| ID: 3785 | potassium voltage-gated channel subfamily Q member 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63400208..63472655, complement) | BFNC, DEE7, EBN, EBN1, ENB1, HNSPC, KCNA11, KV7.2 | 602235 |
| ID: 6667 | Sp1 transcription factor [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53380176..53416446) | | 189906 |
| ID: 185 | angiotensin II receptor type 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (148697903..148743003) | AG2SB, AT1, AT1AR, AT1B, AT1BR, AT1R, AT2R1, ATR1, HAT1R, AGTR1 | 106165 |
| ID: 5578 | protein kinase C alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66302613..66810743) | AAG6, PKC-alpha, PKCA, PKCI+/-, PKCalpha, PRKACA | 176960 |
| ID: 105372720 | KCNQ2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63448441..63449390) | | |
| ID: 4968 | 8-oxoguanine DNA glycosylase [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (9749952..9783108) | HMMH, HOGG1, MUTM, OGH1 | 601982 |
| ID: 3784 | potassium voltage-gated channel subfamily Q member 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2445008..2849105) | ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, RWS, SQT2, WRS | 607542 |
| ID: 6323 | sodium voltage-gated channel alpha subunit 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165984641..166149161, complement) | DEE6, DEE6A, DEE6B, DRVT, EIEE6, FEB3, FEB3A, FHM3, GEFSP2, HBSCI, NAC1, Nav1.1, SCN1, SMEI | 182389 |
| ID: 1457 | casein kinase 2 alpha 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (472498..543790, complement) | CK2A1, CKII, Cka1, Cka2, OCNDS | 115440 |
| ID: 801 | calmodulin 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90396502..90408268) | CALML2, CAM2, CAM3, CAMB, CAMC, CAMI, CAMIII, CPVT4, DD132, LQT14, PHKD, PHKD1, caM | 114180 |
| ID: 3786 | potassium voltage-gated channel subfamily Q member 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (132120861..132481095, complement) | BFNC2, EBN2, KV7.3 | 602232 |
| ID: 6925 | transcription factor 4 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (55222185..55635957, complement) | CDG2T, E2-2, FCD2, FECD3, ITF-2, ITF2, PTHS, SEF-2, SEF2, SEF2-1, SEF2-1A, SEF2-1B, SEF2-1D, TCF-4, bHLHb19 | 602272 |
| ID: 58 | actin alpha 1, skeletal muscle [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (229431245..229434094, complement) | ACTA, ASMA, CFTD, CFTD1, CFTDM, CMYO2A, CMYO2B, CMYO2C, CMYP2A, CMYP2B, CMYP2C, MPFD, NEM1, NEM2, NEM3, SHPM | 102610 |
| ID: 5978 | RE1 silencing transcription factor [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (56907900..56935844) | DFNA27, GINGF5, HGF5, NRSF, WT6, XBR | 600571 |
| ID: 6326 | sodium voltage-gated channel alpha subunit 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (165239414..165392304) | BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11, HBA, HBSCI, HBSCII, NAC2, Na(v)1.2, Nav1.21, SCN2A2, SCN2A | 182390 |
| ID: 7706 | tripartite motif containing 25 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56887909..56914049, complement) | EFP, RNF147, Z147, ZNF147 | 600453 |
| ID: 51280 | golgi membrane protein 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86026146..86100149, complement) | C9orf155, GOLPH2, GP73, HEL46, PSEC0257, bA379P1.3 | 606804 |
| ID: 7846 | tubulin alpha 1a [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49184795..49189080, complement) | B-ALPHA-1, LIS3, TUBA3 | 602529 |
| ID: 5034 | prolyl 4-hydroxylase subunit beta [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81843166..81860535, complement) | CLCRP1, DSI, ERBA2L, GIT, P4Hbeta, PDI, PDIA1, PHDB, PO4DB, PO4HB, PROHB | 176790 |
| ID: 808 | calmodulin 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (46601074..46610782) | CALM, CAM1, CAM2, CAMB, CPVT6, CaM, CaMIII, HEL-S-72, LQT16, PHKD, PHKD3 | 114183 |