Gene Details



POLR3A and homologs in 1 species are found in 167 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 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 1718 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human 24 Genes GS176754: HP:0002319 Thin corpus callosum
Expand Tier I Human GO 3714 Genes GS194038: GO:1901362 organic cyclic compound biosynthetic process
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human GO 2310 Genes GS195643: GO:0003677 DNA binding
Expand Tier I Human GO 1775 Genes GS194586: GO:0002376 immune system process
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 489 Genes GS197667: GO:0051240 positive regulation of multicellular organismal process
Expand Tier I Human GO 5120 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human GO 415 Genes GS200015: GO:0001816 cytokine production
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 100 Genes GS194658: GO:0000428 DNA-directed RNA polymerase complex
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 42 Genes GS197153: GO:0034062 RNA polymerase activity
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human GO 576 Genes GS203491: GO:0051707 response to other organism
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 34 Genes GS205984: GO:0032481 positive regulation of type I interferon production
Expand Tier I Human GO 373 Genes GS200016: GO:0001817 regulation of cytokine production
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 14 Genes GS176292: HP:0002127 Upper motor neuron abnormality
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8094 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human 214 Genes GS176167: HP:0001257 Spasticity
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 2921 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human GO 1832 Genes GS205511: GO:0001882 nucleoside binding
Expand Tier I Human GO 7 Genes GS198992: GO:0005666 DNA-directed RNA polymerase III complex
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 11 Genes GS176910: HP:0002174 Postural tremor
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 52 Genes GS202136: GO:0006383 transcription from RNA polymerase III promoter
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 95 Genes GS171217: HP:0003487 Babinski sign
Expand Tier I Human 196 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 245 Genes GS176806: HP:0003812 Phenotypic variability
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 18 Genes GS202133: GO:0006386 termination of RNA polymerase III transcription
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human GO 2711 Genes GS199273: GO:0043233 organelle lumen
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 GO 260 Genes GS204130: GO:0009615 response to virus
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 109 Genes GS204192: GO:0006354 DNA-dependent transcription, elongation
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 1822 Genes GS197443: GO:0032549 ribonucleoside binding
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 1476 Genes GS203369: GO:0005654 nucleoplasm
Expand Tier I Human 87 Genes GS176588: HP:0001272 Cerebellar atrophy
Expand Tier I Human GO 1091 Genes GS206909: GO:0006952 defense response
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human GO 461 Genes GS201730: GO:0002252 immune effector process
Expand Tier I Human GO 5190 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human GO 2665 Genes GS205543: GO:0070013 intracellular organelle lumen
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 8578 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 606 Genes GS208107: GO:0009607 response to biotic stimulus
Expand Tier I Human GO 101 Genes GS206003: GO:0030880 RNA polymerase complex
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 1043 Genes GS209480: GO:0006955 immune response
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human 413 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 3178 Genes GS204204: GO:0006351 transcription, DNA-dependent
Expand Tier I Human GO 196 Genes GS200021: GO:0001819 positive regulation of cytokine production
Expand Tier I Human GO 116 Genes GS204916: GO:0016779 nucleotidyltransferase activity
Expand Tier I Human GO 2603 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human GO 81 Genes GS198363: GO:0006353 DNA-dependent transcription, termination
Expand Tier I Human GO 885 Genes GS204919: GO:0016772 transferase activity, transferring phosphorus-containing groups
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 315 Genes GS170825: HP:0002167 Neurological speech impairment
Expand Tier I Human GO 3271 Genes GS199267: GO:0043234 protein complex
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 4138 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 3603 Genes GS198456: GO:0019438 aromatic compound biosynthetic process
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 259 Genes GS176172: HP:0001251 Ataxia
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 6 Genes GS172472: HP:0003429 Hypomyelination
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding
Expand Tier I Human 413 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human CTD 1291 Genes GS125402: Diethylnitrosamine interacting genes (MeSH:D004052) in CTD
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 29 Genes GS206821: GO:0032648 regulation of interferon-beta production
Expand Tier I Human 160 Genes GS176803: HP:0001260 Dysarthria
Expand Tier I Human GO 2092 Genes GS209551: GO:0031981 nuclear lumen
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human GO 3264 Genes GS205266: GO:0032774 RNA biosynthetic process
Expand Tier I Human GO 2756 Genes GS194555: GO:0031974 membrane-enclosed lumen
Expand Tier I Human GO 100 Genes GS202026: GO:0055029 nuclear DNA-directed RNA polymerase complex
Expand Tier I Human GO 31 Genes GS206292: GO:0032608 interferon-beta production
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human GO 20 Genes GS208874: GO:0032728 positive regulation of interferon-beta production
Expand Tier I Human GO 42 Genes GS198119: GO:0003899 DNA-directed RNA polymerase activity
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 214 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 818 Genes GS197472: GO:0044451 nucleoplasm part
Expand Tier I Human GO 5014 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 84 Genes GS170815: HP:0011400 Abnormal CNS myelination
Expand Tier I Human GO 1974 Genes GS203688: GO:0008270 zinc ion binding
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human GO 71 Genes GS206300: GO:0032606 type I interferon production
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human GO 3550 Genes GS203607: GO:0034654 nucleobase-containing compound biosynthetic process
Expand Tier I Human GO 3617 Genes GS206953: GO:0018130 heterocycle biosynthetic process
Expand Tier I Human 25 Genes GS177054: HP:0200010 Abnormal thickness of corpus callosum
Expand Tier I Human GO 3432 Genes GS203057: GO:0048518 positive regulation of biological process
Expand Tier I Human GO 2216 Genes GS209291: GO:0046914 transition metal ion binding
Expand Tier I Human GO 1362 Genes GS203494: GO:0051704 multi-organism process
Expand Tier I Human GO 3697 Genes GS194499: GO:0044271 cellular nitrogen compound biosynthetic process
Expand Tier I Human 413 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human GO 66 Genes GS194660: GO:0032479 regulation of type I interferon production
Expand Tier I Human GO 18 Genes GS202134: GO:0006385 transcription elongation from RNA polymerase III promoter
Expand Tier I Human 122 Genes GS173242: HP:0001337 Tremor
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 CTD 671 Genes GS121369: Clofibric Acid interacting genes (MeSH:D002995) in CTD
Expand Tier I Human 27 Genes GS175179: HP:0001310 Dysmetria
Expand Tier I Human GO 4245 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 31 Genes GS173142: HP:0002415 Leukodystrophy
Expand Tier I Human GO 1766 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 5280 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 528 Genes GS208131: GO:0045087 innate immune response
Expand Tier I Human GO 182 Genes GS209993: GO:0051607 defense response to virus
Expand Tier I Human 178 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 317 Genes GS176591: HP:0001276 Hypertonia
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle