ID: 776 | calcium voltage-gated channel subunit alpha1 D [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (53494611..53813733) | CACH3, CACN4, CACNL1A2, CCHL1A2, Cav1.3, PASNA, SANDD | 114206 |
ID: 367 | androgen receptor [Homo sapiens (human)] | Chromosome X, NC_000023.11 (67544021..67730619) | AIS8, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM, AR | 313700 |
ID: 5071 | parkin RBR E3 ubiquitin protein ligase [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (161347417..162727766, complement) | AR-JP, LPRS2, PARK2, PDJ | 602544 |
ID: 2263 | fibroblast growth factor receptor 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (121478330..121598458, complement) | BBDS, BEK, BFR-1, CD332, CEK3, CFD1, ECT1, JWS, K-SAM, KGFR, TK14, TK25 | 176943 |
ID: 775 | calcium voltage-gated channel subunit alpha1 C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (1970780..2697950) | CACH2, CACN2-IT2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, NEDHLSS, TS, TS. LQT8, CACNA1C | 114205 |
ID: 1589 | cytochrome P450 family 21 subfamily A member 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32038415..32041644) | CA21H, CAH1, CPS1, CYP21, CYP21B, P450c21B | 613815 |
ID: 5478 | peptidylprolyl isomerase A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44796681..44803117) | CYPA, CYPH, HEL-S-69p | 123840 |
ID: 6262 | ryanodine receptor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (237042184..237833988) | ARVC2, ARVD2, RYR-2, RyR, VACRDS, VTSIP | 180902 |
ID: 476 | ATPase Na+/K+ transporting subunit alpha 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (116373244..116404774) | CMT2DD, HOMGSMR2 | 182310 |
ID: 3762 | potassium inwardly rectifying channel subfamily J member 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (128891356..128921163) | CIR, GIRK4, KATP1, KIR3.4, LQT13 | 600734 |
ID: 3783 | potassium calcium-activated channel subfamily N member 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (43766533..43780973, complement) | DHS2, IK, IK1, IKCA1, KCA4, KCa3.1, SK4, hIK1, hIKCa1, hKCa4, hSK4 | 602754 |
ID: 6804 | syntaxin 1A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (73699210..73719669, complement) | HPC-1, P35-1, STX1, SYN1A | 186590 |
ID: 6046 | bromodomain containing 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32968594..32981505) | BRD2-IT1, D6S113E, FSH, FSHRG1, FSRG1, NAT, O27.1.1, RING3, RNF3 | 601540 |
ID: 3745 | potassium voltage-gated channel subfamily B member 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49363877..49483362, complement) | DEE26, DRK1, Kv2.1 | 600397 |
ID: 53353 | LDL receptor related protein 1B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (140231423..142131016, complement) | LRP-1B, LRP-DIT, LRPDIT | 608766 |
ID: 793 | calbindin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (90058608..90082879, complement) | CALB, D-28K | 114050 |
ID: 9497 | solute carrier family 4 member 7 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (27372723..27484384, complement) | NBC2, NBC3, NBCN1, SBC2, SLC4A6 | 603353 |
ID: 25962 | vir like m6A methyltransferase associated [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94487689..94553469, complement) | KIAA1429, MSTP054, fSAP121 | 616447 |
ID: 23389 | mediator complex subunit 13L [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (115958576..116277693, complement) | MRFACD, PROSIT240, THRAP2, TRAP240L | 608771 |
ID: 57338 | junctophilin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (87601835..87698156) | CAGL237, HDL2, JP-3, JP3, TNRC22 | 605268 |