BrainStars (B*)

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BrainStars multi-state genes (CA1:low)

Genes in a specific state at a specific region. (Help)
High state regions Up state regions Low state regions Down state regions
LS RS Cx motor Cx cingulate OB anterior OB posterior Pir Tu ventral S CA1 CA2/CA3 DG A anterior A posterior GP CPu lateral CPu medial MD VA/VL VPM/VPL LG MG Hb M ME SCN MPA SO Pa SPa ventral SPa dorsal DM VMH Arc LH PAG SC IC VTA SN Tg Pn MVe Cb vermis Cb lobe Cb nucleus spinal cord anterior spinal cord posterior
451 - 475 of 8779 entries
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Probe set ID [asc] Symbol Name Regions Gene Category
451 1417822_at [new page][PP page] D17H6S56E-5 DNA segment, Chr 17, human D6S56E 5 46 SP
452 1417830_at [new page][PP page] Smc1a structural maintenance of chromosomes 1A 46
453 1417835_at [new page][PP page] Mug1 murinoglobulin 1 47
454 1417836_at [new page][PP page] Gpx7 glutathione peroxidase 7 43
455 1417837_at [new page][PP page] Phlda2 pleckstrin homology-like domain, family A, member 2 9
456 1417839_at [new page][PP page] Cldn5 claudin 5 45 CA SP
457 1417842_at [new page][PP page] Caml calcium modulating ligand 44
458 1417843_s_at [new page][PP page] Eps8l2 EPS8-like 2 42
459 1417851_at [new page][PP page] Cxcl13 chemokine (C-X-C motif) ligand 13 47
460 1417852_x_at [new page][PP page] Clca1 chloride channel calcium activated 1 38 Ch
461 1417853_at [new page][PP page] Clca1 chloride channel calcium activated 1 46 Ch
462 1417857_at [new page][PP page] Mmaa methylmalonic aciduria (cobalamin deficiency) type A 39
463 1417862_at [new page][PP page] Fam181b family with sequence similarity 181, member B 31
464 1417871_at [new page][PP page] Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 42
465 1417876_at [new page][PP page] Fcgr1 Fc receptor, IgG, high affinity I 47
466 1417879_at [new page][PP page] Nenf neuron derived neurotrophic factor 34
467 1417886_at [new page][PP page] 1810009A15Rik RIKEN cDNA 1810009A15 gene 45
468 1417889_at [new page][PP page] Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 47
469 1417891_at [new page][PP page] Spsb3 splA/ryanodine receptor domain and SOCS box containing 3 26
470 1417902_at [new page][PP page] Slc19a2 solute carrier family 19 (thiamine transporter), member 2 44 GPCR SLC
471 1417903_at [new page][PP page] Dfna5 deafness, autosomal dominant 5 (human) 47
472 1417910_at [new page][PP page] Ccna2 cyclin A2 35
473 1417917_at [new page][PP page] Cnn1 calponin 1 45
474 1417919_at [new page][PP page] Ppp1r7 protein phosphatase 1, regulatory (inhibitor) subunit 7 45
475 1417931_at [new page][PP page] Ndst2 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2 46
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TF=Transcription Factor; Ch=Channel; GPCR=GPCR; CA=Cell Adhesion; EM=Extracellular Matrix; SP=Structural Protein; Ng=Neurogenesis; Hox=Homeobox; NR=Nuclear Receptor; NH/NT=NH/NT; AG=Axon Guidance; SLC=SLC Transporter; Fox=Forkhead
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