SYMBOL | TITLE | MIN | MAX | NCBI
human
gene
summary |
2310035C23RIK | RIKEN cDNA 2310035C23 gene | 6.91 | 9.40 | NCBI mm gene   |
4930432O21RIK | RIKEN cDNA 4930432O21 gene | 5.05 | 8.71 | NCBI mm gene   |
4931406H21RIK | RIKEN cDNA 4931406H21 gene | 5.60 | 8.08 | NCBI mm gene   |
6720487G11RIK | zinc finger protein 738 | 5.18 | 8.26 | NCBI mm gene   |
A230046K03RIK | RIKEN cDNA A230046K03 gene | 6.86 | 10.34 | NCBI mm gene   |
AFTPH | aftiphilin | 7.39 | 11.41 | NCBI mm gene   |
APC | adenomatosis polyposis coli | 6.20 | 9.87 | NCBI mm gene  Summary: This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway. It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product. [provided by RefSeq]. |
ARID4A | AT rich interactive domain 4A (RBP1-like) | 6.04 | 9.92 | NCBI mm gene   |
ATAD2B | ATPase family, AAA domain containing 2B | 6.79 | 9.89 | NCBI mm gene   |
B430203M17RIK | phosphatase and tensin homolog | 4.79 | 9.43 | NCBI mm gene   |
CEP350 | centrosomal protein 350 | 6.87 | 10.69 | NCBI mm gene   |
CLK1 | CDC-like kinase 1 | 8.42 | 12.01 | NCBI mm gene   |
GM10397 | predicted gene 10397 | 8.10 | 11.26 | NCBI mm gene   |
JMJD1C | jumonji domain containing 1C | 6.79 | 11.55 | NCBI mm gene   |
NR3C1 | nuclear receptor subfamily 3, group C, member 1 | 7.07 | 10.20 | NCBI mm gene  Summary: The protein encoded by this gene is a receptor for glucocorticoids that can act as both a transcription factor and as a regulator of other transcription factors. This protein can also be found in heteromeric cytoplasmic complexes along with heat shock factors and immunophilins. The protein is typically found in the cytoplasm until it binds a ligand, which induces transport into the nucleus. Mutations in this gene are a cause of glucocorticoid resistance, or cortisol, resistance. Alternate splicing, the use of at least three different promoters, and alternate translation initiation sites result in several transcript variants encoding the same protein or different isoforms, but the full-length nature of some variants has not been determined. [provided by RefSeq]. |
ROCK2 | Rho-associated coiled-coil containing protein kinase 2 | 5.98 | 9.92 | NCBI mm gene   |
SETDB2 | SET domain, bifurcated 2 | 4.38 | 9.65 | NCBI mm gene   |
SLK | STE20-like kinase (yeast) | 7.27 | 10.69 | NCBI mm gene   |
TAOK1 | TAO kinase 1 | 6.89 | 10.34 | NCBI mm gene   |
VPS13B | vacuolar protein sorting 13B (yeast) | 7.16 | 10.11 | NCBI mm gene  Summary: This gene encodes a potential transmembrane protein that may function in vesicle-mediated transport and sorting of proteins within the cell. This protein may play a role in the development and the function of the eye, hematological system, and central nervous system. Mutations in this gene have been associated with Cohen syndrome. Multiple splice variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq]. |
ZC3H7A | zinc finger CCCH type containing 7 A | 7.29 | 10.42 | NCBI mm gene   |
ZFC3H1 | zinc finger, C3H1-type containing | 6.49 | 11.76 | NCBI mm gene   |
ZFP62 | zinc finger protein 62 | 5.98 | 9.56 | NCBI mm gene   |
ZUFSP | zinc finger with UFM1-specific peptidase domain | 5.61 | 10.25 | NCBI mm gene   |