BrainStars multi-state genes (Pir:down)
Genes in a specific state at a specific region.
551 - 575 of 9870 entries
Probe set ID ![[asc]](http://brainstars.org/static/images/asc2.png) |
Symbol | Name | Regions | Gene Category | |
|---|---|---|---|---|---|
| 551 | 1417830_at | Smc1a | structural maintenance of chromosomes 1A | 46 | |
| 552 | 1417835_at | Mug1 | murinoglobulin 1 | 47 | |
| 553 | 1417836_at | Gpx7 | glutathione peroxidase 7 | 43 | |
| 554 | 1417837_at | Phlda2 | pleckstrin homology-like domain, family A, member 2 | 9 | |
| 555 | 1417839_at | Cldn5 | claudin 5 | 45 | CA SP |
| 556 | 1417842_at | Caml | calcium modulating ligand | 44 | |
| 557 | 1417843_s_at | Eps8l2 | EPS8-like 2 | 46 | |
| 558 | 1417850_at | Rb1 | retinoblastoma 1 | 47 | TF |
| 559 | 1417851_at | Cxcl13 | chemokine (C-X-C motif) ligand 13 | 47 | |
| 560 | 1417852_x_at | Clca1 | chloride channel calcium activated 1 | 46 | Ch |
| 561 | 1417853_at | Clca1 | chloride channel calcium activated 1 | 46 | Ch |
| 562 | 1417856_at | Relb | avian reticuloendotheliosis viral (v-rel) oncogene related B | 44 | TF |
| 563 | 1417857_at | Mmaa | methylmalonic aciduria (cobalamin deficiency) type A | 39 | |
| 564 | 1417859_at | Gas7 | growth arrest specific 7 | 46 | Ng |
| 565 | 1417862_at | Fam181b | family with sequence similarity 181, member B | 46 | |
| 566 | 1417871_at | Hsd17b7 | hydroxysteroid (17-beta) dehydrogenase 7 | 42 | |
| 567 | 1417874_at | Tmem9b | TMEM9 domain family, member B | 3 | |
| 568 | 1417876_at | Fcgr1 | Fc receptor, IgG, high affinity I | 47 | |
| 569 | 1417877_at | Eepd1 | endonuclease/exonuclease/phosphatase family domain containing 1 | 43 | |
| 570 | 1417879_at | Nenf | neuron derived neurotrophic factor | 34 | |
| 571 | 1417884_at | Slc16a6 | solute carrier family 16 (monocarboxylic acid transporters), member 6 | 44 | |
| 572 | 1417886_at | 1810009A15Rik | RIKEN cDNA 1810009A15 gene | 45 | |
| 573 | 1417889_at | Apobec2 | apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2 | 47 | |
| 574 | 1417902_at | Slc19a2 | solute carrier family 19 (thiamine transporter), member 2 | 47 | GPCR SLC |
| 575 | 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