BrainStars multi-state genes (VPM/VPL:low)
Genes in a specific state at a specific region.
476 - 500 of 9353 entries
Probe set ID ![[asc]](http://brainstars.org/static/images/asc2.png) |
Symbol | Name | Regions | Gene Category | |
|---|---|---|---|---|---|
| 476 | 1417817_a_at | Wwtr1 | WW domain containing transcription regulator 1 | 43 | TF |
| 477 | 1417821_at | D17H6S56E-5 | DNA segment, Chr 17, human D6S56E 5 | 46 | SP |
| 478 | 1417822_at | D17H6S56E-5 | DNA segment, Chr 17, human D6S56E 5 | 46 | SP |
| 479 | 1417830_at | Smc1a | structural maintenance of chromosomes 1A | 46 | |
| 480 | 1417835_at | Mug1 | murinoglobulin 1 | 47 | |
| 481 | 1417836_at | Gpx7 | glutathione peroxidase 7 | 43 | |
| 482 | 1417839_at | Cldn5 | claudin 5 | 45 | CA SP |
| 483 | 1417842_at | Caml | calcium modulating ligand | 44 | |
| 484 | 1417850_at | Rb1 | retinoblastoma 1 | 45 | TF |
| 485 | 1417851_at | Cxcl13 | chemokine (C-X-C motif) ligand 13 | 47 | |
| 486 | 1417852_x_at | Clca1 | chloride channel calcium activated 1 | 38 | Ch |
| 487 | 1417853_at | Clca1 | chloride channel calcium activated 1 | 46 | Ch |
| 488 | 1417856_at | Relb | avian reticuloendotheliosis viral (v-rel) oncogene related B | 44 | TF |
| 489 | 1417857_at | Mmaa | methylmalonic aciduria (cobalamin deficiency) type A | 39 | |
| 490 | 1417858_at | Rasal1 | RAS protein activator like 1 (GAP1 like) | 38 | |
| 491 | 1417859_at | Gas7 | growth arrest specific 7 | 25 | Ng |
| 492 | 1417862_at | Fam181b | family with sequence similarity 181, member B | 31 | |
| 493 | 1417866_at | Tnfaip1 | tumor necrosis factor, alpha-induced protein 1 (endothelial) | 29 | Ch |
| 494 | 1417871_at | Hsd17b7 | hydroxysteroid (17-beta) dehydrogenase 7 | 42 | |
| 495 | 1417876_at | Fcgr1 | Fc receptor, IgG, high affinity I | 47 | |
| 496 | 1417879_at | Nenf | neuron derived neurotrophic factor | 34 | |
| 497 | 1417886_at | 1810009A15Rik | RIKEN cDNA 1810009A15 gene | 45 | |
| 498 | 1417889_at | Apobec2 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 | 47 | |
| 499 | 1417902_at | Slc19a2 | solute carrier family 19 (thiamine transporter), member 2 | 44 | GPCR SLC |
| 500 | 1417903_at | Dfna5 | deafness, autosomal dominant 5 (human) | 47 |
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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