ID: 57719 | anoctamin 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17323223..17334855, complement) | KIAA1623, TMEM16H | 610216 |
ID: 63933 | mitochondrial calcium uniporter regulator 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (13786557..13814557, complement) | C6orf79, CCDC90A, FMP32 | 616952 |
ID: 84299 | migration and invasion enhancer 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39728510..39730532, complement) | C17orf37, C35, ORB3, RDX12, XTP4 | 611802 |
ID: 51006 | solute carrier family 35 member C2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46345984..46364425, complement) | BA394O2.1, C20orf5, CGI-15, OVCOV1 | 619530 |
ID: 200014 | coiled-coil and C2 domain containing 1B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (52350597..52366205, complement) | Lgd1 | |
ID: 23352 | ubiquitin protein ligase E3 component n-recognin 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (19074510..19210266, complement) | RBAF600, ZUBR1, p600 | 609890 |
ID: 339448 | chromosome 1 open reading frame 174 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (3889133..3900272, complement) | | |
ID: 9747 | TRPM8 channel associated factor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143851375..143902176, complement) | FAM115A, GATD9A | 616251 |
ID: 3998 | lectin, mannose binding 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (59327823..59359265, complement) | ERGIC-53, ERGIC53, F5F8D, FMFD1, MCFD1, MR60, gp58 | 601567 |
ID: 23303 | kinesin family member 13B [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (29067278..29263388, complement) | GAKIN | 607350 |
ID: 85015 | ubiquitin specific peptidase 45 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (99432325..99517846, complement) | LCA19 | 618439 |
ID: 51012 | PRELI domain containing 3B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (59033145..59042786, complement) | C20orf45, SLMO2, UPS2, dJ543J19.5 | 620754 |
ID: 55343 | solute carrier family 35 member C1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (45804072..45813016) | CDG2C, FUCT1 | 605881 |
ID: 79058 | ASPSCR1 tether for SLC2A4, UBX domain containing [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81977629..82017406) | ASPCR1, ASPL, ASPS, RCC17, TUG, UBXD9, UBXN9 | 606236 |
ID: 89781 | HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (26443109..26483863, complement) | BLOC3S2, LE | 606682 |
ID: 90007 | midnolin [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1248583..1259143) | Stx | 606700 |
ID: 113444 | small integral membrane protein 12 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (34850362..34859749, complement) | C1orf212 | |
ID: 64224 | HERPUD family member 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (35632659..35695135, complement) | | |
ID: 402055 | SRR1 domain containing [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (26483877..26494658) | HC/HCC, SRR1L | 602254 |
ID: 80772 | ceramide-1-phosphate transfer protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1324802..1328896) | GLTPD1 | 615467 |