ID: 112495 | general transcription factor IIIC subunit 6 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (110958706..110967872) | C6orf51, TFIIIC35, bA397G5.3 | 611784 |
ID: 351 | amyloid beta precursor protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25880550..26171128, complement) | AAA, ABETA, ABPP, AD1I, CTFgamma, CVAP, PN-II, PN2, alpha-sAPP, preA4, APP | 104760 |
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: 960 | CD44 molecule (IN blood group) [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (35139171..35232402) | CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL, HUTCH-1, HUTCH-I, Hermes-1, IN, LHR, MC56, MDU2, MDU3, MIC4, Pgp1 | 107269 |
ID: 2146 | enhancer of zeste 2 polycomb repressive complex 2 subunit [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (148807383..148884291, complement) | ENX-1, ENX1b, KMT6, KMT6A, WVS, WVS2, EZH2 | 601573 |
ID: 3075 | complement factor H [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (196652043..196747504) | AHUS1, AMBP1, ARMD4, ARMS1L3, FH, FHL1, HF, HF1, HF2, HUS, CFH | 134370 |
ID: 100129001 | GTF3C6 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (95584238..95585030) | | |
ID: 646745 | GTF3C6 pseudogene 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (29551510..29552224) | | |
ID: 644563 | GTF3C6 pseudogene 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (107131578..107132351) | | |
ID: 4087 | SMAD family member 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (47808957..47930872, complement) | CHTD8, JV18, JV18-1, LDS6, MADH2, MADR2, hMAD-2, hSMAD2 | 601366 |
ID: 23476 | bromodomain containing 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (15235519..15332539, complement) | CAP, CDLS6, FSHRG4, HUNK1, HUNKI, MCAP | 608749 |
ID: 8452 | cullin 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (224470150..224585363, complement) | CUL-3, NEDAUS, PHA2E | 603136 |
ID: 10482 | nuclear RNA export factor 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62792130..62805440, complement) | MEX67, TAP | 602647 |
ID: 2962 | general transcription factor IIF subunit 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (6379572..6393164, complement) | BTF4, RAP74, TF2F1, TFIIF | 189968 |
ID: 6138 | ribosomal protein L15 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (23916545..23924631) | DBA12, EC45, L15, RPL10, RPLY10, RPYL10, eL15 | 604174 |
ID: 10212 | DExD-box helicase 39A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (14408798..14419383, complement) | BAT1, BAT1L, DDX39, DDXL, URH49 | 619906 |
ID: 23524 | serine/arginine repetitive matrix 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2752638..2771412) | 300-KD, CWF21, Cwc21, HSPC075, MRD72, SRL300, SRm300 | 606032 |
ID: 2975 | general transcription factor IIIC subunit 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (27460613..27549913, complement) | TFIIIC, TFIIIC220, TFIIICalpha | 603246 |
ID: 53981 | cleavage and polyadenylation specific factor 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92121969..92172145) | CPSF100 | 606028 |
ID: 79155 | TNFAIP3 interacting protein 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (2741648..2756336, complement) | ABIN2, FLIP1, KLIP | 610669 |