Gene Details



FGF8 and homologs in 1 species are found in 480 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 Human CTD 104 Genes GS124724: Thalidomide interacting genes (MeSH:D013792) in CTD
Expand Tier I Human GO 91 Genes GS197114: GO:0043524 negative regulation of neuron apoptotic process
Expand Tier I Human GO 40 Genes GS206966: GO:0001974 blood vessel remodeling
Expand Tier I Human 270 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human GO 26 Genes GS210425: GO:0048854 brain morphogenesis
Expand Tier I Human GO 195 Genes GS206380: GO:0001763 morphogenesis of a branching structure
Expand Tier I Human GO 3108 Genes GS198685: GO:0048522 positive regulation of cellular process
Expand Tier I Human GO 248 Genes GS206757: GO:0072001 renal system development
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Human 1715 Genes GS221148: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 274 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 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Human 1715 Genes GS221397: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human GO 109 Genes GS206173: GO:0035113 embryonic appendage morphogenesis
Expand Tier I Human GO 688 Genes GS210376: GO:0007417 central nervous system development
Expand Tier I Human GO 3304 Genes GS210180: GO:0031326 regulation of cellular biosynthetic process
Expand Tier I Human GO 429 Genes GS210555: GO:0007389 pattern specification process
Expand Tier I Human GO 12 Genes GS201222: GO:0030917 midbrain-hindbrain boundary development
Expand Tier I Human 55 Genes GS173418: HP:0000144 Decreased fertility
Expand Tier I Human GO 47 Genes GS199134: GO:0035272 exocrine system development
Expand Tier I Human GO 222 Genes GS205296: GO:0045165 cell fate commitment
Expand Tier I Human CTD 18 Genes GS125830: Heparitin Sulfate interacting genes (MeSH:D006497) in CTD
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 3334 Genes GS205622: GO:0009889 regulation of biosynthetic process
Expand Tier I Human GO 652 Genes GS208657: GO:0008284 positive regulation of cell proliferation
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human GO 161 Genes GS207039: GO:0060485 mesenchyme development
Expand Tier I Human GO 1066 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 329 Genes GS198056: GO:0048568 embryonic organ development
Expand Tier I Human GO 59 Genes GS202299: GO:0051781 positive regulation of cell division
Expand Tier I Human GO 1079 Genes GS209282: GO:0010628 positive regulation of gene expression
Expand Tier I Human GO 165 Genes GS208659: GO:0008286 insulin receptor signaling pathway
Expand Tier I Human GO 21 Genes GS209576: GO:0072132 mesenchyme morphogenesis
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human GO 200 Genes GS200597: GO:0008406 gonad development
Expand Tier I Human GO 133 Genes GS197707: GO:0016331 morphogenesis of embryonic epithelium
Expand Tier I Human GO 846 Genes GS203276: GO:0007243 intracellular protein kinase cascade
Expand Tier I Human GO 45 Genes GS204187: GO:0021983 pituitary gland development
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human GO 59 Genes GS197824: GO:0001707 mesoderm formation
Expand Tier I Human GO 3180 Genes GS208061: GO:0010556 regulation of macromolecule biosynthetic process
Expand Tier I Human GO 57 Genes GS198146: GO:0003279 cardiac septum development
Expand Tier I Human GO 5 Genes GS193994: GO:0005105 type 1 fibroblast growth factor receptor binding
Expand Tier I Human GO 721 Genes GS204317: GO:0009725 response to hormone stimulus
Expand Tier I Human GO 96 Genes GS200125: GO:0070851 growth factor receptor binding
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human GO 2308 Genes GS209215: GO:0007166 cell surface receptor signaling pathway
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human GO 580 Genes GS199789: GO:0043069 negative regulation of programmed cell death
Expand Tier I Human GO 2653 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human GO 1098 Genes GS195083: GO:0007267 cell-cell signaling
Expand Tier I Human 372 Genes GS175815: HP:0011025 Abnormality of cardiovascular system physiology
Expand Tier I Human GO 490 Genes GS202261: GO:0001568 blood vessel development
Expand Tier I Human GO 1174 Genes GS207161: GO:0006928 cellular component movement
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 48 Genes GS199612: GO:0061371 determination of heart left/right asymmetry
Expand Tier I Human GO 84 Genes GS194721: GO:0035265 organ growth
Expand Tier I Human GO 91 Genes GS208230: GO:1901215 negative regulation of neuron death
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human GO 598 Genes GS201231: GO:0060548 negative regulation of cell death
Expand Tier I Human GO 35 Genes GS202490: GO:0090130 tissue migration
Expand Tier I Human CTD 163 Genes GS123134: Forskolin interacting genes (MeSH:D005576) in CTD
Expand Tier I Human GO 260 Genes GS195560: GO:0007548 sex differentiation
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 16 Genes GS200354: GO:0045843 negative regulation of striated muscle tissue development
Expand Tier I Human GO 3 Genes GS202348: GO:0048382 mesendoderm development
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human CTD 528 Genes GS125792: Ethanol interacting genes (MeSH:D000431) in CTD
Expand Tier I Human GO 15 Genes GS205346: GO:0021903 rostrocaudal neural tube patterning
Expand Tier I Human GO 145 Genes GS208229: GO:1901214 regulation of neuron death
Expand Tier I Human 530 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human GO 465 Genes GS198663: GO:0051301 cell division
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 56 Genes GS203397: GO:0007492 endoderm development
Expand Tier I Human GO 128 Genes GS199683: GO:0014031 mesenchymal cell development
Expand Tier I Human GO 264 Genes GS200030: GO:0032868 response to insulin stimulus
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 96 Genes GS195460: GO:0060348 bone development
Expand Tier I Human GO 4575 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 851 Genes GS203972: GO:0005615 extracellular space
Expand Tier I Human GO 433 Genes GS203054: GO:0048514 blood vessel morphogenesis
Expand Tier I Human GO 169 Genes GS209954: GO:0003007 heart morphogenesis
Expand Tier I Human GO 4354 Genes GS210182: GO:0031323 regulation of cellular metabolic process
Expand Tier I Human GO 34 Genes GS202262: GO:0001569 patterning of blood vessels
Expand Tier I Human GO 1533 Genes GS196282: GO:0012501 programmed cell death
Expand Tier I Human GO 654 Genes GS205165: GO:0010243 response to organic nitrogen
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 39 Genes GS172454: HP:0100335 Non-midline cleft lip
Expand Tier I Human GO 25 Genes GS202730: GO:0003197 endocardial cushion development
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 445 Genes GS200490: GO:0061061 muscle structure development
Expand Tier I Human GO 20 Genes GS203298: GO:0021871 forebrain regionalization
Expand Tier I Human GO 6 Genes GS207964: GO:0007509 mesoderm migration involved in gastrulation
Expand Tier I Human GO 130 Genes GS210596: GO:0035107 appendage morphogenesis
Expand Tier I Human GO 95 Genes GS202297: GO:0051783 regulation of nuclear division
Expand Tier I Human GO 102 Genes GS198438: GO:0048634 regulation of muscle organ development
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human GO 2878 Genes GS206108: GO:2001141 regulation of RNA biosynthetic process
Expand Tier I Human GO 782 Genes GS208559: GO:0040007 growth
Expand Tier I Human GO 936 Genes GS210237: GO:0000902 cell morphogenesis
Expand Tier I Human GO 2816 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human GO 154 Genes GS195637: GO:0030324 lung development
Expand Tier I Human GO 204 Genes GS196231: GO:0001822 kidney development
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human GO 366 Genes GS193838: GO:0000280 nuclear division
Expand Tier I Human GO 67 Genes GS205633: GO:0021536 diencephalon development
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human GO 4 Genes GS194791: GO:0060129 thyroid-stimulating hormone-secreting cell differentiation
Expand Tier I Human GO 516 Genes GS194493: GO:0001944 vasculature development
Expand Tier I Human 886 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 45 Genes GS174869: HP:0000551 Abnormality of color vision
Expand Tier I Human GO 37 Genes GS203325: GO:0003156 regulation of organ formation
Expand Tier I Human CTD 45 Genes GS121638: SU 5402 interacting genes (MeSH:C105686) in CTD
Expand Tier I Human GO 52 Genes GS196771: GO:0048645 organ formation
Expand Tier I Human GO 156 Genes GS195919: GO:0051402 neuron apoptotic process
Expand Tier I Human GO 95 Genes GS197513: GO:0042472 inner ear morphogenesis
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human 73 Genes GS171188: HP:0000415 Abnormality of the choanae
Expand Tier I Human GO 3300 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 16 Genes GS207202: GO:0046622 positive regulation of organ growth
Expand Tier I Human GO 208 Genes GS201404: GO:0009952 anterior/posterior pattern specification
Expand Tier I Human 590 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 109 Genes GS195638: GO:0030326 embryonic limb morphogenesis
Expand Tier I Human GO 142 Genes GS196756: GO:0043523 regulation of neuron apoptotic process
Expand Tier I Human GO 4787 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human GO 199 Genes GS204891: GO:0010638 positive regulation of organelle organization
Expand Tier I Human GO 17 Genes GS201785: GO:0021544 subpallium development
Expand Tier I Human GO 5 Genes GS206977: GO:0021798 forebrain dorsal/ventral pattern formation
Expand Tier I Human GO 146 Genes GS198648: GO:0045927 positive regulation of growth
Expand Tier I Human GO 1 Genes GS202486: GO:0090134 cell migration involved in mesendoderm migration
Expand Tier I Human GO 62 Genes GS205128: GO:0035050 embryonic heart tube development
Expand Tier I Human 46 Genes GS172542: HP:0000830 Anterior hypopituitarism
Expand Tier I Human GO 2939 Genes GS202080: GO:0051252 regulation of RNA metabolic process
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human CTD 56 Genes GS126892: Androgens interacting genes (MeSH:D000728) in CTD
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human GO 12 Genes GS201340: GO:0071542 dopaminergic neuron differentiation
Expand Tier I Human GO 985 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human GO 4 Genes GS204184: GO:0008078 mesodermal cell migration
Expand Tier I Human GO 24 Genes GS201293: GO:0042481 regulation of odontogenesis
Expand Tier I Human GO 1977 Genes GS204568: GO:0009893 positive regulation of metabolic process
Expand Tier I Human GO 64 Genes GS207200: GO:0046620 regulation of organ growth
Expand Tier I Human 113 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Human 1472 Genes GS219991: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human GO 5 Genes GS204527: GO:0005111 type 2 fibroblast growth factor receptor binding
Expand Tier I Human GO 130 Genes GS209937: GO:0035108 limb morphogenesis
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human GO 157 Genes GS195636: GO:0030323 respiratory tube development
Expand Tier I Human GO 139 Genes GS194628: GO:0008543 fibroblast growth factor receptor signaling pathway
Expand Tier I Human CTD 160 Genes GS126498: Dextroamphetamine interacting genes (MeSH:D003913) in CTD
Expand Tier I Human 236 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human GO 406 Genes GS207287: GO:0032870 cellular response to hormone stimulus
Expand Tier I Human 542 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 287 Genes GS202974: GO:0071375 cellular response to peptide hormone stimulus
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human GO 29 Genes GS200614: GO:0035116 embryonic hindlimb morphogenesis
Expand Tier I Human 238 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human GO 315 Genes GS194204: GO:0007346 regulation of mitotic cell cycle
Expand Tier I Human GO 119 Genes GS195315: GO:0046546 development of primary male sexual characteristics
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 Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 275 Genes GS207295: GO:0071363 cellular response to growth factor stimulus
Expand Tier I Human GO 140 Genes GS193995: GO:0048736 appendage development
Expand Tier I Human GO 848 Genes GS208675: GO:0022403 cell cycle phase
Expand Tier I Human 69 Genes GS176623: HP:0000453 Choanal atresia
Expand Tier I Human GO 591 Genes GS195737: GO:0022603 regulation of anatomical structure morphogenesis
Expand Tier I Human GO 435 Genes GS197802: GO:0007423 sensory organ development
Expand Tier I Human GO 19 Genes GS197566: GO:0035909 aorta morphogenesis
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 GO 295 Genes GS201883: GO:0070848 response to growth factor stimulus
Expand Tier I Human CTD 30 Genes GS125315: Heparin interacting genes (MeSH:D006493) in CTD
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Human GO 216 Genes GS198051: GO:0048562 embryonic organ morphogenesis
Expand Tier I Human CTD 6 Genes GS126304: citral interacting genes (MeSH:C007076) in CTD
Expand Tier I Human GO 898 Genes GS201125: GO:0009790 embryo development
Expand Tier I Human GO 288 Genes GS206898: GO:0001655 urogenital system development
Expand Tier I Human GO 335 Genes GS194775: GO:0007517 muscle organ development
Expand Tier I Human GO 30 Genes GS202488: GO:0090132 epithelium migration
Expand Tier I Human GO 50 Genes GS207701: GO:0003143 embryonic heart tube morphogenesis
Expand Tier I Human GO 13 Genes GS201223: GO:0030916 otic vesicle formation
Expand Tier I Human GO 34 Genes GS210373: GO:0007435 salivary gland morphogenesis
Expand Tier I Human GO 48 Genes GS203320: GO:0003151 outflow tract morphogenesis
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 26 Genes GS199563: GO:0021846 cell proliferation in forebrain
Expand Tier I Human GO 136 Genes GS202180: GO:0035270 endocrine system development
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 1164 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Human 576 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human GO 110 Genes GS200141: GO:0001667 ameboidal cell migration
Expand Tier I Human GO 36 Genes GS200353: GO:0045840 positive regulation of mitosis
Expand Tier I Human GO 8 Genes GS202736: GO:0003198 epithelial to mesenchymal transition involved in endocardial cushion formation
Expand Tier I Human GO 27 Genes GS198886: GO:0010092 specification of organ identity
Expand Tier I Human GO 680 Genes GS205338: GO:0051094 positive regulation of developmental process
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1430 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human GO 1241 Genes GS196080: GO:0040011 locomotion
Expand Tier I Human GO 124 Genes GS210335: GO:0048771 tissue remodeling
Expand Tier I Human GO 1533 Genes GS208664: GO:0008283 cell proliferation
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human GO 1391 Genes GS193937: GO:0006366 transcription from RNA polymerase II promoter
Expand Tier I Human GO 24 Genes GS208938: GO:0060445 branching involved in salivary gland morphogenesis
Expand Tier I Human GO 1155 Genes GS206237: GO:0042981 regulation of apoptotic process
Expand Tier I Human GO 181 Genes GS200373: GO:0060070 canonical Wnt receptor signaling pathway
Expand Tier I Human GO 1212 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 904 Genes GS206715: GO:0051674 localization of cell
Expand Tier I Human GO 271 Genes GS196165: GO:0048608 reproductive structure development
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human GO 595 Genes GS199620: GO:0060429 epithelium development
Expand Tier I Human GO 1516 Genes GS194172: GO:0006915 apoptotic process
Expand Tier I Human GO 1 Genes GS202487: GO:0090133 mesendoderm migration
Expand Tier I Human GO 89 Genes GS208306: GO:0061351 neural precursor cell proliferation
Expand Tier I Human GO 267 Genes GS204628: GO:0007178 transmembrane receptor protein serine/threonine kinase signaling pathway
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 95 Genes GS200199: GO:0007088 regulation of mitosis
Expand Tier I Human GO 1197 Genes GS201696: GO:0010941 regulation of cell death
Expand Tier I Human GO 302 Genes GS195143: GO:0016055 Wnt receptor signaling pathway
Expand Tier I Human GO 1839 Genes GS198572: GO:0010604 positive regulation of macromolecule metabolic process
Expand Tier I Human GO 51 Genes GS204715: GO:0060840 artery development
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human GO 177 Genes GS201227: GO:0060541 respiratory system development
Expand Tier I Human GO 1095 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human GO 2104 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human GO 306 Genes GS209956: GO:0003002 regionalization
Expand Tier I Human GO 390 Genes GS194294: GO:0048285 organelle fission
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human GO 215 Genes GS200028: GO:0032869 cellular response to insulin stimulus
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human GO 25 Genes GS202816: GO:0001759 organ induction
Expand Tier I Human GO 165 Genes GS198581: GO:0021537 telencephalon development
Expand Tier I Human GO 466 Genes GS204511: GO:0048729 tissue morphogenesis
Expand Tier I Human GO 1596 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 1541 Genes GS202468: GO:0070887 cellular response to chemical stimulus
Expand Tier I Human GO 366 Genes GS206882: GO:0007067 mitosis
Expand Tier I Human GO 3099 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 779 Genes GS195541: GO:0000278 mitotic cell cycle
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 753 Genes GS204108: GO:0072358 cardiovascular system development
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 2828 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 258 Genes GS206111: GO:0097285 cell-type specific apoptotic process
Expand Tier I Human GO 1214 Genes GS198360: GO:0006357 regulation of transcription from RNA polymerase II promoter
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 182 Genes GS204087: GO:0043583 ear development
Expand Tier I Human GO 1591 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human GO 535 Genes GS205331: GO:0051093 negative regulation of developmental process
Expand Tier I Human GO 43 Genes GS195886: GO:0060411 cardiac septum morphogenesis
Expand Tier I Human GO 3 Genes GS201931: GO:0060128 corticotropin hormone secreting cell differentiation
Expand Tier I Human GO 82 Genes GS208682: GO:0051302 regulation of cell division
Expand Tier I Human CTD 1069 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Human GO 145 Genes GS208717: GO:2000027 regulation of organ morphogenesis
Expand Human 1715 Genes GS222093: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human GO 38 Genes GS208586: GO:0007431 salivary gland development
Expand Tier I Human GO 357 Genes GS209923: GO:0001525 angiogenesis
Expand Tier I Human GO 279 Genes GS195069: GO:0030900 forebrain development
Expand Tier I Human GO 1809 Genes GS208187: GO:0010033 response to organic substance
Expand Tier I Human GO 15 Genes GS207487: GO:0071600 otic vesicle morphogenesis
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human GO 162 Genes GS196633: GO:0070997 neuron death
Expand Tier I Human GO 4129 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 21 Genes GS194095: GO:0030878 thyroid gland development
Expand Tier I Human GO 432 Genes GS207210: GO:0035295 tube development
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human GO 561 Genes GS194647: GO:0071495 cellular response to endogenous stimulus
Expand Tier I Human GO 110 Genes GS194320: GO:0003205 cardiac chamber development
Expand Tier I Human GO 154 Genes GS204804: GO:0071774 response to fibroblast growth factor stimulus
Expand Tier I Human GO 4085 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 18 Genes GS207869: GO:0060317 cardiac epithelial to mesenchymal transition
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 157 Genes GS201548: GO:0048754 branching morphogenesis of a tube
Expand Tier I Human GO 18 Genes GS208645: GO:0048635 negative regulation of muscle organ development
Expand Tier I Human GO 991 Genes GS209525: GO:0032989 cellular component morphogenesis
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Human 1472 Genes GS221269: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human GO 424 Genes GS209955: GO:0003006 developmental process involved in reproduction
Expand Tier I Human GO 570 Genes GS199782: GO:0043066 negative regulation of apoptotic process
Expand Tier I Human GO 8 Genes GS198768: GO:0001839 neural plate morphogenesis
Expand Tier I Human GO 92 Genes GS201403: GO:0009953 dorsal/ventral pattern formation
Expand Tier I Human GO 161 Genes GS207097: GO:0008083 growth factor activity
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human GO 91 Genes GS194159: GO:0009799 specification of symmetry
Expand Tier I Human GO 21 Genes GS201103: GO:0035904 aorta development
Expand Tier I Human GO 2734 Genes GS195668: GO:0042221 response to chemical stimulus
Expand Tier I Human GO 16 Genes GS204190: GO:0021984 adenohypophysis development
Expand Human 1472 Genes GS221020: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human GO 11 Genes GS206674: GO:0003272 endocardial cushion formation
Expand Tier I Human GO 508 Genes GS209105: GO:0000165 MAPK cascade
Expand Tier I Human GO 1170 Genes GS209951: GO:0042127 regulation of cell proliferation
Expand Tier I Human GO 103 Genes GS197516: GO:0042476 odontogenesis
Expand Tier I Human GO 44 Genes GS200692: GO:0048844 artery morphogenesis
Expand Tier I Human GO 36 Genes GS202302: GO:0051785 positive regulation of nuclear division
Expand Tier I Human GO 158 Genes GS207259: GO:0090068 positive regulation of cell cycle process
Expand Tier I Human 141 Genes GS172281: HP:0000822 Hypertension
Expand Tier I Human GO 47 Genes GS200110: GO:0048806 genitalia development
Expand Tier I Human CTD 108 Genes GS123744: Flutamide interacting genes (MeSH:D005485) in CTD
Expand Tier I Human GO 1378 Genes GS209190: GO:0007049 cell cycle
Expand Tier I Human GO 68 Genes GS200104: GO:0060675 ureteric bud morphogenesis
Expand Tier I Human CTD 183 Genes GS125960: Cholecalciferol interacting genes (MeSH:D002762) in CTD
Expand Tier I Human GO 501 Genes GS197801: GO:0007420 brain development
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 75 Genes GS208713: GO:0001837 epithelial to mesenchymal transition
Expand Tier I Human GO 38 Genes GS197485: GO:0035137 hindlimb morphogenesis
Expand Tier I Human GO 377 Genes GS209245: GO:0000087 M phase of mitotic cell cycle
Expand Tier I Human GO 14 Genes GS203921: GO:0042074 cell migration involved in gastrulation
Expand Tier I Human GO 20 Genes GS196394: GO:0071599 otic vesicle development
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 835 Genes GS205758: GO:0016477 cell migration
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 168 Genes GS195660: GO:0061138 morphogenesis of a branching epithelium
Expand Tier I Human GO 39 Genes GS210446: GO:0031128 developmental induction
Expand Tier I Human GO 429 Genes GS195596: GO:0010564 regulation of cell cycle process
Expand Tier I Human GO 1722 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 3178 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human 148 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human GO 100 Genes GS194964: GO:0016202 regulation of striated muscle tissue development
Expand Tier I Human GO 4201 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 103 Genes GS206905: GO:0001657 ureteric bud development
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human GO 113 Genes GS197510: GO:0042471 ear morphogenesis
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 10 Genes GS203748: GO:0001840 neural plate development
Expand Tier I Human GO 15 Genes GS195930: GO:0048853 forebrain morphogenesis
Expand Tier I Human GO 3098 Genes GS203058: GO:0048519 negative regulation of biological process
Expand Tier I Human GO 4292 Genes GS204746: GO:0080090 regulation of primary metabolic process
Expand Tier I Human GO 82 Genes GS197825: GO:0001704 formation of primary germ layer
Expand Tier I Human CTD 6 Genes GS125167: Busulfan interacting genes (MeSH:D002066) in CTD
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 154 Genes GS198017: GO:0044344 cellular response to fibroblast growth factor stimulus
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 12 Genes GS198953: GO:0003148 outflow tract septum morphogenesis
Expand Tier I Human GO 39 Genes GS202028: GO:0055024 regulation of cardiac muscle tissue development
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Human 1715 Genes GS219769: http://www.broadinstitute.org/gsea/msigdb/cards/SIGNAL_TRANSDUCTION
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 537 Genes GS208127: GO:0000279 M phase
Expand Tier I Human GO 68 Genes GS197514: GO:0042475 odontogenesis of dentin-containing tooth
Expand Tier I Human GO 473 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human GO 4 Genes GS210015: GO:0060563 neuroepithelial cell differentiation
Expand Tier I Human GO 43 Genes GS199617: GO:0060425 lung morphogenesis
Expand Tier I Human GO 525 Genes GS208562: GO:0040008 regulation of growth
Expand Tier I Human GO 135 Genes GS209775: GO:0021915 neural tube development
Expand Tier I Human GO 156 Genes GS196324: GO:0048839 inner ear development
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 753 Genes GS204107: GO:0072359 circulatory system development
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 277 Genes GS193992: GO:0048732 gland development
Expand Tier I Human GO 238 Genes GS210016: GO:0060562 epithelial tube morphogenesis
Expand Tier I Human CTD 141 Genes GS123759: Testosterone interacting genes (MeSH:D013739) in CTD
Expand Tier I Human GO 4575 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 28 Genes GS172919: HP:0004408 Abnormality of the sense of smell
Expand Tier I Human GO 304 Genes GS206182: GO:0060537 muscle tissue development
Expand Human 1472 Genes GS219689: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human 72 Genes GS175158: HP:0011747 Abnormality of the anterior pituitary
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human GO 4065 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human 116 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier I Human GO 271 Genes GS202998: GO:0061458 reproductive system development
Expand Tier I Human GO 1169 Genes GS199781: GO:0043067 regulation of programmed cell death
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 129 Genes GS174925: HP:0000769 Abnormality of the breast
Expand Tier I Human GO 16 Genes GS194323: GO:0003203 endocardial cushion morphogenesis
Expand Tier I Human GO 32 Genes GS198586: GO:0021532 neural tube patterning
Expand Human 1472 Genes GS219906: http://www.broadinstitute.org/gsea/msigdb/cards/NUCLEUS
Expand Tier I Human GO 375 Genes GS207935: GO:0007507 heart development
Expand Tier I Human GO 476 Genes GS205089: GO:0033043 regulation of organelle organization
Expand Tier I Human GO 64 Genes GS206907: GO:0001658 branching involved in ureteric bud morphogenesis
Expand Tier I Human GO 107 Genes GS200150: GO:0022612 gland morphogenesis
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 1123 Genes GS210560: GO:0071310 cellular response to organic substance
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 1810 Genes GS198274: GO:0035556 intracellular signal transduction
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 34 Genes GS174723: HP:0000771 Gynecomastia
Expand Tier I Human GO 292 Genes GS194519: GO:0014706 striated muscle tissue development
Expand Tier I Human GO 63 Genes GS207813: GO:0048332 mesoderm morphogenesis
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human GO 82 Genes GS202417: GO:0007368 determination of left/right symmetry
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human GO 617 Genes GS209240: GO:0007169 transmembrane receptor protein tyrosine kinase signaling pathway
Expand Tier I Human GO 3468 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 1000 Genes GS199986: GO:0009719 response to endogenous stimulus
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human CTD 765 Genes GS124457: Mustard Gas interacting genes (MeSH:D009151) in CTD
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 40 Genes GS205301: GO:0045168 cell-cell signaling involved in cell fate commitment
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human GO 127 Genes GS206630: GO:0046661 male sex differentiation
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human GO 230 Genes GS209107: GO:0045137 development of primary sexual characteristics
Expand Tier I Human GO 364 Genes GS200690: GO:0002009 morphogenesis of an epithelium
Expand Tier I Human GO 492 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Human GO 45 Genes GS194496: GO:0001947 heart looping
Expand Tier I Human GO 1055 Genes GS208674: GO:0022402 cell cycle process
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human GO 24 Genes GS195491: GO:0030539 male genitalia development
Expand Tier I Human GO 18 Genes GS200230: GO:0005104 fibroblast growth factor receptor binding
Expand Tier I Human GO 84 Genes GS206901: GO:0001656 metanephros development
Expand Tier I Human GO 129 Genes GS193987: GO:0048738 cardiac muscle tissue development
Expand Tier I Human CTD 1759 Genes GS123048: Tretinoin interacting genes (MeSH:D014212) in CTD
Expand Tier I Human GO 3 Genes GS202027: GO:0055026 negative regulation of cardiac muscle tissue development
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 135 Genes GS202418: GO:0007369 gastrulation
Expand Tier I Human GO 2857 Genes GS195291: GO:0006355 regulation of transcription, DNA-dependent
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 105 Genes GS201782: GO:0021543 pallium development
Expand Tier I Human GO 1202 Genes GS195176: GO:0005102 receptor binding
Expand Tier I Human GO 3325 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human GO 140 Genes GS199001: GO:0060173 limb development
Expand Tier I Human GO 18 Genes GS200918: GO:0023019 signal transduction involved in regulation of gene expression
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 7650 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human CTD 1556 Genes GS125506: Valproic Acid interacting genes (MeSH:D014635) in CTD
Expand Tier I Human 26 Genes GS176003: HP:0100651 Type I diabetes mellitus
Expand Tier I Human GO 3402 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human GO 108 Genes GS205567: GO:0045787 positive regulation of cell cycle
Expand Tier I Human GO 110 Genes GS203402: GO:0007498 mesoderm development
Expand Tier I Human GO 30 Genes GS204886: GO:0010631 epithelial cell migration
Expand Tier I Human GO 904 Genes GS196918: GO:0048870 cell motility
Expand Tier I Human GO 90 Genes GS201858: GO:0009855 determination of bilateral symmetry
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human GO 1454 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 11 Genes GS201294: GO:0042487 regulation of odontogenesis of dentin-containing tooth
Expand Tier I Human GO 398 Genes GS202556: GO:0043434 response to peptide hormone stimulus
Expand Tier I Human GO 731 Genes GS194703: GO:0051726 regulation of cell cycle
Expand Tier I Human GO 1435 Genes GS205623: GO:0009888 tissue development
Expand Tier I Human GO 21 Genes GS196230: GO:0001823 mesonephros development
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 15 Genes GS200913: GO:0060037 pharyngeal system development
Expand Tier I Human 100 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 411 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 97 Genes GS194322: GO:0003206 cardiac chamber morphogenesis
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 514 Genes GS207807: GO:0043009 chordate embryonic development