Gene Details



TSC1 and homologs in 1 species are found in 645 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 GO 214 Genes GS203177: GO:0033124 regulation of GTP catabolic process
Expand Tier I Human GO 190 Genes GS200470: GO:0005938 cell cortex
Expand Tier I Human 10 Genes GS170952: HP:0009592 Astrocytoma
Expand Tier I Human 13 Genes GS173504: HP:0200036 Skin nodule
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 64 Genes GS174310: HP:0100705 Abnormality of the glial cells
Expand Tier I Human GO 1684 Genes GS204629: GO:1901564 organonitrogen compound metabolic process
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 250 Genes GS205884: GO:0016311 dephosphorylation
Expand Tier I Human GO 5216 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 2 Genes GS170987: HP:0010762 Chordoma
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
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 174 Genes GS172015: HP:0000969 Edema
Expand Tier I Human 109 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Human GO 790 Genes GS208912: GO:0046700 heterocycle catabolic process
Expand Tier I Human 154 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human GO 449 Genes GS197054: GO:0006195 purine nucleotide catabolic process
Expand Tier I Human GO 26 Genes GS194722: GO:0051893 regulation of focal adhesion assembly
Expand Tier I Human GO 1336 Genes GS200555: GO:0010605 negative regulation of macromolecule metabolic process
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
Expand Tier I Human GO 44 Genes GS201585: GO:0032231 regulation of actin filament bundle assembly
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 133 Genes GS197707: GO:0016331 morphogenesis of embryonic epithelium
Expand Tier I Human GO 649 Genes GS198498: GO:0050801 ion homeostasis
Expand Tier I Human GO 213 Genes GS195934: GO:0007015 actin filament organization
Expand Tier I Human GO 2507 Genes GS196934: GO:0065008 regulation of biological quality
Expand Tier I Human 138 Genes GS174644: HP:0000953 Hyperpigmentation of the skin
Expand Tier I Human GO 910 Genes GS202930: GO:2000113 negative regulation of cellular macromolecule biosynthetic process
Expand Tier I Human GO 722 Genes GS204317: GO:0009725 response to hormone stimulus
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 70 Genes GS203749: GO:0001843 neural tube closure
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 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 75 Genes GS209118: GO:0008361 regulation of cell size
Expand Tier I Human GO 362 Genes GS207065: GO:0051056 regulation of small GTPase mediated signal transduction
Expand Tier I Human 24 Genes GS173354: HP:0000230 Gingivitis
Expand Tier I Human 16 Genes GS174280: HP:0010566 Hamartoma
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 Human 117 Genes GS222319: Genes associated with high risk for Autism spectrum disorder with or without intellectual disability.
Expand Tier I Human GO 129 Genes GS206484: GO:0050658 RNA transport
Expand Tier I Human 3 Genes GS171170: HP:0100746 Macrodactyly of finger
Expand Tier I Human GO 1668 Genes GS202188: GO:0044248 cellular catabolic process
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 43 Genes GS173159: HP:0002239 Gastrointestinal hemorrhage
Expand Tier I Human 88 Genes GS176142: HP:0001034 Hypermelanotic macule
Expand Tier I Human GO 954 Genes GS195976: GO:0007155 cell adhesion
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 837 Genes GS196920: GO:0048878 chemical homeostasis
Expand Tier I Human GO 713 Genes GS204630: GO:1901565 organonitrogen compound catabolic process
Expand Tier I Human 4 Genes GS171007: HP:0011097 Epileptic spasms
Expand Tier I Human GO 654 Genes GS205165: GO:0010243 response to organic nitrogen
Expand Tier I Human GO 371 Genes GS200483: GO:0010608 posttranscriptional regulation of gene expression
Expand Tier I Human 5 Genes GS172860: HP:0004309 Ventricular preexcitation
Expand Tier I Human GO 444 Genes GS200490: GO:0061061 muscle structure development
Expand Tier I Human GO 553 Genes GS201022: GO:0071705 nitrogen compound transport
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 44 Genes GS171083: HP:0001328 Specific learning disability
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
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 739 Genes GS173290: HP:0011354 Generalized abnormality of 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 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human CTD 2047 Genes GS127205: Tamoxifen interacting genes (MeSH:D013629) in CTD
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human GO 401 Genes GS209401: GO:0046130 purine ribonucleoside catabolic process
Expand Tier I Human CTD 273 Genes GS122952: Arbutin interacting genes (MeSH:D001104) in CTD
Expand Tier I Human GO 401 Genes GS198972: GO:0006152 purine nucleoside catabolic process
Expand Tier I Human GO 4811 Genes GS204612: GO:0019222 regulation of metabolic process
Expand Tier I Human 5 Genes GS171757: HP:0001716 Wolff-Parkinson-White syndrome
Expand Tier I Human 117 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human CTD 709 Genes GS126466: Quercetin interacting genes (MeSH:D011794) in CTD
Expand Tier I Human GO 392 Genes GS196894: GO:0009207 purine ribonucleoside triphosphate catabolic process
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 275 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human CTD 218 Genes GS121147: Azacitidine interacting genes (MeSH:D001374) in CTD
Expand Tier I Human GO 98 Genes GS204614: GO:0019228 regulation of action potential in neuron
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human GO 9 Genes GS203874: GO:0032794 GTPase activating protein binding
Expand Tier I Human GO 4371 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 5 Genes GS176737: HP:0001482 Subcutaneous nodules
Expand Tier I Human GO 406 Genes GS207287: GO:0032870 cellular response to hormone stimulus
Expand Tier I Human GO 325 Genes GS199417: GO:1901069 guanosine-containing compound catabolic process
Expand Tier I Human GO 287 Genes GS202974: GO:0071375 cellular response to peptide hormone stimulus
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Human GO 129 Genes GS206491: GO:0050657 nucleic acid transport
Expand Tier I Human GO 83 Genes GS199765: GO:0047485 protein N-terminus binding
Expand Tier I Human GO 67 Genes GS206601: GO:0050821 protein stabilization
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 93 Genes GS174098: HP:0011792 Neoplasm by histology
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 412 Genes GS205333: GO:0032269 negative regulation of cellular protein metabolic process
Expand Tier I Human 20 Genes GS175686: HP:0002103 Abnormality of the pleura
Expand Tier I Human GO 748 Genes GS203608: GO:0034655 nucleobase-containing compound catabolic process
Expand Tier I Human 51 Genes GS172933: HP:0003745 Sporadic
Expand Tier I Human GO 111 Genes GS209705: GO:0035303 regulation of dephosphorylation
Expand Tier I Human GO 298 Genes GS199757: GO:0035239 tube morphogenesis
Expand Tier I Human 1 Genes GS173923: HP:0007042 Focal white matter lesions
Expand Tier I Human GO 781 Genes GS206190: GO:0048585 negative regulation of response to stimulus
Expand Tier I Human GO 149 Genes GS198845: GO:0007160 cell-matrix adhesion
Expand Tier I Human GO 43 Genes GS206661: GO:0048041 focal adhesion assembly
Expand Tier I Human GO 89 Genes GS205127: GO:0035051 cardiac cell differentiation
Expand Tier I Human 397 Genes GS171067: HP:0002664 Neoplasm
Expand Tier I Human 7 Genes GS175567: HP:0002888 Ependymoma
Expand Tier I Human GO 255 Genes GS196035: GO:0031252 cell leading edge
Expand Tier I Human 187 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human GO 1776 Genes GS205147: GO:0009966 regulation of signal transduction
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
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 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human 3 Genes GS174199: HP:0009721 Shagreen patch
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human GO 290 Genes GS206898: GO:0001655 urogenital system development
Expand Tier I Human GO 139 Genes GS204645: GO:0043547 positive regulation of GTPase activity
Expand Tier I Human GO 399 Genes GS206726: GO:0009261 ribonucleotide catabolic process
Expand Tier I Human 3 Genes GS174195: HP:0009729 Cardiac rhabdomyoma
Expand Tier I Human GO 821 Genes GS194041: GO:1901361 organic cyclic compound catabolic process
Expand Tier I Human GO 801 Genes GS206428: GO:0001932 regulation of protein phosphorylation
Expand Tier I Human GO 238 Genes GS206785: GO:0009118 regulation of nucleoside metabolic process
Expand Tier I Human 2 Genes GS174201: HP:0009727 Achromatic retinal patches
Expand Tier I Human 2 Genes GS174828: HP:0009716 Subependymal nodules
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 741 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human GO 459 Genes GS197665: GO:0051248 negative regulation of protein metabolic process
Expand Tier I Human GO 336 Genes GS203266: GO:0006140 regulation of nucleotide metabolic process
Expand Tier I Human 12 Genes GS172342: HP:0010615 Angiofibromas
Expand Tier I Human GO 457 Genes GS200656: GO:0060589 nucleoside-triphosphatase regulator activity
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 15 Genes GS171025: HP:0011146 Dialeptic seizures
Expand Tier I Human GO 54 Genes GS210270: GO:0021766 hippocampus development
Expand Tier I Human 117 Genes GS170989: HP:0010766 Ectopic calcification
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 1825 Genes GS205820: GO:0033036 macromolecule localization
Expand Tier I Human 7 Genes GS174942: HP:0100764 Lymphangioma
Expand Tier I Human 15 Genes GS175448: HP:0007359 Focal seizures
Expand Tier I Human GO 792 Genes GS201002: GO:0044270 cellular nitrogen compound catabolic process
Expand Tier I Human GO 678 Genes GS206354: GO:0023057 negative regulation of signaling
Expand Tier I Human GO 1004 Genes GS198240: GO:0031399 regulation of protein modification process
Expand Tier I Human GO 229 Genes GS200149: GO:0022613 ribonucleoprotein complex biogenesis
Expand Tier I Human GO 193 Genes GS206276: GO:0032970 regulation of actin filament-based process
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human GO 1324 Genes GS207282: GO:0031324 negative regulation of cellular metabolic process
Expand Tier I Human 72 Genes GS175809: HP:0011029 Internal hemorrhage
Expand Tier I Human GO 1540 Genes GS208664: GO:0008283 cell proliferation
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 10 Genes GS174312: HP:0100707 Abnormality of the astrocytes
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Human GO 1213 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human GO 772 Genes GS196593: GO:0006461 protein complex assembly
Expand Tier I Human GO 597 Genes GS199620: GO:0060429 epithelium development
Expand Tier I Human 197 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 399 Genes GS203082: GO:0009143 nucleoside triphosphate catabolic process
Expand Tier I Human 22 Genes GS175941: HP:0100835 Benign neoplasm of the central nervous system
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 151 Genes GS207521: GO:0042254 ribosome biogenesis
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 16 Genes GS174194: HP:0009728 Neoplasm of striated muscle
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 3 Genes GS174692: HP:0100898 Connective tissue nevi
Expand Tier I Human 5 Genes GS171419: HP:0004099 Macrodactyly
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human 5 Genes GS173189: HP:0000169 Gingival fibromatosis
Expand Tier I Human GO 2108 Genes GS209928: GO:0006996 organelle organization
Expand Tier I Human 10 Genes GS174620: HP:0007461 Hemangiomatosis
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human GO 59 Genes GS201944: GO:0007044 cell-substrate junction assembly
Expand Tier I Human GO 25 Genes GS194871: GO:0032856 activation of Ras GTPase activity
Expand Tier I Human GO 53 Genes GS196395: GO:0010811 positive regulation of cell-substrate adhesion
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 1751 Genes GS210579: GO:0051649 establishment of localization in cell
Expand Tier I Human 680 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human GO 129 Genes GS194457: GO:0051236 establishment of RNA localization
Expand Tier I Human GO 215 Genes GS200028: GO:0032869 cellular response to insulin stimulus
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 76 Genes GS206518: GO:0051017 actin filament bundle assembly
Expand Tier I Human GO 751 Genes GS202715: GO:0035637 multicellular organismal signaling
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human GO 165 Genes GS198581: GO:0021537 telencephalon development
Expand Tier I Human 4 Genes GS175092: HP:0008696 Renal hamartoma
Expand Tier I Human 212 Genes GS174189: HP:0001597 Abnormality of the nail
Expand Tier I Human GO 466 Genes GS204511: GO:0048729 tissue morphogenesis
Expand Tier I Human 67 Genes GS171115: HP:0001053 Hypopigmented skin patches
Expand Tier I Human 2 Genes GS174827: HP:0009717 Cortical tubers
Expand Tier I Human GO 273 Genes GS201756: GO:0042692 muscle cell differentiation
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human GO 1544 Genes GS202468: GO:0070887 cellular response to chemical stimulus
Expand Tier I Human 6 Genes GS176570: HP:0100803 Abnormality of the periungual region
Expand Tier I Human GO 333 Genes GS200182: GO:1900542 regulation of purine nucleotide metabolic process
Expand Tier I Human GO 1205 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human GO 3118 Genes GS206544: GO:2000112 regulation of cellular macromolecule biosynthetic process
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human GO 855 Genes GS209614: GO:0055086 nucleobase-containing small molecule metabolic process
Expand Tier I Human 57 Genes GS174179: HP:0002514 Cerebral calcification
Expand Tier I Human GO 1087 Genes GS203482: GO:0044093 positive regulation of molecular function
Expand Tier I Human GO 2511 Genes GS207903: GO:0044281 small molecule metabolic process
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 32 Genes GS176375: HP:0000269 Prominent occiput
Expand Tier I Human 123 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human GO 154 Genes GS208018: GO:0032318 regulation of Ras GTPase activity
Expand Tier I Human GO 439 Genes GS208021: GO:0051345 positive regulation of hydrolase activity
Expand Tier I Human 3 Genes GS171803: HP:0009554 Projection of scalp hair onto lateral cheek
Expand Tier I Human GO 754 Genes GS204108: GO:0072358 cardiovascular system development
Expand Tier I Human GO 458 Genes GS207995: GO:0009199 ribonucleoside triphosphate metabolic process
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 123 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human GO 2833 Genes GS198684: GO:0048523 negative regulation of cellular process
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 517 Genes GS208810: GO:0009259 ribonucleotide metabolic process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human GO 2050 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 446 Genes GS205566: GO:0045786 negative regulation of cell cycle
Expand Tier I Human 3 Genes GS174422: HP:0009730 Rhabdomyoma
Expand Tier I Human 15 Genes GS175473: HP:0200034 Skin papules
Expand Tier I Human 83 Genes GS171602: HP:0001965 Abnormality of the scalp
Expand Tier I Human GO 248 Genes GS194078: GO:0042391 regulation of membrane potential
Expand Tier I Human GO 503 Genes GS207389: GO:0009150 purine ribonucleotide metabolic process
Expand Tier I Human GO 432 Genes GS210177: GO:0031329 regulation of cellular catabolic process
Expand Tier I Human 40 Genes GS172679: HP:0001028 Hemangioma
Expand Tier I Human GO 244 Genes GS195111: GO:0071843 cellular component biogenesis at cellular level
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 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 279 Genes GS195069: GO:0030900 forebrain development
Expand Tier I Human 74 Genes GS175265: HP:0002733 Abnormality of the lymph nodes
Expand Tier I Human GO 332 Genes GS199111: GO:0044087 regulation of cellular component biogenesis
Expand Tier I Human GO 1815 Genes GS208187: GO:0010033 response to organic substance
Expand Tier I Human 232 Genes GS170999: HP:0000082 Abnormality of renal physiology
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human GO 71 Genes GS204189: GO:0021987 cerebral cortex development
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human GO 93 Genes GS202123: GO:0030426 growth cone
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 95 Genes GS202122: GO:0030427 site of polarized growth
Expand Tier I Human GO 4151 Genes GS206329: GO:0060255 regulation of macromolecule metabolic process
Expand Tier I Human GO 71 Genes GS204410: GO:0060606 tube closure
Expand Tier I Human GO 433 Genes GS207210: GO:0035295 tube development
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human GO 88 Genes GS202331: GO:0032319 regulation of Rho GTPase activity
Expand Tier I Human GO 994 Genes GS196927: GO:0065003 macromolecular complex assembly
Expand Tier I Human GO 324 Genes GS202057: GO:0006184 GTP catabolic process
Expand Tier I Human GO 561 Genes GS194647: GO:0071495 cellular response to endogenous stimulus
Expand Tier I Human 39 Genes GS174048: HP:0000729 Autism spectrum disorder
Expand Tier I Human 18 Genes GS175558: HP:0002516 Increased intracranial pressure
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Human GO 101 Genes GS208316: GO:0010810 regulation of cell-substrate adhesion
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human 246 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 458 Genes GS203083: GO:0009144 purine nucleoside triphosphate metabolic process
Expand Tier I Human GO 520 Genes GS201126: GO:0009792 embryo development ending in birth or egg hatching
Expand Tier I Human GO 638 Genes GS205146: GO:0009968 negative regulation of signal transduction
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 715 Genes GS200565: GO:0019725 cellular homeostasis
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 1126 Genes GS195108: GO:0071844 cellular component assembly at cellular level
Expand Tier I Human GO 583 Genes GS206781: GO:0009116 nucleoside metabolic process
Expand Tier I Human 4 Genes GS174556: HP:0002384 Focal seizures with impairment of consciousness or awareness
Expand Tier I Human 10 Genes GS174952: HP:0100761 Visceral angiomatosis
Expand Tier I Human GO 65 Genes GS193857: GO:0055007 cardiac muscle cell differentiation
Expand Tier I Human 54 Genes GS176964: HP:0011217 Abnormal shape of the occiput
Expand Tier I Human GO 136 Genes GS198984: GO:0006403 RNA localization
Expand Tier I Human 106 Genes GS171336: HP:0001732 Abnormality of the pancreas
Expand Tier I Human 71 Genes GS171600: HP:0000168 Abnormality of the gingiva
Expand Tier I Human GO 15 Genes GS210262: GO:0032007 negative regulation of TOR signaling cascade
Expand Tier I Human GO 73 Genes GS210275: GO:0021761 limbic system development
Expand Tier I Human GO 108 Genes GS198765: GO:0001838 embryonic epithelial tube formation
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 12 Genes GS175139: HP:0100749 Chest pain
Expand Tier I Human GO 116 Genes GS194241: GO:0035148 tube formation
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 GO 195 Genes GS208290: GO:0034330 cell junction organization
Expand Tier I Human GO 1852 Genes GS209010: GO:1901575 organic substance catabolic process
Expand Tier I Human CTD 90 Genes GS126476: Sirolimus interacting genes (MeSH:D020123) in CTD
Expand Tier I Human 391 Genes GS175537: HP:0011277 Abnormality of the urinary system physiology
Expand Tier I Human 12 Genes GS174423: HP:0009733 Glioma
Expand Tier I Human GO 407 Genes GS200813: GO:0030036 actin cytoskeleton organization
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 157 Genes GS174877: HP:0001892 Abnormal bleeding
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 1379 Genes GS209190: GO:0007049 cell cycle
Expand Tier I Human 403 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 20 Genes GS173827: HP:0002916 Abnormality of chromosome segregation
Expand Tier I Human GO 467 Genes GS194302: GO:0009166 nucleotide catabolic process
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 95 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human GO 1685 Genes GS199112: GO:0044085 cellular component biogenesis
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human GO 501 Genes GS197801: GO:0007420 brain development
Expand Tier I Human 266 Genes GS175823: HP:0002093 Respiratory insufficiency
Expand Tier I Human GO 975 Genes GS201034: GO:0030234 enzyme regulator activity
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 89 Genes GS194928: GO:0032320 positive regulation of Ras GTPase activity
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 61 Genes GS200952: GO:0017148 negative regulation of translation
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 35 Genes GS176775: HP:0001004 Lymphedema
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 540 Genes GS206784: GO:0009119 ribonucleoside metabolic process
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human 5 Genes GS174421: HP:0009731 Cerebral hamartomata
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 653 Genes GS195566: GO:0051338 regulation of transferase activity
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 543 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 67 Genes GS175160: HP:0002538 Abnormality of the cerebral cortex
Expand Tier I Human 61 Genes GS174375: HP:0002027 Abdominal pain
Expand Tier I Human GO 217 Genes GS195701: GO:0031589 cell-substrate adhesion
Expand Tier I Human GO 38 Genes GS198091: GO:0051492 regulation of stress fiber assembly
Expand Tier I Human GO 263 Genes GS200194: GO:0051493 regulation of cytoskeleton organization
Expand Tier I Human GO 187 Genes GS210003: GO:0044445 cytosolic part
Expand Tier I Human 11 Genes GS176796: HP:0001269 Hemiparesis
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 36 Genes GS171175: HP:0001541 Ascites
Expand Tier I Human GO 89 Genes GS203747: GO:0001841 neural tube formation
Expand Tier I Human GO 1204 Genes GS204610: GO:0019220 regulation of phosphate metabolic process
Expand Tier I Human GO 83 Genes GS207579: GO:0007272 ensheathment of neurons
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 1160 Genes GS206657: GO:0043933 macromolecular complex subunit organization
Expand Tier I Human GO 1003 Genes GS201264: GO:0009890 negative regulation of biosynthetic process
Expand Tier I Human GO 5379 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human GO 1929 Genes GS201025: GO:0071702 organic substance transport
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 626 Genes GS174335: HP:0001871 Abnormality of blood and blood-forming tissues
Expand Tier I Human 2 Genes GS174202: HP:0009724 Subungual fibromas
Expand Tier I Human GO 1216 Genes GS199495: GO:0051174 regulation of phosphorus metabolic process
Expand Tier I Human GO 474 Genes GS200117: GO:0051130 positive regulation of cellular component organization
Expand Tier I Human GO 20 Genes GS207731: GO:0032862 activation of Rho GTPase activity
Expand Tier I Human GO 5601 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 2 Genes GS174196: HP:0009722 Dental enamel pits
Expand Tier I Human GO 136 Genes GS201741: GO:0001508 regulation of action potential
Expand Tier I Human 12 Genes GS171053: HP:0002105 Hemoptysis
Expand Tier I Human 360 Genes GS174099: HP:0011793 Neoplasm by anatomical site
Expand Tier I Human GO 135 Genes GS209775: GO:0021915 neural tube development
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 649 Genes GS207805: GO:0043005 neuron projection
Expand Tier I Human GO 930 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human GO 754 Genes GS204107: GO:0072359 circulatory system development
Expand Tier I Human GO 5558 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 121 Genes GS205124: GO:0030027 lamellipodium
Expand Tier I Human 213 Genes GS176040: HP:0011032 Abnormality of fluid regulation
Expand Tier I Human 2 Genes GS176157: HP:0100826 Neoplasm of the nail
Expand Tier I Human GO 238 Genes GS210016: GO:0060562 epithelial tube morphogenesis
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human 271 Genes GS174948: HP:0100763 Abnormality of the lymphatic system
Expand Tier I Human GO 586 Genes GS201310: GO:0006873 cellular ion homeostasis
Expand Tier I Human GO 1180 Genes GS195151: GO:0019637 organophosphate metabolic process
Expand Tier I Human 90 Genes GS171351: HP:0003581 Adult onset
Expand Tier I Human 43 Genes GS171179: HP:0003764 Nevus
Expand Tier I Human GO 304 Genes GS206182: GO:0060537 muscle tissue development
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 55 Genes GS174648: HP:0000957 Cafe-au-lait spot
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 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 Human GO 524 Genes GS199459: GO:0042278 purine nucleoside metabolic process
Expand Tier I Human GO 113 Genes GS203828: GO:0051168 nuclear export
Expand Tier I Human GO 632 Genes GS204649: GO:0043549 regulation of kinase activity
Expand Tier I Human 50 Genes GS174295: HP:0010786 Urinary tract neoplasm
Expand Tier I Human GO 1430 Genes GS201262: GO:0009892 negative regulation of metabolic process
Expand Tier I Human GO 523 Genes GS204496: GO:0019693 ribose phosphate metabolic process
Expand Tier I Human 913 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human GO 237 Genes GS203173: GO:0033121 regulation of purine nucleotide catabolic process
Expand Tier I Human 79 Genes GS172284: HP:0000821 Hypothyroidism
Expand Tier I Human GO 637 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human GO 238 Genes GS202895: GO:0030811 regulation of nucleotide catabolic process
Expand Tier I Human GO 170 Genes GS203936: GO:0034329 cell junction assembly
Expand Tier I Human GO 375 Genes GS207935: GO:0007507 heart development
Expand Tier I Human 123 Genes GS176258: HP:0004370 Abnormality of temperature regulation
Expand Tier I Human GO 477 Genes GS205089: GO:0033043 regulation of organelle organization
Expand Tier I Human 3 Genes GS174830: HP:0009719 Hypomelanotic macules
Expand Tier I Human GO 1993 Genes GS207862: GO:0009056 catabolic process
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 793 Genes GS198455: GO:0019439 aromatic compound catabolic process
Expand Tier I Human GO 1126 Genes GS210560: GO:0071310 cellular response to organic substance
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 1817 Genes GS198274: GO:0035556 intracellular signal transduction
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human GO 292 Genes GS194519: GO:0014706 striated muscle tissue development
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human GO 339 Genes GS203827: GO:0051169 nuclear transport
Expand Tier I Human GO 83 Genes GS209121: GO:0008366 axon ensheathment
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 709 Genes GS210435: GO:0072521 purine-containing compound metabolic process
Expand Tier I Human GO 2027 Genes GS206356: GO:0023051 regulation of signaling
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human GO 617 Genes GS209240: GO:0007169 transmembrane receptor protein tyrosine kinase signaling pathway
Expand Tier I Human GO 376 Genes GS197555: GO:0007050 cell cycle arrest
Expand Tier I Human GO 3487 Genes GS199499: GO:0051171 regulation of nitrogen compound metabolic process
Expand Tier I Human GO 453 Genes GS210437: GO:0072523 purine-containing compound catabolic 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 2 Genes GS208483: GO:0006407 rRNA export from nucleus
Expand Tier I Human GO 2545 Genes GS203335: GO:0048513 organ development
Expand Tier I Human GO 109 Genes GS207298: GO:0072175 epithelial tube formation
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human GO 519 Genes GS198012: GO:0046434 organophosphate catabolic process
Expand Tier I Human GO 163 Genes GS208926: GO:0035023 regulation of Rho protein signal transduction
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 67 Genes GS173092: HP:0004375 Neoplasm of the nervous system
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 475 Genes GS203080: GO:0009141 nucleoside triphosphate metabolic process
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 493 Genes GS201848: GO:0048598 embryonic morphogenesis
Expand Tier I Human GO 264 Genes GS207796: GO:0030155 regulation of cell adhesion
Expand Tier I Human 89 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human GO 445 Genes GS203202: GO:0030695 GTPase regulator activity
Expand Tier I Human GO 1056 Genes GS208674: GO:0022402 cell cycle process
Expand Tier I Human GO 268 Genes GS199739: GO:0046578 regulation of Ras protein signal transduction
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 5 Genes GS171278: HP:0100544 Neoplasm of the heart
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 122 Genes GS205569: GO:0045785 positive regulation of cell adhesion
Expand Tier I Human 162 Genes GS175556: HP:0011675 Arrhythmia
Expand Tier I Human GO 774 Genes GS208730: GO:0070271 protein complex biogenesis
Expand Tier I Human 26 Genes GS176856: HP:0005584 Renal cell carcinoma
Expand Tier I Human GO 129 Genes GS193987: GO:0048738 cardiac muscle tissue development
Expand Tier I Human GO 803 Genes GS206780: GO:0009117 nucleotide metabolic process
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 Tier I Human GO 58 Genes GS203857: GO:0051291 protein heterooligomerization
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 40 Genes GS171823: HP:0000113 Polycystic kidney dysplasia
Expand Tier I Human 52 Genes GS176460: HP:0000790 Hematuria
Expand Tier I Human GO 134 Genes GS198495: GO:0050808 synapse organization
Expand Tier I Human GO 835 Genes GS210330: GO:0006412 translation
Expand Tier I Human GO 2431 Genes GS209232: GO:0006796 phosphate-containing compound metabolic process
Expand Tier I Human GO 631 Genes GS209611: GO:0055082 cellular chemical homeostasis
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 5369 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 105 Genes GS201782: GO:0021543 pallium development
Expand Tier I Human GO 3344 Genes GS205369: GO:0010468 regulation of gene expression
Expand Tier I Human 14 Genes GS176517: HP:0007894 Hypopigmentation of the fundus
Expand Tier I Human GO 174 Genes GS197559: GO:0032956 regulation of actin cytoskeleton organization