851: HP:0000944 Abnormality of the metaphyses
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Human 77 Genes GS222134: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PROGESTERONE_MEDIATED_OOCYTE_MATURATION
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 Human GO 75 Genes GS208713: GO:0001837 epithelial to mesenchymal transition
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 CTD 129 Genes GS124163: Streptozocin interacting genes (MeSH:D013311) in CTD
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 60 Genes GS173119: HP:0002315 Headache
Expand Tier I Human 75 Genes GS175886: HP:0007378 Neoplasm of the gastrointestinal tract
Expand Tier I Human 15 Genes GS171704: HP:0003073 Hypoalbuminemia
Expand Tier I Human GO 168 Genes GS195660: GO:0061138 morphogenesis of a branching epithelium
Expand Human 968 Genes GS219975: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_PLASMA_MEMBRANE
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 Human GO 103 Genes GS206905: GO:0001657 ureteric bud development
Expand Tier I Human GO 7 Genes GS210685: GO:0032906 transforming growth factor beta2 production
Expand Tier I Human 84 Genes GS172316: HP:0003026 Short long bones
Expand Tier I Human 18 Genes GS173403: HP:0002684 Thickened calvaria
Expand Tier I Human 128 Genes GS171035: HP:0002620 Systemic artery abnormality
Expand Tier I Human 19 Genes GS175282: HP:0006749 Malignant gastrointestinal tract tumors
Expand Human 1985 Genes GS219747: http://www.broadinstitute.org/gsea/msigdb/cards/MEMBRANE
Expand Tier I Human 19 Genes GS172152: HP:0002672 Gastrointestinal carcinoma
Expand Tier I Human 61 Genes GS174375: HP:0002027 Abdominal pain
Expand Tier I Human GO 3104 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 4314 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 2486 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 1204 Genes GS204610: GO:0019220 regulation of phosphate metabolic process
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 Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human GO 3626 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 474 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Human 150 Genes GS219668: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PURINE_METABOLISM
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human GO 526 Genes GS208562: GO:0040008 regulation of growth
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
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 22 Genes GS176523: HP:0002900 Hypokalemia
Expand Tier I Human GO 277 Genes GS193992: GO:0048732 gland development
Expand Tier I Human CTD 123 Genes GS125491: Fenofibrate interacting genes (MeSH:D011345) in CTD
Expand Tier I Human GO 3310 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human GO 174 Genes GS198821: GO:0051098 regulation of binding
Expand Human 270 Genes GS222841: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_NEURONAL_SYSTEM
Expand Tier I Human 12 Genes GS175319: HP:0005266 Intestinal polyps
Expand Tier I Human GO 499 Genes GS204077: GO:0033365 protein localization to organelle
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4084 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human GO 2494 Genes GS209235: GO:0006793 phosphorus metabolic process
Expand Tier I Human 268 Genes GS172365: HP:0003110 Abnormality of urine homeostasis
Expand Tier I Human 88 Genes GS173938: HP:0001679 Abnormality of the aorta
Expand Tier I Human 3 Genes GS175820: HP:0002408 Cerebral arteriovenous malformation
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 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 843 Genes GS202079: GO:0051253 negative regulation of RNA metabolic process
Expand Tier I Human GO 1430 Genes GS201262: GO:0009892 negative regulation of metabolic process
Expand Tier I Human CTD 794 Genes GS125548: Doxorubicin interacting genes (MeSH:D004317) in CTD
Expand Tier I Human 17 Genes GS172378: HP:0002866 Hypoplastic iliac wings
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 19 Genes GS203186: GO:0071634 regulation of transforming growth factor beta production
Expand Tier I Human 30 Genes GS175081: HP:0006753 Neoplasm of the stomach
Expand Tier I Human 1 Genes GS176398: HP:0004784 Juvenile gastrointestinal polyposis
Expand Tier I Human GO 493 Genes GS200286: GO:0060284 regulation of cell development
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 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 28 Genes GS202087: GO:0010770 positive regulation of cell morphogenesis involved in differentiation
Expand Tier I Human GO 688 Genes GS203895: GO:0006886 intracellular protein transport
Expand Tier I Human 66 Genes GS174437: HP:0005114 Abnormalities of the peripheral arteries
Expand Tier I Human 5 Genes GS175474: HP:0006771 Duodenal carcinoma
Expand Tier I Human 23 Genes GS171268: HP:0002637 Cerebral ischemia
Expand Tier I Human GO 64 Genes GS206907: GO:0001658 branching involved in ureteric bud morphogenesis
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
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 486 Genes GS208302: GO:0005815 microtubule organizing center
Expand Tier I Human 93 Genes GS170972: HP:0001933 Subcutaneous hemorrhage
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Human 1321 Genes GS219945: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 43 Genes GS173055: HP:0000326 Abnormality of the maxilla
Expand Tier I Human 109 Genes GS174136: HP:0002014 Diarrhea
Expand Tier I Human 63 Genes GS171593: HP:0000160 Narrow mouth
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 339 Genes GS203827: GO:0051169 nuclear transport
Expand Tier I Human GO 484 Genes GS209725: GO:0000122 negative regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Human 77 Genes GS220968: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PROGESTERONE_MEDIATED_OOCYTE_MATURATION
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 8 Genes GS175703: HP:0003003 Colon cancer
Expand Human 1321 Genes GS219984: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human GO 70 Genes GS196572: GO:0060021 palate development
Expand Tier I Human GO 50 Genes GS201433: GO:0005518 collagen binding
Expand Tier I Human GO 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Human 77 Genes GS221217: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PROGESTERONE_MEDIATED_OOCYTE_MATURATION
Expand Tier I Human GO 228 Genes GS204208: GO:0006352 DNA-dependent transcription, initiation
Expand Tier I Human 62 Genes GS173692: HP:0001646 Abnormality of the aortic valve
Expand Tier I Human 96 Genes GS174884: HP:0009381 Short finger
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 7 Genes GS174489: HP:0000524 Conjunctival telangiectasia
Expand Tier I Human CTD 14 Genes GS122878: Doxazosin interacting genes (MeSH:D017292) in CTD
Expand Tier I Human 77 Genes GS174230: HP:0000303 Mandibular prognathia
Expand Tier I Human 4 Genes GS174288: HP:0002576 Intussusception
Expand Tier I Human GO 3487 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1001 Genes GS199986: GO:0009719 response to endogenous stimulus
Expand Tier I Human GO 3446 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 928 Genes GS208787: GO:0034613 cellular protein localization
Expand Tier I Human GO 41 Genes GS197049: GO:0009948 anterior/posterior axis specification
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 Human CTD 4389 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human GO 608 Genes GS195457: GO:0060341 regulation of cellular localization
Expand Tier I Human 236 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human GO 364 Genes GS200690: GO:0002009 morphogenesis of an epithelium
Expand Tier I Human GO 950 Genes GS208067: GO:0010558 negative regulation of macromolecule biosynthetic process
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 11 Genes GS197915: GO:0051797 regulation of hair follicle development
Expand Tier I Human GO 493 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human GO 498 Genes GS196986: GO:0045597 positive regulation of cell differentiation
Expand Human 77 Genes GS220170: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_PROGESTERONE_MEDIATED_OOCYTE_MATURATION
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 Human GO 56 Genes GS204853: GO:0048663 neuron fate commitment
Expand Tier I Human 26 Genes GS176721: HP:0001297 Stroke
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
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 19 Genes GS172514: HP:0001697 Abnormality of the pericardium
Expand Tier I Human GO 1588 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human GO 1263 Genes GS197087: GO:0016310 phosphorylation
Expand Tier I Human GO 257 Genes GS208672: GO:0022404 molting cycle process
Expand Tier I Human GO 84 Genes GS206901: GO:0001656 metanephros development
Expand Tier I Human GO 901 Genes GS209281: GO:0010629 negative regulation of gene expression
Expand Tier I Human 315 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human GO 774 Genes GS208730: GO:0070271 protein complex biogenesis
Expand Human 982 Genes GS219722: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_PLASMA_MEMBRANE
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human GO 1115 Genes GS196587: GO:0006468 protein phosphorylation
Expand Human 1417 Genes GS219983: http://www.broadinstitute.org/gsea/msigdb/cards/PLASMA_MEMBRANE
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Human 181 Genes GS220974: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_CHEMOKINE_SIGNALING_PATHWAY
Expand Tier I Human 52 Genes GS176460: HP:0000790 Hematuria
Expand Tier I Human CTD 241 Genes GS122988: Chlorodiphenyl (54% Chlorine) interacting genes (MeSH:D020111) in CTD
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human 9 Genes GS174786: HP:0002040 Esophageal varices
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 136 Genes GS202418: GO:0007369 gastrulation
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human GO 2875 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 95 Genes GS202521: GO:0032388 positive regulation of intracellular transport
Expand Tier I Human 220 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 38 Genes GS171826: HP:0001977 Abnormal thrombosis
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
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 Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 289 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human GO 73 Genes GS194472: GO:0046824 positive regulation of nucleocytoplasmic transport
Expand Tier I Human GO 280 Genes GS202739: GO:0017038 protein import
Expand Tier I Human GO 3 Genes GS207756: GO:0032444 activin responsive factor complex
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human GO 1179 Genes GS208060: GO:0010557 positive regulation of macromolecule biosynthetic process
Expand Human 1339 Genes GS219731: http://www.broadinstitute.org/gsea/msigdb/cards/INTRINSIC_TO_MEMBRANE
Expand Tier I Human 6 Genes GS174285: HP:0002573 Hematochezia
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human GO 153 Genes GS204929: GO:0042176 regulation of protein catabolic process
Expand Tier I Human GO 33 Genes GS206225: GO:0060393 regulation of pathway-restricted SMAD protein phosphorylation
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human GO 853 Genes GS205416: GO:0042325 regulation of phosphorylation
Expand Human 1321 Genes GS219728: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Human 1321 Genes GS219978: http://www.broadinstitute.org/gsea/msigdb/cards/INTEGRAL_TO_MEMBRANE
Expand Tier I Human GO 689 Genes GS199906: GO:0034621 cellular macromolecular complex subunit organization
Expand Tier I Human GO 110 Genes GS203402: GO:0007498 mesoderm development
Expand Tier I Human 72 Genes GS176835: HP:0000426 Prominent nasal bridge
Expand Tier I Human GO 251 Genes GS201011: GO:0036293 response to decreased oxygen levels