BrainStars multi-state genes (Cx cingulate:low)
Genes in a specific state at a specific region.
451 - 475 of 8980 entries
Probe set ID ![[asc]](http://brainstars.org/static/images/asc2.png) |
Symbol | Name | Regions | Gene Category | |
|---|---|---|---|---|---|
| 451 | 1417817_a_at | Wwtr1 | WW domain containing transcription regulator 1 | 43 | TF |
| 452 | 1417821_at | D17H6S56E-5 | DNA segment, Chr 17, human D6S56E 5 | 46 | SP |
| 453 | 1417822_at | D17H6S56E-5 | DNA segment, Chr 17, human D6S56E 5 | 46 | SP |
| 454 | 1417830_at | Smc1a | structural maintenance of chromosomes 1A | 46 | |
| 455 | 1417835_at | Mug1 | murinoglobulin 1 | 47 | |
| 456 | 1417836_at | Gpx7 | glutathione peroxidase 7 | 43 | |
| 457 | 1417839_at | Cldn5 | claudin 5 | 45 | CA SP |
| 458 | 1417842_at | Caml | calcium modulating ligand | 44 | |
| 459 | 1417843_s_at | Eps8l2 | EPS8-like 2 | 42 | |
| 460 | 1417850_at | Rb1 | retinoblastoma 1 | 45 | TF |
| 461 | 1417851_at | Cxcl13 | chemokine (C-X-C motif) ligand 13 | 47 | |
| 462 | 1417853_at | Clca1 | chloride channel calcium activated 1 | 46 | Ch |
| 463 | 1417856_at | Relb | avian reticuloendotheliosis viral (v-rel) oncogene related B | 44 | TF |
| 464 | 1417857_at | Mmaa | methylmalonic aciduria (cobalamin deficiency) type A | 39 | |
| 465 | 1417862_at | Fam181b | family with sequence similarity 181, member B | 31 | |
| 466 | 1417866_at | Tnfaip1 | tumor necrosis factor, alpha-induced protein 1 (endothelial) | 29 | Ch |
| 467 | 1417871_at | Hsd17b7 | hydroxysteroid (17-beta) dehydrogenase 7 | 42 | |
| 468 | 1417876_at | Fcgr1 | Fc receptor, IgG, high affinity I | 47 | |
| 469 | 1417879_at | Nenf | neuron derived neurotrophic factor | 34 | |
| 470 | 1417884_at | Slc16a6 | solute carrier family 16 (monocarboxylic acid transporters), member 6 | 31 | |
| 471 | 1417886_at | 1810009A15Rik | RIKEN cDNA 1810009A15 gene | 45 | |
| 472 | 1417889_at | Apobec2 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 | 47 | |
| 473 | 1417902_at | Slc19a2 | solute carrier family 19 (thiamine transporter), member 2 | 44 | GPCR SLC |
| 474 | 1417903_at | Dfna5 | deafness, autosomal dominant 5 (human) | 47 | |
| 475 | 1417910_at | Ccna2 | cyclin A2 | 35 |
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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