BrainStars multi-state genes (ME:down)
Genes in a specific state at a specific region.
426 - 450 of 8965 entries
Probe set ID ![[asc]](http://brainstars.org/static/images/asc2.png) |
Symbol | Name | Regions | Gene Category | |
|---|---|---|---|---|---|
| 426 | 1417804_at | Rasgrp2 | RAS, guanyl releasing protein 2 | 46 | |
| 427 | 1417809_at | Slc22a18 | solute carrier family 22 (organic cation transporter), member 18 | 47 | |
| 428 | 1417830_at | Smc1a | structural maintenance of chromosomes 1A | 46 | |
| 429 | 1417835_at | Mug1 | murinoglobulin 1 | 47 | |
| 430 | 1417839_at | Cldn5 | claudin 5 | 45 | CA SP |
| 431 | 1417843_s_at | Eps8l2 | EPS8-like 2 | 46 | |
| 432 | 1417850_at | Rb1 | retinoblastoma 1 | 47 | TF |
| 433 | 1417851_at | Cxcl13 | chemokine (C-X-C motif) ligand 13 | 47 | |
| 434 | 1417852_x_at | Clca1 | chloride channel calcium activated 1 | 46 | Ch |
| 435 | 1417853_at | Clca1 | chloride channel calcium activated 1 | 46 | Ch |
| 436 | 1417857_at | Mmaa | methylmalonic aciduria (cobalamin deficiency) type A | 39 | |
| 437 | 1417858_at | Rasal1 | RAS protein activator like 1 (GAP1 like) | 38 | |
| 438 | 1417859_at | Gas7 | growth arrest specific 7 | 46 | Ng |
| 439 | 1417862_at | Fam181b | family with sequence similarity 181, member B | 46 | |
| 440 | 1417871_at | Hsd17b7 | hydroxysteroid (17-beta) dehydrogenase 7 | 42 | |
| 441 | 1417874_at | Tmem9b | TMEM9 domain family, member B | 3 | |
| 442 | 1417876_at | Fcgr1 | Fc receptor, IgG, high affinity I | 47 | |
| 443 | 1417877_at | Eepd1 | endonuclease/exonuclease/phosphatase family domain containing 1 | 43 | |
| 444 | 1417884_at | Slc16a6 | solute carrier family 16 (monocarboxylic acid transporters), member 6 | 44 | |
| 445 | 1417889_at | Apobec2 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 | 47 | |
| 446 | 1417891_at | Spsb3 | splA/ryanodine receptor domain and SOCS box containing 3 | 26 | |
| 447 | 1417893_at | Sfxn3 | sideroflexin 3 | 43 | |
| 448 | 1417901_a_at | Ica1 | islet cell autoantigen 1 | 5 | |
| 449 | 1417902_at | Slc19a2 | solute carrier family 19 (thiamine transporter), member 2 | 47 | GPCR SLC |
| 450 | 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