ID: 51016 | ER membrane protein complex subunit 9 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (24138965..24141591, complement) | C14orf122, CGI-112, FAM158A | |
ID: 374659 | HD domain containing 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90929968..90932569, complement) | (ppGpp)ase, MESH1, MYNRL15 | |
ID: 84464 | SLX4 structure-specific endonuclease subunit [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3581181..3611606, complement) | BTBD12, FANCP, MUS312 | 613278 |
ID: 22845 | dolichol kinase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128945530..128947603, complement) | CDG1M, DK, DK1, SEC59, TMEM15 | 610746 |
ID: 23511 | nucleoporin 188 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128947699..129007096) | KIAA0169, SANDSTEF, hNup188 | 615587 |
ID: 9252 | ribosomal protein S6 kinase A5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90847861..91060641, complement) | MSK1, MSPK1, RLPK | 603607 |
ID: 8509 | N-deacetylase and N-sulfotransferase 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (73801916..73811820, complement) | HSST2, N-HSST 2, NST2 | 603268 |
ID: 2037 | erythrocyte membrane protein band 4.1 like 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (130839347..131063245, complement) | 4.1-G, 4.1G | 603237 |
ID: 55102 | autophagy related 2B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96279195..96363341, complement) | BLTP4B, C14orf103 | 616226 |
ID: 51659 | GINS complex subunit 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (85676198..85688954, complement) | HSPC037, PSF2, Pfs2 | 610609 |
ID: 121268 | RHEB like 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49064676..49069979, complement) | RHEBL1c | 618956 |
ID: 112950 | mediator complex subunit 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43383917..43389800, complement) | ARC32 | 607956 |
ID: 2975 | general transcription factor IIIC subunit 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (27460613..27549913, complement) | TFIIIC, TFIIIC220, TFIIICalpha | 603246 |
ID: 29959 | nuclear receptor binding protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27427790..27442259) | BCON3, MADM, MUDPNP, NRBP | 606010 |
ID: 84138 | solute carrier family 7 member 6 opposite strand [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68298034..68310946, complement) | EPM12, Iwr1 | 619192 |
ID: 55177 | regulator of microtubule dynamics 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40735887..40755254, complement) | FAM82A2, FAM82C, RMD-3, RMD3, ptpip51 | 611873 |
ID: 54496 | protein arginine methyltransferase 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68311019..68360870) | SBIDDS | 610087 |
ID: 8727 | catenin alpha like 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (108942577..109013499, complement) | ACRP, CLLP, alpha-CATU | 604785 |
ID: 784 | calcium voltage-gated channel auxiliary subunit beta 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48814480..48828941) | CAB3, CACNLB3 | 601958 |
ID: 2665 | GDP dissociation inhibitor 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (5765223..5813434, complement) | HEL-S-46e, RABGDIB | 600767 |