ID: 7327 | ubiquitin conjugating enzyme E2 G2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44768580..44801820, complement) | UBC7 | 603124 |
ID: 7936 | negative elongation factor complex member E [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31952087..31958971, complement) | D6S45, NELF-E, RD, RDBP, RDP | 154040 |
ID: 27352 | small G protein signaling modulator 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (40370594..40410289) | CIP85, MAP, RABGAP5, RUSC3, RUTBC3, RabGAP-5, rabGAPLP | 610440 |
ID: 113402 | SFT2 domain containing 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (166319728..166342545, complement) | C6orf83, pRGR1 | |
ID: 55007 | family with sequence similarity 118 member A [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45308960..45341955) | C22orf8 | |
ID: 376497 | solute carrier family 27 member 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17468767..17506168) | ACSVL5, FATP, FATP-1, FATP1 | 600691 |
ID: 25829 | transmembrane protein 184B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (38216395..38273010, complement) | C22orf5, FM08, HS5O6A, HSPC256, SLC51C2 | |
ID: 3396 | mitochondrial ribosomal protein L58 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (75012670..75021261) | DS-1, DS1, ICT1, MRP-L58, mL62 | 603000 |
ID: 11190 | centrosomal protein 250 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (35455165..35519280) | C-NAP1, CEP2, CNAP1, CRDHL2 | 609689 |
ID: 8733 | glycosylphosphatidylinositol anchor attachment 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144082634..144086216) | GAA1, GPIBD15, hGAA1 | 603048 |
ID: 23288 | IQ motif containing E [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2558979..2614728) | 1700028P05Rik, PAPA7 | 617631 |
ID: 84971 | autophagy related 4D cysteine peptidase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10543904..10553418) | APG4-D, APG4D, AUTL4, HsAPG4D | 611340 |
ID: 93343 | multivesicular body subunit 12A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17405741..17425332) | CFBP, FAM125A | |
ID: 6687 | SPG7 matrix AAA peptidase subunit, paraplegin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89508388..89557768) | CAR, CMAR, PGN, SPG5C | 602783 |
ID: 51092 | SID1 transmembrane family member 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (117178743..117197442) | CGI-40 | 617551 |
ID: 6916 | thromboxane A synthase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (139778242..140020293) | BDPLT14, CYP5, CYP5A1, GHOSAL, THAS, TS, TXAS, TXS | 274180 |
ID: 8514 | potassium voltage-gated channel subfamily A regulatory beta subunit 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (5992676..6101180) | AKR6A5, HKvbeta2, HKvbeta2.1, HKvbeta2.2, KCNA2B, KV-BETA-2 | 601142 |
ID: 51720 | ubiquitin interaction motif containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176905005..177022602, complement) | RAP80, X2HRIP110 | 609433 |
ID: 396 | Rho GDP dissociation inhibitor alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81867721..81871337, complement) | GDIA1, HEL-S-47e, NPHS8, RHOGDI, RHOGDI-1 | 601925 |
ID: 27032 | ATPase secretory pathway Ca2+ transporting 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (130850595..131016712) | ATP2C1A, BCPM, HHD, PMR1, SPCA1, hSPCA1 | 604384 |