ID: 6263 | ryanodine receptor 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (33310967..33866102) | CMYO20, CMYP20, RYR-3 | 180903 |
ID: 5728 | phosphatase and tensin homolog [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (87863625..87971930) | 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC11, PTENbeta, PTENgama, TEP1, PTEN | 601728 |
ID: 1080 | CF transmembrane conductance regulator [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117480025..117668665) | ABC35, ABCC7, CF/MRP, MRP7, TNR-CFTR, dJ760C5.1, CFTR | 602421 |
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: 101928134 | RYR3 divergent transcript [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (33303657..33310659, complement) | | |
ID: 598 | BCL2 like 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (31664452..31723963, complement) | BCL-XL/S, BCL2L, BCLX, Bcl-X, PPP1R52 | 600039 |
ID: 6261 | ryanodine receptor 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38433691..38587564) | CCO, CMYO1A, CMYO1B, CMYP1A, CMYP1B, KDS, MHS, MHS1, PPP1R137, RYDR, RYR, RYR-1, SKRR | 180901 |
ID: 648 | BMI1 proto-oncogene, polycomb ring finger [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (22321099..22331706) | FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1 | 164831 |
ID: 6927 | HNF1 homeobox A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120978543..121002512) | HNF-1-alpha, HNF-1A, HNF1, HNF1alpha, HNF4A, IDDM20, LFB1, MODY3, TCF-1, TCF1 | 142410 |
ID: 6262 | ryanodine receptor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (237042184..237833988) | ARVC2, ARVD2, RYR-2, RyR, VACRDS, VTSIP | 180902 |
ID: 7415 | valosin containing protein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35056064..35072625, complement) | CDC48, FTDALS6, TERA, p97 | 601023 |
ID: 3329 | heat shock protein family D (Hsp60) member 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (197486584..197500274, complement) | CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13 | 118190 |
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: 8454 | cullin 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (148697756..148801110) | | 603134 |
ID: 2023 | enolase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (8861000..8878686, complement) | ENO1-IT1L1, HEL-S-17, MPB1, NNE, PPH, ENO1 | 172430 |
ID: 1832 | desmoplakin [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (7541671..7586714) | DCWHKTA, DP | 125647 |
ID: 3708 | inositol 1,4,5-trisphosphate receptor type 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (4493348..4847506) | ACV, CLA4, INSP3R1, IP3R, IP3R1, PPP1R94, SCA15, SCA16, SCA29 | 147265 |
ID: 57142 | reticulon 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (54972189..55137831, complement) | ASY, NI220/250, NOGO, NSP, NSP-CL, Nbla00271, Nbla10545, RTN-X-A, RTN4-B1, RTN4-B2, RTN4-C, RTN4 | 604475 |
ID: 2280 | FKBP prolyl isomerase 1A [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (1368978..1393054, complement) | FKBP-12, FKBP-1A, FKBP1, FKBP12, PKC12, PKCI2, PPIASE | 186945 |
ID: 7074 | TIAM Rac1 associated GEF 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (31118418..31559087, complement) | NEDLDS, TIAM-1 | 600687 |