BrainStars multi-state genes (CPu medial:up)
Genes in a specific state at a specific region.
751 - 775 of 3633 entries
| Probe set ID | Symbol | Name |
Regions ![[asc]](http://brainstars.org/static/images/asc2.png) |
Gene Category | |
|---|---|---|---|---|---|
| 751 | 1433557_at | Cbx7 | chromobox homolog 7 | 9 | |
| 752 | 1434066_at | Gtf3c1 | general transcription factor III C 1 | 9 | |
| 753 | 1434248_at | Prkch | protein kinase C, eta | 9 | |
| 754 | 1434883_at | Mtdh | Metadherin | 9 | |
| 755 | 1436672_at | 9 | |||
| 756 | 1436799_at | Enox1 | ecto-NOX disulfide-thiol exchanger 1 | 9 | |
| 757 | 1437067_at | Phtf2 | putative homeodomain transcription factor 2 | 9 | |
| 758 | 1437643_at | Cenpj | centromere protein J | 9 | TF |
| 759 | 1437835_a_at | 0610011L14Rik | RIKEN cDNA 0610011L14 gene | 9 | |
| 760 | 1438497_at | Mfsd8 | major facilitator superfamily domain containing 8 | 9 | |
| 761 | 1438506_s_at | Abi1 | abl-interactor 1 | 9 | |
| 762 | 1438802_at | Foxp1 | forkhead box P1 | 9 | TF Fox |
| 763 | 1439019_at | Fras1 | Fraser syndrome 1 homolog (human) | 9 | EM |
| 764 | 1439239_at | Lin7b | lin-7 homolog B (C. elegans) | 9 | |
| 765 | 1439291_at | 9 | |||
| 766 | 1439501_at | Cbara1 | calcium binding atopy-related autoantigen 1 | 9 | |
| 767 | 1439630_x_at | Sbsn | suprabasin | 9 | |
| 768 | 1439958_at | 100038982 | predicted gene, 100038982 | 9 | |
| 769 | 1439985_at | Abcc12 | ATP-binding cassette, sub-family C (CFTR/MRP), member 12 | 9 | |
| 770 | 1440287_at | 9 | |||
| 771 | 1440452_at | Drp2 | dystrophin related protein 2 | 9 | SP |
| 772 | 1441468_at | ENSMUSG00000074517 | predicted gene, ENSMUSG00000074517 | 9 | |
| 773 | 1442407_at | 9 | |||
| 774 | 1443990_at | Ntrk1 | neurotrophic tyrosine kinase, receptor, type 1 | 9 | NH/NT |
| 775 | 1444104_at | 9 |
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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