BrainStars (B*)

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BrainStars multi-state genes (Pir: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
501 - 525 of 8942 entries
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Probe set ID [asc] Symbol Name Regions Gene Category
501 1417830_at [new page][PP page] Smc1a structural maintenance of chromosomes 1A 46
502 1417835_at [new page][PP page] Mug1 murinoglobulin 1 47
503 1417836_at [new page][PP page] Gpx7 glutathione peroxidase 7 43
504 1417837_at [new page][PP page] Phlda2 pleckstrin homology-like domain, family A, member 2 9
505 1417839_at [new page][PP page] Cldn5 claudin 5 45 CA SP
506 1417842_at [new page][PP page] Caml calcium modulating ligand 44
507 1417843_s_at [new page][PP page] Eps8l2 EPS8-like 2 42
508 1417850_at [new page][PP page] Rb1 retinoblastoma 1 45 TF
509 1417851_at [new page][PP page] Cxcl13 chemokine (C-X-C motif) ligand 13 47
510 1417852_x_at [new page][PP page] Clca1 chloride channel calcium activated 1 38 Ch
511 1417853_at [new page][PP page] Clca1 chloride channel calcium activated 1 46 Ch
512 1417856_at [new page][PP page] Relb avian reticuloendotheliosis viral (v-rel) oncogene related B 44 TF
513 1417857_at [new page][PP page] Mmaa methylmalonic aciduria (cobalamin deficiency) type A 39
514 1417862_at [new page][PP page] Fam181b family with sequence similarity 181, member B 31
515 1417871_at [new page][PP page] Hsd17b7 hydroxysteroid (17-beta) dehydrogenase 7 42
516 1417874_at [new page][PP page] Tmem9b TMEM9 domain family, member B 3
517 1417876_at [new page][PP page] Fcgr1 Fc receptor, IgG, high affinity I 47
518 1417879_at [new page][PP page] Nenf neuron derived neurotrophic factor 34
519 1417884_at [new page][PP page] Slc16a6 solute carrier family 16 (monocarboxylic acid transporters), member 6 31
520 1417886_at [new page][PP page] 1810009A15Rik RIKEN cDNA 1810009A15 gene 45
521 1417889_at [new page][PP page] Apobec2 apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 47
522 1417902_at [new page][PP page] Slc19a2 solute carrier family 19 (thiamine transporter), member 2 44 GPCR SLC
523 1417903_at [new page][PP page] Dfna5 deafness, autosomal dominant 5 (human) 47
524 1417910_at [new page][PP page] Ccna2 cyclin A2 35
525 1417917_at [new page][PP page] Cnn1 calponin 1 45
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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
Copyright © 2009 RIKEN Center for developmental Biology.