Details for: TNRC6A

Gene ID: 27327

Gene Type:  Protein-coding  - A gene that serves as a template for producing a messenger RNA (mRNA) molecule, which is then translated into a functional protein.

Symbol: TNRC6A

Ensembl ID: ENSG00000090905

Description: trinucleotide repeat containing adaptor 6A

Selected Context(s):  Overall

Cell Significance Landscape

Contexts:

Associated with

Significant Cells

Cell Significance Index (CSI) scores for the chosen context(s)

  • VIP GABAergic cortical interneuron CL4023016
    CSI 78.11
    rCSI 93.31%
    PRS 12.2
  • pvalb GABAergic cortical interneuron CL4023018
    CSI 76.34
    rCSI 94.97%
    PRS 11.59
  • sst GABAergic cortical interneuron CL4023017
    CSI 71.39
    rCSI 92.03%
    PRS 13
  • choroid plexus epithelial cell CL0000706
    CSI 60.33
    rCSI 98.79%
    PRS 16.1
  • Bergmann glial cell CL0000644
    CSI 56.39
    rCSI 77.16%
    PRS 20.83
  • cardiac muscle cell CL0000746
    CSI 54.75
    rCSI 78.57%
    PRS 16.24
  • sncg GABAergic cortical interneuron CL4023015
    CSI 54.21
    rCSI 87.19%
    PRS 13.53
  • differentiation-committed oligodendrocyte precursor CL4023059
    CSI 52.44
    rCSI 95.28%
    PRS 17.9
  • cerebellar granule cell CL0001031
    CSI 52.42
    rCSI 77.07%
    PRS 19.39
  • lamp5 GABAergic cortical interneuron CL4023011
    CSI 51.07
    rCSI 85.73%
    PRS 12.41
  • adipocyte CL0000136
    CSI 51.07
    rCSI 65.57%
    PRS 20.37
  • astrocyte CL0000127
    CSI 49.07
    rCSI 100%
    PRS 13.45
  • ependymal cell CL0000065
    CSI 47.58
    rCSI 96.54%
    PRS 10.79
  • caudal ganglionic eminence derived cortical interneuron CL4023064
    CSI 47.29
    rCSI 83.52%
    PRS 12.32
  • inhibitory interneuron CL0000498
    CSI 42.87
    rCSI 98.96%
    PRS 16.94
  • L2/3 intratelencephalic projecting glutamatergic neuron CL4030059
    CSI 41.35
    rCSI 89.69%
    PRS 15.05
  • oligodendrocyte precursor cell CL0002453
    CSI 39.26
    rCSI 86.38%
    PRS 17.63
  • astrocyte of the cerebral cortex CL0002605
    CSI 38.44
    rCSI 86.19%
    PRS 12.97
  • L4 intratelencephalic projecting glutamatergic neuron CL4030063
    CSI 38.32
    rCSI 91.66%
    PRS 13.87
  • neuron CL0000540
    CSI 35.04
    rCSI 93.31%
    PRS 18.22
  • L2/3-6 intratelencephalic projecting glutamatergic neuron CL4023040
    CSI 34
    rCSI 82.64%
    PRS 12.17
  • IgG plasma cell CL0000985
    CSI 32.7
    rCSI 39.17%
    PRS 36.21
  • retinal ganglion cell CL0000740
    CSI 32.35
    rCSI 71.47%
    PRS 14.99
  • kidney loop of Henle thin descending limb epithelial cell CL1001111
    CSI 31.62
    rCSI 44.82%
    PRS 19.38
  • glycinergic amacrine cell CL4030028
    CSI 28.66
    rCSI 74.67%
    PRS 21.12
  • L6b glutamatergic cortical neuron CL4023038
    CSI 27.73
    rCSI 86.67%
    PRS 13.23
  • chandelier pvalb GABAergic cortical interneuron CL4023036
    CSI 27.51
    rCSI 86.04%
    PRS 14.25
  • L5/6 near-projecting glutamatergic neuron CL4030067
    CSI 27.46
    rCSI 90.23%
    PRS 13.67
  • neuroblast (sensu Vertebrata) CL0000031
    CSI 25.3
    rCSI 32.47%
    PRS 20.2
  • glioblast CL0000030
    CSI 24.49
    rCSI 39.07%
    PRS 17.92
  • retina horizontal cell CL0000745
    CSI 24.22
    rCSI 36.92%
    PRS 19.38
  • L5 extratelencephalic projecting glutamatergic cortical neuron CL4023041
    CSI 23.23
    rCSI 83.58%
    PRS 11.68
  • near-projecting glutamatergic cortical neuron CL4023012
    CSI 22.32
    rCSI 84.35%
    PRS 12.81
  • amacrine cell CL0000561
    CSI 22.14
    rCSI 64.15%
    PRS 16.11
  • neuroblast (sensu Nematoda and Protostomia) CL0000338
    CSI 22.07
    rCSI 25.49%
    PRS 18.29
  • radial glial cell CL0000681
    CSI 21.61
    rCSI 30.03%
    PRS 21.37
  • glutamatergic neuron CL0000679
    CSI 21.45
    rCSI 44.07%
    PRS 20.72
  • hepatic stellate cell CL0000632
    CSI 21.18
    rCSI 79.33%
    PRS 17.68
  • parietal epithelial cell CL1000452
    CSI 20.51
    rCSI 54.81%
    PRS 17.46
  • GABAergic amacrine cell CL4030027
    CSI 20.37
    rCSI 69.76%
    PRS 18.35
  • H1 horizontal cell CL0004217
    CSI 19.56
    rCSI 77.49%
    PRS 28.33
  • epithelial cell of proximal tubule CL0002306
    CSI 19.25
    rCSI 47.02%
    PRS 20.59
  • rod bipolar cell CL0000751
    CSI 19.15
    rCSI 34.41%
    PRS 17.33
  • interneuron CL0000099
    CSI 18.14
    rCSI 36.42%
    PRS 15.51
  • GABAergic neuron CL0000617
    CSI 18.12
    rCSI 60.71%
    PRS 15.03
  • vascular leptomeningeal cell CL4023051
    CSI 17.5
    rCSI 30.69%
    PRS 15.96
  • retinal bipolar neuron CL0000748
    CSI 17.32
    rCSI 32.45%
    PRS 15.06
  • H2 horizontal cell CL0004218
    CSI 16.89
    rCSI 84%
    PRS 22.8
  • macroglial cell CL0000126
    CSI 16.57
    rCSI 42.59%
    PRS 27.22
  • hepatocyte CL0000182
    CSI 15.81
    rCSI 28.29%
    PRS 19.4
  • keratocyte CL0002363
    CSI 15.05
    rCSI 36.17%
    PRS 30.79
  • kidney connecting tubule epithelial cell CL1000768
    CSI 14.7
    rCSI 37.29%
    PRS 15.88
  • corticothalamic-projecting glutamatergic cortical neuron CL4023013
    CSI 13.8
    rCSI 81.25%
    PRS 13.01
  • centrilobular region hepatocyte CL0019029
    CSI 13.67
    rCSI 35.68%
    PRS 31.96
  • chondrocyte CL0000138
    CSI 13.5
    rCSI 21.47%
    PRS 17.66
  • naive B cell CL0000788
    CSI 13.35
    rCSI 11.45%
    PRS 34.05
  • epicardial adipocyte CL1000309
    CSI 13.02
    rCSI 42.35%
    PRS 25.69
  • diffuse bipolar 3a cell CL4033029
    CSI 12.7
    rCSI 86.43%
    PRS 22.34
  • periportal region hepatocyte CL0019026
    CSI 12.62
    rCSI 49.07%
    PRS 28.6
  • pro-B cell CL0000826
    CSI 12.59
    rCSI 10.42%
    PRS 21.29
  • cerebral cortex endothelial cell CL1001602
    CSI 12.52
    rCSI 21.65%
    PRS 15.99
  • mucosal invariant T cell CL0000940
    CSI 12.51
    rCSI 10.1%
    PRS 32.57
  • invaginating midget bipolar cell CL4033034
    CSI 12.35
    rCSI 72.91%
    PRS 22.79
  • central nervous system neuron CL2000029
    CSI 11.79
    rCSI 86.66%
    PRS 12.52
  • diffuse bipolar 6 cell CL4033032
    CSI 11.72
    rCSI 61.65%
    PRS 25.08
  • mural cell CL0008034
    CSI 11.63
    rCSI 39.4%
    PRS 21.58
  • diffuse bipolar 3b cell CL4033030
    CSI 11.57
    rCSI 76.78%
    PRS 22.78
  • OFFx cell CL4033036
    CSI 11.57
    rCSI 54.41%
    PRS 23.11
  • CD4-positive, alpha-beta thymocyte CL0000810
    CSI 11.56
    rCSI 9.26%
    PRS 37.15
  • S cone cell CL0003050
    CSI 11.56
    rCSI 50.78%
    PRS 19.25
  • blood vessel endothelial cell CL0000071
    CSI 10.87
    rCSI 22.55%
    PRS 20.86
  • retinal cone cell CL0000573
    CSI 10.62
    rCSI 17.1%
    PRS 16.01
  • renal interstitial pericyte CL1001318
    CSI 10.46
    rCSI 28.84%
    PRS 19.56
  • medium spiny neuron CL1001474
    CSI 10.3
    rCSI 88.74%
    PRS 10.85
  • alveolar type 1 fibroblast cell CL4028004
    CSI 10.29
    rCSI 11.27%
    PRS 23.62
  • hematopoietic precursor cell CL0008001
    CSI 10.02
    rCSI 10.31%
    PRS 33.89
  • cholangiocyte CL1000488
    CSI 9.8
    rCSI 58.72%
    PRS 36.58
  • naive thymus-derived CD8-positive, alpha-beta T cell CL0000900
    CSI 9.71
    rCSI 6.82%
    PRS 47.93
  • neural crest cell CL0011012
    CSI 9.7
    rCSI 7.67%
    PRS 14.41
  • oligodendrocyte CL0000128
    CSI 9.62
    rCSI 28.43%
    PRS 19.97
  • endothelial cell of pericentral hepatic sinusoid CL0019022
    CSI 9.16
    rCSI 28.23%
    PRS 31.17
  • transit amplifying cell of colon CL0009011
    CSI 8.96
    rCSI 10.52%
    PRS 24.07
  • flat midget bipolar cell CL4033033
    CSI 8.85
    rCSI 63.27%
    PRS 22.17
  • regular atrial cardiac myocyte CL0002129
    CSI 8.71
    rCSI 28.03%
    PRS 21.85
  • neuroendocrine cell CL0000165
    CSI 8.47
    rCSI 32.74%
    PRS 40.67
  • diffuse bipolar 1 cell CL4033027
    CSI 8.34
    rCSI 62.7%
    PRS 22
  • cerebral cortex neuron CL0010012
    CSI 8.2
    rCSI 33.41%
    PRS 21.46
  • diffuse bipolar 2 cell CL4033028
    CSI 8
    rCSI 61.98%
    PRS 23.19
  • starburst amacrine cell CL0004232
    CSI 7.98
    rCSI 67.16%
    PRS 22.99
  • CD14-positive, CD16-positive monocyte CL0002397
    CSI 7.81
    rCSI 10.24%
    PRS 29.94
  • class switched memory B cell CL0000972
    CSI 7.79
    rCSI 5.82%
    PRS 35.11
  • epithelial cell of lower respiratory tract CL0002632
    CSI 7.76
    rCSI 6.02%
    PRS 20.1
  • regular ventricular cardiac myocyte CL0002131
    CSI 7.68
    rCSI 47.94%
    PRS 16.32
  • neural cell CL0002319
    CSI 7.51
    rCSI 28.34%
    PRS 27.35
  • serotonergic neuron CL0000850
    CSI 7.45
    rCSI 33.3%
    PRS 14.02
  • kidney loop of Henle thin ascending limb epithelial cell CL1001107
    CSI 7.38
    rCSI 19.08%
    PRS 19.48
  • precursor B cell CL0000817
    CSI 7.36
    rCSI 6.45%
    PRS 27.96
  • myeloid leukocyte CL0000766
    CSI 7.19
    rCSI 6.64%
    PRS 21.77
  • alveolar adventitial fibroblast CL4028006
    CSI 7.18
    rCSI 11.34%
    PRS 21.03
  • small intestine goblet cell CL1000495
    CSI 7.11
    rCSI 15.57%
    PRS 27.99
  • peripheral nervous system neuron CL2000032
    CSI -1.6
    rCSI -2.2%
    PRS 18.5%
  • paneth cell CL0000510
    CSI -1.3
    rCSI -1.9%
    PRS 32.6%
  • elicited macrophage CL0000861
    CSI -1.0
    rCSI -1.0%
    PRS 24.6%
  • mesenchymal cell CL0008019
    CSI -0.9
    rCSI -2.2%
    PRS 21.0%
  • enteroendocrine cell of colon CL0009042
    CSI -0.6
    rCSI -2.7%
    PRS 50.7%
  • T-helper 1 cell CL0000545
    CSI -0.2
    rCSI -0.4%
    PRS 49.9%
  • mesenchymal stem cell CL0000134
    CSI 0.2
    rCSI 1.6%
    PRS 36.9%
  • cytotoxic T cell CL0000910
    CSI 0.2
    rCSI 0.9%
    PRS 30.8%
  • pancreatic stellate cell CL0002410
    CSI 0.2
    rCSI 1.1%
    PRS 30.9%
  • corneal epithelial cell CL0000575
    CSI 0.2
    rCSI 0.6%
    PRS 36.6%
  • enteric neuron CL0007011
    CSI 0.3
    rCSI 3.7%
    PRS 48.2%
  • pluripotent stem cell CL0002248
    CSI 0.3
    rCSI 8.3%
    PRS 44.9%
  • paneth cell of colon CL0009009
    CSI 0.4
    rCSI 3.4%
    PRS 52.1%
  • P/D1 enteroendocrine cell CL0002268
    CSI 0.4
    rCSI 2.4%
    PRS 47.2%
  • type EC enteroendocrine cell CL0000577
    CSI 0.5
    rCSI 1.6%
    PRS 33.8%
  • enterocyte of epithelium of small intestine CL1000334
    CSI 0.5
    rCSI 7.2%
    PRS 49.2%
  • effector memory CD8-positive, alpha-beta T cell, terminally differentiated CL0001062
    CSI 0.5
    rCSI 2.4%
    PRS 27.7%
  • foveolar cell of stomach CL0002179
    CSI 0.6
    rCSI 1.2%
    PRS 33.1%
  • pancreatic ductal cell CL0002079
    CSI 0.6
    rCSI 1.1%
    PRS 21.5%
  • luminal cell of prostate epithelium CL0002340
    CSI 0.6
    rCSI 3.3%
    PRS 36.7%
  • pancreatic PP cell CL0002275
    CSI 0.7
    rCSI 2.6%
    PRS 35.6%
  • granulocyte monocyte progenitor cell CL0000557
    CSI 0.7
    rCSI 0.6%
    PRS 23.7%
  • mature alpha-beta T cell CL0000791
    CSI 0.7
    rCSI 2.5%
    PRS 35.9%
  • mucus secreting cell CL0000319
    CSI 0.8
    rCSI 1.3%
    PRS 26.9%
  • pancreatic epsilon cell CL0005019
    CSI 0.8
    rCSI 3.8%
    PRS 45.1%
  • smooth muscle cell of the pulmonary artery CL0002591
    CSI 0.8
    rCSI 6.2%
    PRS 53.4%
  • transit amplifying cell of small intestine CL0009012
    CSI 0.9
    rCSI 3.8%
    PRS 38.3%
  • deuterosomal cell CL4033044
    CSI 0.9
    rCSI 3.1%
    PRS 33.0%
  • erythroid lineage cell CL0000764
    CSI 0.9
    rCSI 6.0%
    PRS 44.5%
  • endothelial cell of venule CL1000414
    CSI 1.0
    rCSI 8.5%
    PRS 64.2%
  • Langerhans cell CL0000453
    CSI 1.0
    rCSI 1.5%
    PRS 36.5%
  • Hofbauer cell CL3000001
    CSI 1.0
    rCSI 1.9%
    PRS 26.5%
  • enteric smooth muscle cell CL0002504
    CSI 1.1
    rCSI 1.5%
    PRS 23.5%
  • CD1c-positive myeloid dendritic cell CL0002399
    CSI 1.1
    rCSI 1.3%
    PRS 25.2%
  • acinar cell CL0000622
    CSI 1.1
    rCSI 1.6%
    PRS 27.4%
  • innate lymphoid cell CL0001065
    CSI 1.1
    rCSI 2.3%
    PRS 31.1%
  • tuft cell of colon CL0009041
    CSI 1.1
    rCSI 2.6%
    PRS 41.0%
  • retinal pigment epithelial cell CL0002586
    CSI 1.2
    rCSI 2.3%
    PRS 22.0%
  • neuroplacodal cell CL0000032
    CSI 1.2
    rCSI 11.0%
    PRS 51.9%
  • colon goblet cell CL0009039
    CSI 1.2
    rCSI 2.8%
    PRS 31.1%
  • T-helper 17 cell CL0000899
    CSI 1.3
    rCSI 1.0%
    PRS 37.3%
  • mesenchymal stem cell of adipose tissue CL0002570
    CSI 1.4
    rCSI 7.6%
    PRS 50.9%
  • colon epithelial cell CL0011108
    CSI 1.5
    rCSI 1.5%
    PRS 19.6%
  • squamous epithelial cell CL0000076
    CSI 1.5
    rCSI 3.6%
    PRS 25.9%
  • microcirculation associated smooth muscle cell CL0008035
    CSI 1.5
    rCSI 4.4%
    PRS 23.6%
  • intestinal epithelial cell CL0002563
    CSI 1.6
    rCSI 1.6%
    PRS 21.8%
  • respiratory suprabasal cell CL4033048
    CSI 1.6
    rCSI 2.0%
    PRS 24.2%
  • pancreatic acinar cell CL0002064
    CSI 1.6
    rCSI 2.1%
    PRS 23.0%
  • placental villous trophoblast CL2000060
    CSI 1.6
    rCSI 2.4%
    PRS 19.6%
  • common dendritic progenitor CL0001029
    CSI 1.6
    rCSI 2.0%
    PRS 27.2%
  • megakaryocyte-erythroid progenitor cell CL0000050
    CSI 1.6
    rCSI 1.5%
    PRS 19.0%
  • mature B cell CL0000785
    CSI 1.6
    rCSI 1.4%
    PRS 26.3%
  • melanocyte CL0000148
    CSI 1.6
    rCSI 1.2%
    PRS 18.1%
  • pancreatic A cell CL0000171
    CSI 1.7
    rCSI 1.8%
    PRS 22.3%
  • common myeloid progenitor CL0000049
    CSI 1.7
    rCSI 1.4%
    PRS 21.1%
  • paneth cell of epithelium of small intestine CL1000343
    CSI 1.7
    rCSI 4.7%
    PRS 32.3%
  • extravillous trophoblast CL0008036
    CSI 1.7
    rCSI 2.1%
    PRS 18.4%
  • tendon cell CL0000388
    CSI 1.7
    rCSI 4.5%
    PRS 51.5%
  • myeloid dendritic cell CL0000782
    CSI 1.7
    rCSI 2.5%
    PRS 31.6%
  • adventitial cell CL0002503
    CSI 1.8
    rCSI 4.2%
    PRS 31.6%
  • central memory CD8-positive, alpha-beta T cell CL0000907
    CSI 1.8
    rCSI 1.2%
    PRS 25.8%
  • effector CD4-positive, alpha-beta T cell CL0001044
    CSI 1.8
    rCSI 5.1%
    PRS 31.3%
  • duct epithelial cell CL0000068
    CSI 1.8
    rCSI 2.6%
    PRS 22.2%
  • pancreatic D cell CL0000173
    CSI 1.8
    rCSI 1.8%
    PRS 22.6%
  • type L enteroendocrine cell CL0002279
    CSI 1.9
    rCSI 3.5%
    PRS 40.5%
  • basal-myoepithelial cell of mammary gland CL0002324
    CSI 1.9
    rCSI 3.6%
    PRS 43.8%
  • lung macrophage CL1001603
    CSI 1.9
    rCSI 4.3%
    PRS 24.4%
  • CD8-positive, alpha-beta cytotoxic T cell CL0000794
    CSI 1.9
    rCSI 2.3%
    PRS 36.3%
  • enteroglial cell CL4040002
    CSI 2.0
    rCSI 10.3%
    PRS 34.9%
  • lung ciliated cell CL1000271
    CSI 2.0
    rCSI 2.3%
    PRS 15.4%
  • intestinal crypt stem cell of colon CL0009043
    CSI 2.0
    rCSI 15.1%
    PRS 37.9%
  • tissue-resident macrophage CL0000864
    CSI 2.0
    rCSI 9.4%
    PRS 41.5%
  • intestinal tuft cell CL0019032
    CSI 2.1
    rCSI 3.1%
    PRS 23.9%
  • pulmonary alveolar type 1 cell CL0002062
    CSI 2.1
    rCSI 11.8%
    PRS 26.6%
  • ciliated columnar cell of tracheobronchial tree CL0002145
    CSI 2.1
    rCSI 4.7%
    PRS 21.6%
  • multi-ciliated epithelial cell CL0005012
    CSI 2.1
    rCSI 2.1%
    PRS 17.9%
  • eye photoreceptor cell CL0000287
    CSI 2.1
    rCSI 23.2%
    PRS 48.1%
  • helper T cell CL0000912
    CSI 2.2
    rCSI 3.0%
    PRS 29.0%
  • contractile cell CL0000183
    CSI 2.2
    rCSI 6.4%
    PRS 20.2%
  • cardiac blood vessel endothelial cell CL0010006
    CSI 2.2
    rCSI 15.4%
    PRS 23.7%
  • type B pancreatic cell CL0000169
    CSI 2.2
    rCSI 4.8%
    PRS 19.4%
  • intestinal crypt stem cell of small intestine CL0009017
    CSI 2.2
    rCSI 6.0%
    PRS 27.1%
  • myoepithelial cell CL0000185
    CSI 2.3
    rCSI 5.7%
    PRS 25.9%
  • fast muscle cell CL0000190
    CSI 2.3
    rCSI 9.0%
    PRS 43.2%
  • erythrocyte CL0000232
    CSI 2.3
    rCSI 5.2%
    PRS 27.9%
  • lymphoid lineage restricted progenitor cell CL0000838
    CSI 2.3
    rCSI 9.1%
    PRS 34.3%
  • tracheobronchial smooth muscle cell CL0019019
    CSI 2.4
    rCSI 4.2%
    PRS 27.3%
  • conjunctival epithelial cell CL1000432
    CSI 2.4
    rCSI 3.7%
    PRS 21.1%
  • common lymphoid progenitor CL0000051
    CSI 2.4
    rCSI 3.2%
    PRS 39.5%
  • brain vascular cell CL4023072
    CSI 2.4
    rCSI 25.0%
    PRS 24.6%
  • pulmonary artery endothelial cell CL1001568
    CSI 2.5
    rCSI 3.4%
    PRS 31.6%
  • OFF-bipolar cell CL0000750
    CSI 2.6
    rCSI 3.5%
    PRS 32.3%
  • acinar cell of salivary gland CL0002623
    CSI 2.6
    rCSI 59.5%
    PRS 38.8%
  • effector memory CD8-positive, alpha-beta T cell CL0000913
    CSI 2.6
    rCSI 2.3%
    PRS 32.1%
  • brush cell CL0002204
    CSI 2.6
    rCSI 5.2%
    PRS 49.5%
  • intestine goblet cell CL0019031
    CSI 2.6
    rCSI 2.4%
    PRS 21.1%
  • enterocyte of epithelium of large intestine CL0002071
    CSI 2.7
    rCSI 13.9%
    PRS 35.8%
  • cerebral cortex pyramidal neuron CL4023111
    CSI 2.8
    rCSI 16.9%
    PRS 50.2%
  • lung endothelial cell CL1001567
    CSI 2.8
    rCSI 6.5%
    PRS 47.3%
  • central memory CD4-positive, alpha-beta T cell CL0000904
    CSI 2.8
    rCSI 1.7%
    PRS 29.3%

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.
Network Configuration

Explore relationships of the current gene. Select an Interaction Source: 'ONTOLOGY' for shared pathways (GO/Reactome) or 'STRING' for protein-protein interactions. Further refine by selecting context genes and comparing Cell Significance Index (CSI) scores between baseline and target cell types and their specific contexts.

Comma-separated if multiple.
Comma-separated if multiple.

Legend:
  • Query Gene
  • Node Color (Target Cell CSI, relative to current network):
    • Very High
    • High
    • Medium
    • Low
    • Very Low
    • CSI N/A
  • Node Size: Proportional to Target Cell CSI magnitude
  • STRING PPI Edge
  • Shared Pathway Edge (ONTOLOGY)

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Other Information

This section provides additional information about the gene, including a description generated by an AI language model and details about associated proteins.

## Summary [TNRC6A](/details-gene/27327), or Trinucleotide Repeat Containing Adaptor 6A, encodes a key protein component of the RNA-induced silencing complex (RISC). It functions as a critical adaptor protein that links Argonaute proteins, bound to microRNAs (miRNAs), to the cellular machinery responsible for translational repression and mRNA degradation. This role places [TNRC6A](/details-gene/27327) at the heart of post-transcriptional gene regulation. Expression data reveals its high significance across numerous neuronal and glial cell types in the central nervous system, particularly various GABAergic cortical interneurons, suggesting a vital function in maintaining neuronal identity and function. Its localization to cytoplasmic processing bodies (P-bodies), sites of mRNA decay, is well-documented and essential for its function in miRNA-mediated gene silencing ([Link](https://doi.org/10.1261/rna.5810203), [Link](https://doi.org/10.1038/ncb1333)). ## Cellular Roles and Expression Landscape The expression profile of [TNRC6A](/details-gene/27327) highlights its fundamental importance in the central nervous system. **Overall**, it shows exceptionally high significance in a wide array of neuronal subtypes, including [VIP GABAergic cortical interneuron](/details-cell/CL4023016) (CSI: 78.11), [pvalb GABAergic cortical interneuron](/details-cell/CL4023018) (CSI: 76.34), [sst GABAergic cortical interneuron](/details-cell/CL4023017) (CSI: 71.39), and [cerebellar granule cell](/details-cell/CL0001031) (CSI: 52.42). This suggests a critical role in the post-transcriptional regulation that defines the diverse functional identities of these inhibitory and excitatory neurons. Beyond neurons, [TNRC6A](/details-gene/27327) is also a significant marker in several glial and supportive cell populations of the brain, such as [choroid plexus epithelial cell](/details-cell/CL0000706), [Bergmann glial cell](/details-cell/CL0000644), and [astrocyte](/details-cell/CL0000127). Its expression in [differentiation-committed oligodendrocyte precursor](/details-cell/CL4023059) indicates a potential role during glial development and maturation. The gene's activity extends beyond the nervous system, with high significance noted in [cardiac muscle cell](/details-cell/CL0000746) and [adipocyte](/details-cell/CL0000136), pointing to a broad, yet cell-type-specific, requirement for robust miRNA-mediated gene silencing. Conversely, the low to negligible significance of [TNRC6A](/details-gene/27327) in cell types such as [paneth cell](/details-cell/CL0000510), [enteroendocrine cell of colon](/details-cell/CL0009042), and certain immune lineages like [T-helper 1 cell](/details-cell/CL0000545) helps to define its functional specificity, suggesting that other regulatory mechanisms may be more prominent in these particular cellular contexts. ## Pathways and Molecular Function The functional annotations for [TNRC6A](/details-gene/27327) confirm its central role in RNA-mediated gene regulation. It is a key player in [Mirna-mediated post-transcriptional gene silencing](/details-cell/GO:0035195) and [Mirna-mediated gene silencing by inhibition of translation](/details-cell/GO:0035278), consistent with its well-established function within the [RISC complex](/details-cell/GO:0016442). Its molecular function is defined by its ability to act as a [Protein-macromolecule adaptor activity](/details-cell/GO:0030674) and its capacity for [Rna binding](/details-cell/GO:0003723). These functions are executed within distinct cytoplasmic foci known as [P-body](/details-cell/GO:0000932), where it facilitates [P-body assembly](/details-cell/GO:0033962) ([Link](https://doi.org/10.1242/jcs.01477)). The extensive list of Reactome pathways, such as [Signaling by wnt](/details-pathway/R-HSA-195721), [Signaling by notch](/details-pathway/R-HSA-157118), and [Signaling by tgfb family members](/details-pathway/R-HSA-9006936), likely reflects the downstream consequences of [TNRC6A](/details-gene/27327)-mediated silencing. Rather than being a direct component of these pathways, [TNRC6A](/details-gene/27327) regulates their activity by controlling the expression of key pathway components via miRNAs. This is exemplified by its involvement in pathways like [Regulation of pten mrna translation](/details-pathway/R-HSA-8943723) and [Competing endogenous rnas (cernas) regulate pten translation](/details-pathway/R-HSA-8948700), highlighting its specific impact on critical signaling nodes. ## Research Directions The widespread and high-level expression of [TNRC6A](/details-gene/27327) in the CNS, coupled with its fundamental role in gene silencing, suggests it is a master regulator of neural cell biology. The following hypotheses could guide future research: 1. **Hypothesis on Neuronal Identity:** The high significance of [TNRC6A](/details-gene/27327) across diverse interneuron subtypes ([VIP GABAergic cortical interneuron](/details-cell/CL4023016), [pvalb GABAergic cortical interneuron](/details-cell/CL4023018), etc.) suggests it is essential for establishing and maintaining their distinct transcriptional and functional identities. We hypothesize that [TNRC6A](/details-gene/27327) orchestrates the post-transcriptional suppression of a common set of progenitor genes while simultaneously enabling subtype-specific miRNA programs to fine-tune the expression of terminal identity genes. 2. **Hypothesis on Neurodevelopmental Disorders:** Given its role in regulating the translation of numerous signaling pathway components, subtle mutations or expression changes in [TNRC6A](/details-gene/27327) could lead to a global dysregulation of miRNA function in the developing brain. We hypothesize that haploinsufficiency of [TNRC6A](/details-gene/27327) contributes to the etiology of certain neurodevelopmental disorders by disrupting the precise spatiotemporal control of protein synthesis required for proper neuronal migration and circuit formation. **Proposed Experiment:** To test the first hypothesis, a conditional knockout of [TNRC6A](/details-gene/27327) could be generated in cortical interneuron precursors in mice using an Nkx2-1-Cre or Lhx6-Cre driver line. Single-cell RNA sequencing (scRNA-seq) and single-cell ATAC-seq of the adult cortex would be performed to assess whether the diversity of interneuron subtypes is compromised and to identify transcriptional mis-regulation. This could be complemented with electrophysiological recordings to determine if the functional properties of these neurons are altered. **Therapeutic Potential:** As a core component of the essential miRNA silencing machinery, direct systemic inhibition of [TNRC6A](/details-gene/27327) would likely be highly toxic due to widespread pleiotropic effects. Therefore, it is not a viable candidate for direct therapeutic targeting with small molecule inhibitors. However, understanding its specific interactions with disease-relevant miRNAs and their target mRNAs in disorders like epilepsy or schizophrenia could unveil more precise downstream targets for therapeutic intervention. Strategies aimed at modulating specific [TNRC6A](/details-gene/27327)-miRNA-mRNA axes, rather than inhibiting the entire protein, might represent a more feasible long-term therapeutic avenue.

Genular Protein ID: 2715940605

Symbol: TNR6A_HUMAN

Name: Trinucleotide repeat-containing gene 6A protein

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11950943

Title: A phosphorylated cytoplasmic autoantigen, GW182, associates with a unique population of human mRNAs within novel cytoplasmic speckles.

PubMed ID: 11950943

DOI: 10.1091/mbc.01-11-0544

PubMed ID: 17974005

Title: The full-ORF clone resource of the German cDNA consortium.

PubMed ID: 17974005

DOI: 10.1186/1471-2164-8-399

PubMed ID: 15616553

Title: The sequence and analysis of duplication-rich human chromosome 16.

PubMed ID: 15616553

DOI: 10.1038/nature03187

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 9225980

Title: cDNAs with long CAG trinucleotide repeats from human brain.

PubMed ID: 9225980

DOI: 10.1007/s004390050476

PubMed ID: 10819331

Title: Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.

PubMed ID: 10819331

DOI: 10.1093/dnares/7.2.143

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 14598044

Title: Clinical and serological associations of autoantibodies to GW bodies and a novel cytoplasmic autoantigen GW182.

PubMed ID: 14598044

DOI: 10.1007/s00109-003-0495-y

PubMed ID: 13130130

Title: The GW182 protein colocalizes with mRNA degradation associated proteins hDcp1 and hLSm4 in cytoplasmic GW bodies.

PubMed ID: 13130130

DOI: 10.1261/rna.5810203

PubMed ID: 15494374

Title: GW182 is critical for the stability of GW bodies expressed during the cell cycle and cell proliferation.

PubMed ID: 15494374

DOI: 10.1242/jcs.01477

PubMed ID: 15908945

Title: Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies.

PubMed ID: 15908945

DOI: 10.1038/ncb1265

PubMed ID: 16284623

Title: A role for the P-body component GW182 in microRNA function.

PubMed ID: 16284623

DOI: 10.1038/ncb1333

PubMed ID: 16284622

Title: Disruption of GW bodies impairs mammalian RNA interference.

PubMed ID: 16284622

DOI: 10.1038/ncb1334

PubMed ID: 16906129

Title: Formation of GW bodies is a consequence of microRNA genesis.

PubMed ID: 16906129

DOI: 10.1038/sj.embor.7400783

PubMed ID: 17671087

Title: Let-7 microRNA-mediated mRNA deadenylation and translational repression in a mammalian cell-free system.

PubMed ID: 17671087

DOI: 10.1101/gad.1566707

PubMed ID: 17596515

Title: Small interfering RNA-mediated silencing induces target-dependent assembly of GW/P bodies.

PubMed ID: 17596515

DOI: 10.1091/mbc.e07-01-0070

PubMed ID: 19056672

Title: Identification of GW182 and its novel isoform TNGW1 as translational repressors in Ago2-mediated silencing.

PubMed ID: 19056672

DOI: 10.1242/jcs.036905

PubMed ID: 18690212

Title: Prolyl 4-hydroxylation regulates Argonaute 2 stability.

PubMed ID: 18690212

DOI: 10.1038/nature07186

PubMed ID: 18669648

Title: A quantitative atlas of mitotic phosphorylation.

PubMed ID: 18669648

DOI: 10.1073/pnas.0805139105

PubMed ID: 18946079

Title: Localization of double-stranded small interfering RNA to cytoplasmic processing bodies is Ago2 dependent and results in up-regulation of GW182 and Argonaute-2.

PubMed ID: 18946079

DOI: 10.1091/mbc.e08-08-0796

PubMed ID: 19304925

Title: Importance of the C-terminal domain of the human GW182 protein TNRC6C for translational repression.

PubMed ID: 19304925

DOI: 10.1261/rna.1448009

PubMed ID: 19324964

Title: The C-terminal half of human Ago2 binds to multiple GW-rich regions of GW182 and requires GW182 to mediate silencing.

PubMed ID: 19324964

DOI: 10.1261/rna.1229409

PubMed ID: 19383768

Title: The C-terminal domains of human TNRC6A, TNRC6B, and TNRC6C silence bound transcripts independently of Argonaute proteins.

PubMed ID: 19383768

DOI: 10.1261/rna.1606309

PubMed ID: 19690332

Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.

PubMed ID: 19690332

DOI: 10.1126/scisignal.2000007

PubMed ID: 20068231

Title: Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.

PubMed ID: 20068231

DOI: 10.1126/scisignal.2000475

PubMed ID: 21981923

Title: GW182 proteins directly recruit cytoplasmic deadenylase complexes to miRNA targets.

PubMed ID: 21981923

DOI: 10.1016/j.molcel.2011.09.007

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 26134560

Title: Monocyte chemotactic protein-induced protein 1 and 4 form a complex but act independently in regulation of interleukin-6 mRNA degradation.

PubMed ID: 26134560

DOI: 10.1074/jbc.m114.635870

PubMed ID: 28546213

Title: Tudor-SN-mediated endonucleolytic decay of human cell microRNAs promotes G1/S phase transition.

PubMed ID: 28546213

DOI: 10.1126/science.aai9372

PubMed ID: 29507423

Title: Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy.

PubMed ID: 29507423

DOI: 10.1038/s41588-018-0067-2

PubMed ID: 29395067

Title: High-Density Proximity Mapping Reveals the Subcellular Organization of mRNA-Associated Granules and Bodies.

PubMed ID: 29395067

DOI: 10.1016/j.molcel.2017.12.020

PubMed ID: 31400113

Title: KSHV RNA-binding protein ORF57 inhibits P-body formation to promote viral multiplication by interaction with Ago2 and GW182.

PubMed ID: 31400113

DOI: 10.1093/nar/gkz683

Sequence Information:

  • Length: 1962
  • Mass: 210297
  • Checksum: 963C054628E18592
  • Sequence:
  • MRELEAKATK DVERNLSRDL VQEEEQLMEE KKKKKDDKKK KEAAQKKATE QKIKVPEQIK 
    PSVSQPQPAN SNNGTSTATS TNNNAKRATA NNQQPQQQQQ QQQPQQQQPQ QQPQPQPQQQ 
    QPQQQPQALP RYPREVPPRF RHQEHKQLLK RGQHFPVIAA NLGSAVKVLN SQSESSALTN 
    QQPQNNGEVQ NSKNQSDINH STSGSHYENS QRGPVSSTSD SSTNCKNAVV SDLSEKEAWP 
    SAPGSDPELA SECMDADSAS SSESERNITI MASGNTGGEK DGLRNSTGLG SQNKFVVGSS 
    SNNVGHGSST GPWGFSHGAI ISTCQVSVDA PESKSESSNN RMNAWGTVSS SSNGGLNPST 
    LNSASNHGAW PVLENNGLAL KGPVGSGSSG INIQCSTIGQ MPNNQSINSK VSGGSTHGTW 
    GSLQETCESE VSGTQKVSFS GQPQNITTEM TGPNNTTNFM TSSLPNSGSV QNNELPSSNT 
    GAWRVSTMNH PQMQAPSGMN GTSLSHLSNG ESKSGGSYGT TWGAYGSNYS GDKCSGPNGQ 
    ANGDTVNATL MQPGVNGPMG TNFQVNTNKG GGVWESGAAN SQSTSWGSGN GANSGGSRRG 
    WGTPAQNTGT NLPSVEWNKL PSNQHSNDSA NGNGKTFTNG WKSTEEEDQG SATSQTNEQS 
    SVWAKTGGTV ESDGSTESTG RLEEKGTGES QSRDRRKIDQ HTLLQSIVNR TDLDPRVLSN 
    SGWGQTPIKQ NTAWDTETSP RGERKTDNGT EAWGSSATQT FNSGACIDKT SPNGNDTSSV 
    SGWGDPKPAL RWGDSKGSNC QGGWEDDSAA TGMVKSNQWG NCKEEKAAWN DSQKNKQGWG 
    DGQKSSQGWS VSASDNWGET SRNNHWGEAN KKSSSGGSDS DRSVSGWNEL GKTSSFTWGN 
    NINPNNSSGW DESSKPTPSQ GWGDPPKSNQ SLGWGDSSKP VSSPDWNKQQ DIVGSWGIPP 
    ATGKPPGTGW LGGPIPAPAK EEEPTGWEEP SPESIRRKME IDDGTSAWGD PSKYNYKNVN 
    MWNKNVPNGN SRSDQQAQVH QLLTPASAIS NKEASSGSGW GEPWGEPSTP ATTVDNGTSA 
    WGKPIDSGPS WGEPIAAASS TSTWGSSSVG PQALSKSGPK SMQDGWCGDD MPLPGNRPTG 
    WEEEEDVEIG MWNSNSSQEL NSSLNWPPYT KKMSSKGLSG KKRRRERGMM KGGNKQEEAW 
    INPFVKQFSN ISFSRDSPEE NVQSNKMDLS GGMLQDKRME IDKHSLNIGD YNRTVGKGPG 
    SRPQISKESS MERNPYFDKD GIVADESQNM QFMSSQSMKL PPSNSALPNQ ALGSIAGLGM 
    QNLNSVRQNG NPSMFGVGNT AAQPRGMQQP PAQPLSSSQP NLRAQVPPPL LSPQVPVSLL 
    KYAPNNGGLN PLFGPQQVAM LNQLSQLNQL SQISQLQRLL AQQQRAQSQR SVPSGNRPQQ 
    DQQGRPLSVQ QQMMQQSRQL DPNLLVKQQT PPSQQQPLHQ PAMKSFLDNV MPHTTPELQK 
    GPSPINAFSN FPIGLNSNLN VNMDMNSIKE PQSRLRKWTT VDSISVNTSL DQNSSKHGAI 
    SSGFRLEESP FVPYDFMNSS TSPASPPGSI GDGWPRAKSP NGSSSVNWPP EFRPGEPWKG 
    YPNIDPETDP YVTPGSVINN LSINTVREVD HLRDRNSGSS SSLNTTLPST SAWSSIRASN 
    YNVPLSSTAQ STSARNSDSK LTWSPGSVTN TSLAHELWKV PLPPKNITAP SRPPPGLTGQ 
    KPPLSTWDNS PLRIGGGWGN SDARYTPGSS WGESSSGRIT NWLVLKNLTP QIDGSTLRTL 
    CMQHGPLITF HLNLPHGNAL VRYSSKEEVV KAQKSLHMCV LGNTTILAEF ASEEEISRFF 
    AQSQSLTPSP GWQSLGSSQS RLGSLDCSHS FSSRTDLNHW NGAGLSGTNC GDLHGTSLWG 
    TPHYSTSLWG PPSSSDPRGI SSPSPINAFL SVDHLGGGGE SM