ID: 343099 | coiled-coil domain containing 18 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (93179913..93278730) | NY-SAR-41 | |
ID: 1312 | catechol-O-methyltransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19941772..19969975) | HEL-S-98n | 116790 |
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: 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: 100131564 | CCDC18 antisense RNA 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (93310109..93345811, complement) | | |
ID: 7430 | ezrin [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (158765748..158819368, complement) | CVIL, CVL, HEL-S-105, VIL2 | 123900 |
ID: 1051 | CCAAT enhancer binding protein beta [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50190583..50192690) | C/EBP-beta, IL6DBP, NF-IL6, TCF5 | 189965 |
ID: 7534 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (100916523..100953382, complement) | 14-3-3-zeta, HEL-S-3, HEL-S-93, HEL4, KCIP-1, POPCHAS, YWHAD | 601288 |
ID: 3880 | keratin 19 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41523617..41528308, complement) | CK19, K19, K1CS | 148020 |
ID: 3875 | keratin 18 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (52948855..52952906) | CK-18, CYK18, K18 | 148070 |
ID: 5829 | paxillin [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120210447..120265730, complement) | | 602505 |
ID: 7531 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (1344275..1400222, complement) | 14-3-3E, HEL2, KCIP-1, MDCR, MDS | 605066 |
ID: 10971 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (9583967..9630997, complement) | 14-3-3, 1C5, HS1 | 609009 |
ID: 2810 | stratifin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (26863149..26864456) | YWHAS | 601290 |
ID: 7529 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein beta [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (44885705..44908532) | GW128, HEL-S-1, HS1, KCIP-1, YWHAA | 601289 |
ID: 3856 | keratin 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (52897191..52949860, complement) | CARD2, CK-8, CK8, CYK8, K2C8, K8, KO | 148060 |
ID: 7532 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76326799..76358991, complement) | 14-3-3GAMMA, DEE56, EIEE56, PPP1R170 | 605356 |
ID: 9113 | large tumor suppressor kinase 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (149658153..149718101, complement) | WARTS, wts | 603473 |
ID: 7533 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (31944535..31957603) | YWHA1 | 113508 |
ID: 506 | ATP synthase F1 subunit beta [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56638175..56645984, complement) | ATP5B, ATPMB, ATPSB, HEL-S-271, HUMOP2 | 102910 |