| ID: 100529226 | Chromosome 17q21.31 duplication syndrome [Homo sapiens (human)] | | C17DUPq21.31 | 613533 |
| ID: 4137 | microtubule associated protein tau [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45894554..46028334) | DDPAC, FTD1, FTDP-17L, MSTD, MTBT1, MTBT2, PPND, PPP1R103, TAU, Tau-PHF6, tau-40, MAPT | 157140 |
| ID: 3881 | keratin 31 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41393721..41397608, complement) | HA1, Ha-1, KRTHA1, hHa1 | 601077 |
| ID: 125111 | gap junction protein delta 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40360652..40364737, complement) | CX31.9, Cx30.2, GJA11, GJC1 | 607425 |
| ID: 284064 | ribosomal protein L29 pseudogene 31 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43476154..43476765) | PERMIT, RPL29_11_1549, p17 | |
| ID: 284058 | KAT8 regulatory NSL complex subunit 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (46029916..46225367, complement) | C17DELq21.31, CENP-36, DEL17Q21.31, KDVS, KIAA1267, MSL1v1, NSL1, hMSL1v1 | 612452 |
| ID: 2896 | granulin precursor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44345302..44353106) | CLN11, FTD2, GEP, GP88, PCDGF, PEPI, PGRN | 138945 |
| ID: 1394 | corticotropin releasing hormone receptor 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45784320..45835828) | CRF-R, CRF-R-1, CRF-R1, CRF1, CRFR-1, CRFR1, CRH-R-1, CRH-R1, CRHRL, CRHR1 | 122561 |
| ID: 6622 | synuclein alpha [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (89724099..89838304, complement) | NACP, PARK1, PARK4, PD1 | 163890 |
| ID: 9839 | zinc finger E-box binding homeobox 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (144384081..144520119, complement) | HSPC082, SIP-1, SIP1, SMADIP1, ZFHX1B | 605802 |
| ID: 246744 | saitohin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45999250..45999694) | MAPTIT | 607067 |
| ID: 672 | BRCA1 DNA repair associated [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43044295..43170327, complement) | BRCAI, BRCC1, BROVCA1, FANCS, IRIS, PNCA4, PPP1R53, PSCP, RNF53 | 113705 |
| ID: 2064 | erb-b2 receptor tyrosine kinase 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39688094..39728658) | CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19, NEU, NGL, TKR1, VSCN2, c-ERB-2, c-ERB2, p185(erbB2) | 164870 |
| ID: 201176 | Rho GTPase activating protein 27 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45393908..45432870, complement) | CAMGAP1, PP905, SH3D20, SH3P20 | 610591 |
| ID: 9343 | elongation factor Tu GTP binding domain containing 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44849948..44899445, complement) | MFDGA, MFDM, SNRNP116, Snrp116, Snu114, U5-116KD | 603892 |
| ID: 80174 | DBF4B-CDC7 kinase regulatory subunit [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44708665..44752264) | ASKL1, CHIFB, DRF1, ZDBF1B | 611661 |
| ID: 8913 | calcium voltage-gated channel subunit alpha1 G [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50560715..50627474) | Ca(V)T.1, Cav3.1, NBR13, SCA42, SCA42ND | 604065 |
| ID: 535 | ATPase H+ transporting V0 subunit a1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42458878..42522579) | ATP6N1, ATP6N1A, DEE104, NEDEBA, Stv1, VPP1, Vph1, a1 | 192130 |
| ID: 8678 | beclin 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42810132..42824282, complement) | ATG6, VPS30, beclin1 | 604378 |
| ID: 6521 | solute carrier family 4 member 1 (Diego blood group) [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44248390..44268135, complement) | AE1, BND3, CD233, CHC, DI, EMPB3, EPB3, FR, RTA1A, SAO, SPH4, SW, WD, WD1, WR | 109270 |