ID: 4641 | myosin IC [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1464186..1492686, complement) | MMI-beta, MMIb, MyoIC, NMI, myr2 | 606538 |
ID: 8683 | serine and arginine rich splicing factor 9 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120461672..120469748, complement) | SFRS9, SRp30c | 601943 |
ID: 1039 | cerebellar degeneration related protein 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (22345936..22374619, complement) | CDR62, Yo | 117340 |
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: 91 | activin A receptor type 1B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51951699..51997078) | ACTRIB, ACVRLK4, ALK4, SKR2 | 601300 |
ID: 7263 | thiosulfate sulfurtransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37010859..37020183, complement) | RDS | 180370 |
ID: 84262 | proteasome assembly chaperone 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (1567332..1570032, complement) | C7orf48, PAC3 | 617528 |
ID: 488 | ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (110280616..110351093) | ATP2B, DAR, DD, SERCA2 | 108740 |
ID: 5829 | paxillin [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120210447..120265730, complement) | | 602505 |
ID: 6923 | elongin B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2771414..2777280, complement) | SIII, TCEB2 | 600787 |
ID: 10019 | SH2B adaptor protein 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (111404730..111451623) | IDDM20, LNK | 605093 |
ID: 399665 | estrogen-induced osteoclastogenesis regulator 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127940582..127980989, complement) | C9orf132, FAM102A, SYM-3A, bA203J24.7 | 610891 |
ID: 123803 | N-terminal asparagine amidase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15037857..15056074, complement) | PNAA, PNAD | 615367 |
ID: 4814 | ninjurin 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (93121496..93134251, complement) | NIN1, NINJURIN, hNINJ1 | 602062 |
ID: 55615 | proline rich 5 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (44668751..44737681) | FLJ20185k, PP610, PROTOR-1, PROTOR1 | 609406 |
ID: 4357 | mercaptopyruvate sulfurtransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37019742..37029815) | MST, TST2, TUM1 | 602496 |
ID: 23039 | exportin 7 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (21919662..22006585) | EXP7, RANBP16 | 606140 |
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: 734 | oxidative stress induced growth inhibitor family member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (89901868..89927888) | C8orf1, hT41 | 604598 |
ID: 9057 | solute carrier family 7 member 6 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68264526..68301819) | LAT-2, LAT3, y+LAT-2 | 605641 |