BrainStars switch-like genes (CPu medial:down)
Genes in a specific state at a specific region.
376 - 400 of 9623 entries
| Probe set ID | Symbol | Name | Regions |
Gene Category ![[asc]](http://www.brainstars.org/static/images/asc2.png) |
|
|---|---|---|---|---|---|
| 376 | 1417787_at | Dkkl1 | dickkopf-like 1 | 44 | |
| 377 | 1417788_at | Sncg | synuclein, gamma | 44 | |
| 378 | 1417789_at | Ccl11 | chemokine (C-C motif) ligand 11 | 47 | |
| 379 | 1417790_at | Dok1 | docking protein 1 | 46 | |
| 380 | 1417793_at | Iigp2 | interferon inducible GTPase 2 | 47 | |
| 381 | 1417797_a_at | 1810019J16Rik | RIKEN cDNA 1810019J16 gene | 46 | |
| 382 | 1417802_at | 1110032A04Rik | RIKEN cDNA 1110032A04 gene | 45 | |
| 383 | 1417803_at | 1110032A04Rik | RIKEN cDNA 1110032A04 gene | 45 | |
| 384 | 1417809_at | Slc22a18 | solute carrier family 22 (organic cation transporter), member 18 | 47 | |
| 385 | 1417814_at | Pla2g5 | phospholipase A2, group V | 47 | |
| 386 | 1417830_at | Smc1a | structural maintenance of chromosomes 1A | 46 | |
| 387 | 1417835_at | Mug1 | murinoglobulin 1 | 47 | |
| 388 | 1417836_at | Gpx7 | glutathione peroxidase 7 | 43 | |
| 389 | 1417842_at | Caml | calcium modulating ligand | 44 | |
| 390 | 1417843_s_at | Eps8l2 | EPS8-like 2 | 46 | |
| 391 | 1417851_at | Cxcl13 | chemokine (C-X-C motif) ligand 13 | 47 | |
| 392 | 1417858_at | Rasal1 | RAS protein activator like 1 (GAP1 like) | 38 | |
| 393 | 1417862_at | Fam181b | family with sequence similarity 181, member B | 46 | |
| 394 | 1417871_at | Hsd17b7 | hydroxysteroid (17-beta) dehydrogenase 7 | 42 | |
| 395 | 1417876_at | Fcgr1 | Fc receptor, IgG, high affinity I | 47 | |
| 396 | 1417879_at | Nenf | neuron derived neurotrophic factor | 34 | |
| 397 | 1417884_at | Slc16a6 | solute carrier family 16 (monocarboxylic acid transporters), member 6 | 44 | |
| 398 | 1417886_at | 1810009A15Rik | RIKEN cDNA 1810009A15 gene | 45 | |
| 399 | 1417889_at | Apobec2 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 | 47 | |
| 400 | 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