ID: 9416 | DEAD-box helicase 23 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48829756..48852163, complement) | PRPF28, SNRNP100, U5-100K, U5-100KD, prp28 | 612172 |
ID: 283951 | ubiquinol-cytochrome c reductase complex assembly factor 4 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1419752..1420747, complement) | C16orf91, CCSMST1, URLC5, gs103 | 620578 |
ID: 54925 | zinc finger and SCAN domain containing 32 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3382085..3401004, complement) | HCCS-5, ZNF434 | |
ID: 7126 | TNF alpha induced protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28335761..28347009) | B12, B61, BTBD34, EDP1, hBACURD2 | 191161 |
ID: 30851 | Tax1 binding protein 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (3662895..3668578, complement) | TIP-1, TIP1 | 616484 |
ID: 90410 | intraflagellar transport 20 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28328326..28335472, complement) | | 614394 |
ID: 5529 | protein phosphatase 2 regulatory subunit B'epsilon [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (63371364..63543377, complement) | B56E, B56epsilon | 601647 |
ID: 23019 | CCR4-NOT transcription complex subunit 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (58519951..58629826, complement) | AD-005, CDC39, HPE12, NOT1, NOT1H, VIBOS | 604917 |
ID: 80765 | StAR related lipid transfer domain containing 5 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (81309053..81324141, complement) | | 607050 |
ID: 84933 | chromosome 8 open reading frame 76 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (123219967..123241377, complement) | | |
ID: 51573 | glycerophosphodiester phosphodiesterase 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (19501693..19522098, complement) | 363E6.2, MIR16 | 605943 |
ID: 57062 | DEAD-box helicase 24 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (94048287..94081202, complement) | | 606181 |
ID: 56262 | leucine rich repeat containing 8 VRAC subunit A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128882133..128918039) | AGM5, HsLRRC8A, LRRC8, SWELL1 | 608360 |
ID: 58485 | trafficking protein particle complex subunit 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7930345..7931999, complement) | BET5, MUM2 | 610969 |
ID: 10940 | POP1 homolog, ribonuclease P/MRP subunit [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98117293..98159835) | ANXD2 | 602486 |
ID: 84464 | SLX4 structure-specific endonuclease subunit [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3581181..3611606, complement) | BTBD12, FANCP, MUS312 | 613278 |
ID: 85365 | ALG2 alpha-1,3/1,6-mannosyltransferase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (99216425..99221942, complement) | CDG1I, CDGIi, CMS14, CMSTA3, NET38, hALPG2 | 607905 |
ID: 60528 | elaC ribonuclease Z 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (12991612..13018027, complement) | COXPD17, ELC2, HPC2 | 605367 |
ID: 80314 | enhancer of polycomb homolog 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (32267751..32378769, complement) | Epl1 | 610999 |
ID: 4285 | mitochondrial intermediate peptidase [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (23730189..23889400, complement) | COXPD31, HMIP, MIP | 602241 |