ID: 7173 | thyroid peroxidase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (1374047..1543673) | MSA, TDH2A, TPX | 606765 |
ID: 6396 | SEC13 homolog, nuclear pore and COPII coat complex component [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (10300931..10321112, complement) | D3S1231EL1, SEC13R, npp-20, SEC13 | 600152 |
ID: 6456 | SH3 domain containing GRB2 like 2, endophilin A1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (17579066..17797124) | CNSA2, EEN-B1, SH3D2A, SH3P4 | 604465 |
ID: 6519 | solute carrier family 3 member 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (44275480..44322437) | ATR1, CSNU1, D2H, NBAT, RBAT | 104614 |
ID: 6543 | solute carrier family 8 member A2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47428017..47471893, complement) | NCX2 | 601901 |
ID: 6699 | small proline rich protein 1B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (153031203..153032900) | CORNIFIN, GADD33, SPR-IB, SPRR1 | 182266 |
ID: 6742 | single stranded DNA binding protein 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (141738321..141750488) | Mt-SSB, OPA13, SOSS-B1, SSBP, mtSSB | 600439 |
ID: 6988 | T cell leukemia translocation altered [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49412423..49416476) | | 600690 |
ID: 7054 | tyrosine hydroxylase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2163929..2171815, complement) | DYT14, DYT5b, TYH | 191290 |
ID: 6376 | C-X3-C motif chemokine ligand 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (57372490..57385044) | ABCD-3, C3Xkine, CXC3, CXC3C, NTN, NTT, SCYD1, fractalkine, neurotactin | 601880 |
ID: 7252 | thyroid stimulating hormone subunit beta [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (115029826..115034309) | TSH-B, TSH-BETA | 188540 |
ID: 7320 | ubiquitin conjugating enzyme E2 B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (134371569..134392108) | E2-17kDa, HHR6B, HR6B, RAD6B, UBC2 | 179095 |
ID: 7398 | ubiquitin specific peptidase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (62436395..62451804) | UBP | 603478 |
ID: 7472 | Wnt family member 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (117275451..117323058, complement) | INT1L1, IRP | 147870 |
ID: 7536 | splicing factor 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64764606..64778542, complement) | BBP, D11S636, MBBP, ZCCHC25, ZFM1, ZNF162 | 601516 |
ID: 7626 | zinc finger protein 75D [Homo sapiens (human)] | Chromosome X, NC_000023.11 (135248589..135344109, complement) | D8C6, ZKSCAN24, ZNF75, ZNF82, ZSCAN28 | 314997 |
ID: 7644 | zinc finger protein 91 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (23305004..23395471, complement) | HPF7, HTF10 | 603971 |
ID: 5747 | protein tyrosine kinase 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (140657900..141002079, complement) | FADK, FADK 1, FAK, FAK1, FRNK, PPP1R71, p125FAK, pp125FAK | 600758 |
ID: 5313 | pyruvate kinase L/R [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155289293..155308654, complement) | CNSHA2, PK1, PKL, PKRL, RPK | 609712 |
ID: 5317 | plakophilin 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201283506..201332989) | B6P, EDSFS | 601975 |