ID: 6843 | vesicle associated membrane protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6462237..6470677, complement) | CMS25, SAX1, SPAX1, SYB1, VAMP-1 | 185880 |
ID: 79868 | ALG13 UDP-N-acetylglucosaminyltransferase subunit [Homo sapiens (human)] | Chromosome X, NC_000023.11 (111681170..111760649) | CDG1S, CXorf45, DEE36, EIEE36, GLT28D1, MDS031, TDRD13, YGL047W | 300776 |
ID: 285613 | RELT like 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (141636997..141641064) | C5orf16 | 611213 |
ID: 163050 | zinc finger protein 564 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12525373..12551482, complement) | | |
ID: 6605 | SWI/SNF related BAF chromatin remodeling complex subunit E1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40624962..40647818, complement) | BAF57, CSS5 | 603111 |
ID: 57187 | THO complex subunit 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (123600569..123733052, complement) | AMC7, CXorf3, MRX12, MRX35, THO2, XLID12, dJ506G2.1, hTREX120 | 300395 |
ID: 25923 | atlastin GTPase 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63624087..63671974, complement) | HSN1F | 609369 |
ID: 54819 | zinc finger CCHC-type containing 10 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132996985..133026549, complement) | | |
ID: 4839 | NOP2 nucleolar protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6556871..6568291, complement) | NOL1, NOP120, NSUN1, p120 | 164031 |
ID: 6170 | ribosomal protein L39 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (119786504..119791630, complement) | L39P42, RPL39_23_1806, eL39, RPL39 | 300899 |
ID: 80856 | lunapark, ER junction formation factor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (175923882..176002820, complement) | KIAA1715, LNP, LNP1, NEDEHCC, Ul, ulnaless | 610236 |
ID: 64417 | transmembrane protein 267 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (43444252..43484387, complement) | C5orf28 | |
ID: 3030 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26190635..26244632, complement) | ECHA, GBP, HADH, LCEH, LCHAD, MTPA, TP-ALPHA | 600890 |
ID: 51136 | ring finger protein, transmembrane 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (59952240..59964740, complement) | PTD016 | 615172 |
ID: 441150 | peroxisomal biogenesis factor 39 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (42890265..42890821, complement) | C6orf226 | |
ID: 5565 | protein kinase AMP-activated non-catalytic subunit beta 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (147155106..147172470, complement) | | 602741 |
ID: 7353 | ubiquitin recognition factor in ER associated degradation 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19449911..19479193, complement) | UFD1L | 601754 |
ID: 389119 | inka box actin regulator 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49803261..49805030) | C3orf54, FAM212A, INCA | 620426 |
ID: 3032 | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26244939..26290465) | ECHB, MSTP029, MTPB, MTPD, MTPD2, TP-BETA | 143450 |
ID: 56834 | G protein-coupled receptor 137 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64270531..64289500) | C11orf4A, TM7SF1L1, GPR137 | |