| SYMBOL | TITLE | MIN | MAX | NCBI
human
gene
summary |
|---|
| 1810007M14RIK | GC-rich sequence DNA-binding factor 1 | 6.93 | 10.29 | NCBI mm gene |
| A530032D15RIK | RIKEN cDNA A530032D15Rik gene | 7.55 | 10.70 | NCBI mm gene |
| ARHGEF12 | Rho guanine nucleotide exchange factor (GEF) 12 | 5.90 | 10.12 | NCBI mm gene |
| BAZ1A | bromodomain adjacent to zinc finger domain 1A | 7.71 | 10.96 | NCBI mm gene |
| BAZ2B | bromodomain adjacent to zinc finger domain, 2B | 5.91 | 9.92 | NCBI mm gene |
| C130026I21RIK | RIKEN cDNA C130026I21 gene | 5.67 | 9.38 | NCBI mm gene |
| C530030P08RIK | RIKEN cDNA C530030P08 gene | 8.80 | 12.90 | NCBI mm gene |
| CCNL1 | cyclin L1 | 7.83 | 11.67 | NCBI mm gene |
| CD2AP | CD2-associated protein | 5.83 | 11.22 | NCBI mm gene Summary: This gene encodes a scaffolding molecule that regulates the actin cytoskeleton. The protein directly interacts with filamentous actin and a variety of cell membrane proteins through multiple actin binding sites, SH3 domains, and a proline-rich region containing binding sites for SH3 domains. The cytoplasmic protein localizes to membrane ruffles, lipid rafts, and the leading edges of cells. It is implicated in dynamic actin remodeling and membrane trafficking that occurs during receptor endocytosis and cytokinesis. Haploinsufficiency of this gene is implicated in susceptibility to glomerular disease. [provided by RefSeq]. |
| CEP170 | centrosomal protein 170 | 5.99 | 9.93 | NCBI mm gene |
| CSPRS | component of Sp100-rs | 4.26 | 10.61 | NCBI mm gene |
| DCLRE1C | DNA cross-link repair 1C, PSO2 homolog (S. cerevisiae) | 5.99 | 9.97 | NCBI mm gene Summary: This gene encodes a nuclear protein that is involved in V(D)J recombination and DNA repair. The protein has single-strand-specific 5'-3' exonuclease activity; it also exhibits endonuclease activity on 5' and 3' overhangs and hairpins when complexed with protein kinase, DNA-activated, catalytic polypeptide. Mutations in this gene cause Athabascan-type severe combined immunodeficiency (SCIDA). [provided by RefSeq]. |
| EIF2AK4 | eukaryotic translation initiation factor 2 alpha kinase 4 | 5.91 | 8.77 | NCBI mm gene |
| ELL2 | elongation factor RNA polymerase II 2 | 5.29 | 9.75 | NCBI mm gene |
| EPB4.1L2 | erythrocyte protein band 4.1-like 2 | 6.88 | 11.05 | NCBI mm gene |
| FEM1C | fem-1 homolog c (C.elegans) | 7.78 | 11.13 | NCBI mm gene |
| GDAP10 | ganglioside-induced differentiation-associated-protein 10 | 5.05 | 10.62 | NCBI mm gene |
| GM13570 | predicted gene 13570 | 5.71 | 8.51 | NCBI mm gene |
| HIVEP1 | human immunodeficiency virus type I enhancer binding protein 1 | 7.10 | 11.51 | NCBI mm gene |
| HSN2 | hereditary sensory neuropathy, type II | 6.07 | 11.67 | NCBI mm gene |
| IQGAP1 | IQ motif containing GTPase activating protein 1 | 6.37 | 12.22 | NCBI mm gene |
| KBTBD7 | kelch repeat and BTB (POZ) domain containing 7 | 5.27 | 10.03 | NCBI mm gene |
| MALT1 | mucosa associated lymphoid tissue lymphoma translocation gene 1 | 6.95 | 11.92 | NCBI mm gene |
| MYO9A | myosin IXa | 5.62 | 12.23 | NCBI mm gene |
| PAPD4 | PAP associated domain containing 4 | 8.51 | 11.03 | NCBI mm gene |
| PRDM9 | PR domain containing 9 | 5.24 | 7.48 | NCBI mm gene |
| RFWD2 | ring finger and WD repeat domain 2 | 7.15 | 10.11 | NCBI mm gene |
| RUFY3 | RUN and FYVE domain containing 3 | 5.64 | 8.54 | NCBI mm gene |
| SDCCAG8 | serologically defined colon cancer antigen 8 | 6.14 | 9.27 | NCBI mm gene |
| SP140 | Sp140 nuclear body protein | 6.41 | 10.68 | NCBI mm gene |
| SPAG9 | sperm associated antigen 9 | 6.95 | 10.81 | NCBI mm gene |
| TET2 | tet oncogene family member 2 | 6.26 | 10.16 | NCBI mm gene |
| THAP6 | THAP domain containing 6 | 5.60 | 9.75 | NCBI mm gene |
| TMEM131 | transmembrane protein 131 | 7.49 | 11.46 | NCBI mm gene |
| TRPS1 | trichorhinophalangeal syndrome I (human) | 5.37 | 10.92 | NCBI mm gene Summary: This gene encodes a transcription factor that represses GATA-regulated genes and binds to a dynein light chain protein. Binding of the encoded protein to the dynein light chain protein affects binding to GATA consensus sequences and suppresses its transcriptional activity. Defects in this gene are a cause of tricho-rhino-phalangeal syndrome (TRPS) types I-III. [provided by RefSeq]. |