BrainStars one-state genes
One-state genes with variable (high variability score) or stable (low variability score) expression patterns
7626 - 7650 of 18904 entries
Probe set ID | Variability score | Variability rank | Mean | Standard Deviation | Present regions | Symbol |
Name ![]() |
Gene Category | |
---|---|---|---|---|---|---|---|---|---|
7626 | 1431960_at | -0.0828029 | 11028 | 8.08465 | 0.22686 | 40 | Wwox | WW domain-containing oxidoreductase | |
7627 | 1431942_at | -0.817421 | 18389 | 7.14717 | 0.0898844 | 3 | Wwox | WW domain-containing oxidoreductase | |
7628 | 1427261_at | 0.502138 | 3727 | 8.76288 | 0.443598 | 48 | Wwc1 | WW, C2 and coiled-coil domain containing 1 | |
7629 | 1420008_s_at | 0.217351 | 6617 | 9.52897 | 0.346046 | 46 | Wwc1 | WW, C2 and coiled-coil domain containing 1 | |
7630 | 1417197_at | 0.426881 | 4381 | 6.90884 | 0.294417 | 1 | Wwc2 | WW, C2 and coiled-coil domain containing 2 | |
7631 | 1448611_at | 0.0639067 | 8729 | 9.38774 | 0.297201 | 48 | Wwc2 | WW, C2 and coiled-coil domain containing 2 | |
7632 | 1416281_at | -0.77421 | 18255 | 10.4444 | 0.129689 | 48 | Wdr45l | Wdr45 like | |
7633 | 1448376_at | 0.0595577 | 8793 | 9.51799 | 0.29566 | 48 | Wrnip1 | Werner helicase interacting protein 1 | |
7634 | 1425074_at | -0.364908 | 14975 | 7.58265 | 0.15633 | 46 | Wrn | Werner syndrome homolog (human) | |
7635 | 1423575_a_at | -0.775392 | 18260 | 8.80116 | 0.124141 | 48 | Wbscr22 | Williams Beuren syndrome chromosome region 22 | |
7636 | 1418359_at | -0.148154 | 11969 | 8.57776 | 0.228781 | 2 | Wbscr27 | Williams Beuren syndrome chromosome region 27 (human) | |
7637 | 1454805_at | 0.327335 | 5362 | 9.29904 | 0.385355 | 48 | Wtap | Wilms' tumour 1-associating protein | |
7638 | 1452401_at | -0.0247779 | 10133 | 10.2323 | 0.276102 | 48 | Wtap | Wilms' tumour 1-associating protein | |
7639 | 1419631_at | -0.291458 | 14029 | 7.11489 | 0.150165 | 6 | Was | Wiskott-Aldrich syndrome homolog (human) | |
7640 | 1426777_a_at | 0.335101 | 5285 | 9.46859 | 0.389456 | 48 | Wasl | Wiskott-Aldrich syndrome-like (human) | |
7641 | 1452193_a_at | 0.0793005 | 8507 | 9.7964 | 0.304235 | 48 | Wasl | Wiskott-Aldrich syndrome-like (human) | |
7642 | 1432155_at | -0.497173 | 16401 | 7.21133 | 0.124504 | 7 | Wasl | Wiskott-Aldrich syndrome-like (human) | |
7643 | 1435136_at | 0.0193978 | 9428 | 8.9032 | 0.277399 | 47 | Whsc1 | Wolf-Hirschhorn syndrome candidate 1 (human) | |
7644 | 1443741_x_at | -0.0585399 | 10660 | 7.77646 | 0.218503 | 19 | Whsc1 | Wolf-Hirschhorn syndrome candidate 1 (human) | |
7645 | 1455228_at | -0.0700924 | 10851 | 9.42111 | 0.260002 | 48 | Whsc1 | Wolf-Hirschhorn syndrome candidate 1 (human) | |
7646 | 1457793_a_at | 0.22737 | 6492 | 7.73012 | 0.286868 | 47 | Whsc1l1 | Wolf-Hirschhorn syndrome candidate 1-like 1 (human) | |
7647 | 1455668_at | 0.0257842 | 9317 | 9.281 | 0.28473 | 48 | Whsc1l1 | Wolf-Hirschhorn syndrome candidate 1-like 1 (human) | |
7648 | 1457794_at | 0.0219896 | 9381 | 6.17095 | 0.156967 | 42 | Whsc1l1 | Wolf-Hirschhorn syndrome candidate 1-like 1 (human) | |
7649 | 1427248_at | 0.0415207 | 9082 | 9.22448 | 0.289159 | 48 | Whsc2 | Wolf-Hirschhorn syndrome candidate 2 (human) | |
7650 | 1425928_at | 0.858343 | 1535 | 8.63462 | 0.631896 | 20 | Xkr6 | X Kell blood group precursor related family member 6 homolog |
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