ID: 6571 | solute carrier family 18 member A2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (117241114..117279430) | PKDYS2, SVAT, SVMT, VAT2, VMAT2 | 193001 |
ID: 1312 | catechol-O-methyltransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19941772..19969975) | HEL-S-98n | 116790 |
ID: 1813 | dopamine receptor D2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (113409605..113475398, complement) | D2DR, D2R | 126450 |
ID: 338 | apolipoprotein B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (21001429..21044073, complement) | FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48 | 107730 |
ID: 6531 | solute carrier family 6 member 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (1392794..1445440, complement) | DAT, DAT1, PKDYS, PKDYS1 | 126455 |
ID: 105378500 | SLC18A2 antisense RNA 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (117238765..117241997, complement) | | |
ID: 4128 | monoamine oxidase A [Homo sapiens (human)] | Chromosome X, NC_000023.11 (43655006..43746817) | BRNRS, MAO-A | 309850 |
ID: 1457 | casein kinase 2 alpha 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (472498..543790, complement) | CK2A1, CKII, Cka1, Cka2, OCNDS | 115440 |
ID: 11315 | Parkinsonism associated deglycase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (7961711..7985505) | DJ-1, DJ1, GATD2, HEL-S-67p | 602533 |
ID: 1814 | dopamine receptor D3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (114127580..114199407, complement) | D3DR, ETM1, FET1 | 126451 |
ID: 3579 | C-X-C motif chemokine receptor 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (218125294..218137251) | CD182, CDw128b, CMKAR2, IL8R2, IL8RA, IL8RB, WHIMS2 | 146928 |
ID: 3716 | Janus kinase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (64833229..65067746, complement) | AIIDEA, JAK1B, JTK3, JAK1 | 147795 |
ID: 1812 | dopamine receptor D1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (175440036..175444182, complement) | D1R, DADRA, DRD1 | 126449 |
ID: 7054 | tyrosine hydroxylase [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (2163929..2171815, complement) | DYT14, DYT5b, TYH | 191290 |
ID: 2030 | solute carrier family 29 member 1 (Augustine blood group) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (44219615..44234142) | AUG, ENT1, hENT1 | 602193 |
ID: 7272 | TTK protein kinase [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (80004649..80042527) | CT96, ESK, MPH1, MPS1, MPS1L1, PYT | 604092 |
ID: 1459 | casein kinase 2 alpha 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (58157907..58198106, complement) | CK2A2, CK2alpha', CSNK2A1 | 115442 |
ID: 6041 | ribonuclease L [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (182573634..182589256, complement) | PRCA1, RNS4 | 180435 |
ID: 1452 | casein kinase 1 alpha 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (149492982..149551439, complement) | CK1, CK1a, CKIa, HEL-S-77p, HLCDGP1, PRO2975 | 600505 |
ID: 7026 | nuclear receptor subfamily 2 group F member 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (96326046..96340263) | ARP-1, ARP1, CHTD4, COUPTF2, COUPTFB, COUPTFII, NF-E3, SRXX5, SVP40, TFCOUP2 | 107773 |