ID: 9997 | synthesis of cytochrome C oxidase 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (50523568..50526442, complement) | CEMCOX1, ECGF1, Gliostatin, MC4DN2, MYP6, PD-ECGF, SCO1L, TP, TYMP, TdRPase | 604272 |
ID: 4831 | NME/NM23 nucleoside diphosphate kinase 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (51165536..51171744) | NDKB, NDPK-B, NDPKB, NM23-H2, NM23B, PUF | 156491 |
ID: 80346 | receptor accessory protein 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22138020..22141907, complement) | C8orf20, PP432, Yip2c | 609349 |
ID: 9181 | Rho/Rac guanine nucleotide exchange factor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155946854..155979617, complement) | GEF, GEF-H1, GEFH1, LFP40, Lfc, NEDMHM, P40 | 607560 |
ID: 7335 | ubiquitin conjugating enzyme E2 V1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50081124..50115957, complement) | CIR1, CROC-1, CROC1, UBE2V, UEV-1, UEV1, UEV1A | 602995 |
ID: 64834 | ELOVL fatty acid elongase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43363401..43368011, complement) | CGI-88, IKSHD, Ssc1 | 611813 |
ID: 8079 | myeloid leukemia factor 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6747996..6753141, complement) | NTN4 | 601401 |
ID: 9813 | EF-hand calcium binding domain 14 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (46675159..46719114, complement) | KIAA0494 | 619559 |
ID: 2582 | UDP-galactose-4-epimerase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (23795599..23800754, complement) | SDR1E1, THC13 | 606953 |
ID: 83636 | chromosome 19 open reading frame 12 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29698886..29715789, complement) | MPAN, NBIA3, NBIA4, SPG43 | 614297 |
ID: 57657 | hyperpolarization activated cyclic nucleotide gated potassium channel 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155277463..155289848) | | 609973 |
ID: 3363 | 5-hydroxytryptamine receptor 7 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (90740823..90858039, complement) | 5-HT7 | 182137 |
ID: 201627 | DENN domain containing 6A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (57625454..57693077, complement) | AFI1A, FAM116A | 620561 |
ID: 51720 | ubiquitin interaction motif containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176905005..177022602, complement) | RAP80, X2HRIP110 | 609433 |
ID: 5478 | peptidylprolyl isomerase A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (44796681..44803117) | CYPA, CYPH, HEL-S-69p | 123840 |
ID: 84971 | autophagy related 4D cysteine peptidase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10543904..10553418) | APG4-D, APG4D, AUTL4, HsAPG4D | 611340 |
ID: 5338 | phospholipase D2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4807152..4823430) | PLD1C | 602384 |
ID: 25902 | methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (150865702..151101887) | FTHFSDC1, MTC1THFS, dJ292B18.2 | 611427 |
ID: 25829 | transmembrane protein 184B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38216395..38273010, complement) | C22orf5, FM08, HS5O6A, HSPC256, SLC51C2 | |
ID: 9690 | ubiquitin protein ligase E3C [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (157138926..157269370) | HECTH2, NDSMBA, NEDSMBA, RAUL | 614454 |