ID: 3755 | potassium voltage-gated channel modifier subfamily G member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (51003656..51023107, complement) | K13, KCNG, KV6.1, kH2 | 603788 |
ID: 6785 | ELOVL fatty acid elongase 4 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (79914814..79947553, complement) | ADMD, CT118, ISQMR, SCA34, STGD2, STGD3 | 605512 |
ID: 79905 | transmembrane channel like 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (18983934..19063942) | | 617198 |
ID: 57214 | cell migration inducing hyaluronidase 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (80779370..80951771) | CCSP11, HYBID, KIAA1199, TMEM2L, CEMIP | 608366 |
ID: 5333 | phospholipase C delta 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (38007496..38029642, complement) | NDNC3, PLC-III | 602142 |
ID: 27106 | arrestin domain containing 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18001124..18014102) | CLONE24945, PP2703 | |
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: 8974 | prolyl 4-hydroxylase subunit alpha 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132190147..132227853, complement) | MYP25, lncRNA-PE | 600608 |
ID: 84978 | FERM domain containing 5 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (43870764..44199473, complement) | NEDEMA | 616309 |
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: 54796 | basonuclin zinc finger protein 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (16409503..16870670, complement) | BSN2, LUTO, bn2 | 608669 |
ID: 3038 | hyaluronan synthase 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69083484..69118719) | | 602428 |
ID: 814 | calcium/calmodulin dependent protein kinase IV [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (111223583..111494886) | CaMK IV, CaMK-GR, CaMKIV, caMK | 114080 |
ID: 11247 | neurexophilin 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57216794..57226449) | NPH4 | 604637 |
ID: 7168 | tropomyosin 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (63042747..63071915) | C15orf13, CMD1Y, CMH3, HEL-S-265, HTM-alpha, LVNC9, TMSA | 191010 |
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: 130271 | pleckstrin homology, MyTH4 and FERM domain containing H2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (43637260..43767987) | PLEKHH1L | 612723 |
ID: 9569 | GTF2I repeat domain containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (74453906..74602605) | BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1 | 604318 |
ID: 6000 | regulator of G protein signaling 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (240774742..241357230, complement) | | 602517 |
ID: 114990 | vasorin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (4371848..4383538) | SLITL2 | 608843 |