ID: 10052 | gap junction protein gamma 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44794104..44831364, complement) | CX45, GJA7 | 608655 |
ID: 7424 | vascular endothelial growth factor C [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (176683538..176792922, complement) | Flt4-L, LMPH1D, LMPHM4, VRP | 601528 |
ID: 2972 | BRF1 RNA polymerase III transcription initiation factor subunit [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (105209286..105315589, complement) | BRF, BRF-1, CFDS, GTF3B, HEL-S-76p, TAF3B2, TAF3C, TAFIII90, TF3B90, TFIIIB90, hBRF | 604902 |
ID: 5333 | phospholipase C delta 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (38007496..38029642, complement) | NDNC3, PLC-III | 602142 |
ID: 79567 | RHO family interacting cell polarization regulator 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (67518369..67546786) | FAM65A | 619842 |
ID: 23251 | membrane integral NOTCH2 associated receptor 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (79411400..79472304) | KIAA1024, UBTOR | 618054 |
ID: 6567 | solute carrier family 16 member 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (74421493..74533916) | AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT | 300095 |
ID: 332 | baculoviral IAP repeat containing 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78214253..78225635) | API4, EPR-1 | 603352 |
ID: 6553 | solute carrier family 9 member A5 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (67248979..67272191) | NHE5 | 600477 |
ID: 50863 | neurotrimin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (131370615..132336822) | CEPU-1, HNT, IGLON2, NTRI | 607938 |
ID: 57449 | pleckstrin homology and RhoGEF domain containing G5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6467122..6520092, complement) | ARHGEF45, CMTRIC, DSMA4, GEF720, HMNR4, Syx, Tech | 611101 |
ID: 54620 | F-box and leucine rich repeat protein 19 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30922851..30948783) | CXXC11, Fbl19, JHDM1C | 609085 |
ID: 55068 | ecto-NOX disulfide-thiol exchanger 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (43213130..43786972, complement) | CNOX, PIG38, bA64J21.1, cCNOX | 610914 |
ID: 55721 | IQ motif containing C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32205671..32208682) | | |
ID: 4237 | microfibril associated protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16974502..16981583, complement) | MAGP, MAGP-1, MAGP1 | 156790 |
ID: 54796 | basonuclin zinc finger protein 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16409503..16870670, complement) | BSN2, LUTO, bn2 | 608669 |