ID: 4124 | mannosidase alpha class 2A member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (109689927..109869625) | AMan II, GOLIM7, MANA2, MANII | 154582 |
ID: 1739 | discs large MAGUK scaffold protein 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (197042560..197299321, complement) | DLGH1, SAP-97, SAP97, hdlg | 601014 |
ID: 2720 | galactosidase beta 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (32961108..33097146, complement) | EBP, ELNR1, MPS4B | 611458 |
ID: 643853 | transmembrane protein with metallophosphoesterase domain [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (33090422..33097146, complement) | | |
ID: 6738 | Ro60, Y RNA binding protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (193059612..193091777) | RORNP, SSA2, TROVE2 | 600063 |
ID: 3685 | integrin subunit alpha V [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (186590056..186680901) | CD51, MSK8, VNRA, VTNR | 193210 |
ID: 51374 | all-trans retinoic acid induced differentiation factor [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27212041..27217183) | APR--3, APR-3, APR3, C2orf28, HSPC013, PRO240, p18 | 619682 |
ID: 23597 | acyl-CoA thioesterase 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23701055..23743276, complement) | ACATE2, CGI-16, MT-ACT48, MTACT48 | 300862 |
ID: 64969 | mitochondrial ribosomal protein S5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (95085369..95122003, complement) | MRP-S5, S5mt, uS5m | 611972 |
ID: 7323 | ubiquitin conjugating enzyme E2 D3 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (102794383..102868895, complement) | E2(17)KB3, UBC4/5, UBCH5C | 602963 |
ID: 65062 | transmembrane protein 237 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (201620186..201643503, complement) | ALS2CR4, JBTS14 | 614423 |
ID: 28966 | sorting nexin 24 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (122845613..123029318) | PRO1284, SBBI31 | |
ID: 6526 | solute carrier family 5 member 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34073578..34106260) | BCW2, SMIT, SMIT1, SMIT2 | 600444 |
ID: 64844 | membrane associated ring-CH-type finger 7 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (159712506..159771027) | AXO, AXOT, MARCH-VII, MARCH7, RNF177 | 613334 |
ID: 8884 | solute carrier family 5 member 6 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27199587..27212787, complement) | COMNB, NERIB, SMVT, SMVTD, hSMVT | 604024 |
ID: 64769 | MYST/Esa1 associated factor 6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37489993..37514766, complement) | C1orf149, CENP-28, EAF6, NY-SAR-91 | 611001 |
ID: 10114 | homeodomain interacting protein kinase 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (33256672..33357023) | DYRK6, FIST3, PKY, YAK1 | 604424 |
ID: 53407 | syntaxin 18 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (4418968..4542343, complement) | Ufe1 | 606046 |
ID: 339448 | chromosome 1 open reading frame 174 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (3889133..3900272, complement) | | |
ID: 10766 | transducer of ERBB2, 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41433494..41446801, complement) | APRO5, TOB4, TOBL, TROB2 | 607396 |