ID: 113829 | solute carrier family 35 member A4 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (140564828..140569100) | | 620297 |
ID: 1312 | catechol-O-methyltransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19941772..19969975) | HEL-S-98n | 116790 |
ID: 4000 | lamin A/C [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156082573..156140081) | CDCD1, CDDC, CMD1A, CMT2B1, EMD2, FPL, FPLD, FPLD2, HGPS, IDC, LDP1, LFP, LGMD1B, LMN1, LMNC, LMNL1, MADA, PRO1 | 150330 |
ID: 124900836 | SLC35A4 upstream open reading frame protein-like [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (71301265..71301934, complement) | | |
ID: 107986208 | probable UDP-sugar transporter protein SLC35A4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (71300257..71301179, complement) | | |
ID: 624 | bradykinin receptor B2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96204839..96244164) | B2R, BK-2, BK2, BKR2, BRB2 | 113503 |
ID: 7706 | tripartite motif containing 25 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56887909..56914049, complement) | EFP, RNF147, Z147, ZNF147 | 600453 |
ID: 3191 | heterogeneous nuclear ribonucleoprotein L [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38836370..38852347, complement) | HNRPL, P/OKcl.14, hnRNP-L | 603083 |
ID: 6923 | elongin B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2771414..2777280, complement) | SIII, TCEB2 | 600787 |
ID: 2703 | gap junction protein alpha 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (147902795..147914486) | CAE, CAE1, CTRCT1, CX50, CZP1, MP70 | 600897 |
ID: 9166 | estrogen receptor binding site associated antigen 9 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (109539702..109565996) | EB9, PDAF | 605772 |
ID: 1727 | cytochrome b5 reductase 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (42617840..42649392, complement) | B5R, DIA1 | 613213 |
ID: 8519 | interferon induced transmembrane protein 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (314040..315272) | 9-27, CD225, DSPA2a, IFI17, LEU13 | 604456 |
ID: 4343 | Mov10 RNA helicase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (112674439..112700739) | fSAP113, gb110 | 610742 |
ID: 90993 | cAMP responsive element binding protein 3 like 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (46277662..46321409) | C16DELp11.2, DEL16p11.2, OASIS, OI16 | 616215 |
ID: 127833 | synaptotagmin 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202590596..202710454, complement) | CMS7, CMS7A, CMS7B, MYSPC, SytII | 600104 |
ID: 55800 | sodium voltage-gated channel beta subunit 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (123629188..123654624, complement) | ATFB16, BRGDA7, HSA243396, SCNB3 | 608214 |
ID: 51614 | ERGIC and golgi 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (35542078..35557634) | C20orf47, C2orf47, CGI-54, Erv46, NY-BR-84, PRO0989, SDBCAG84, dJ477O4.2 | 616971 |
ID: 2686 | gamma-glutamyltransferase 7 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (34844720..34872856, complement) | D20S101, GGT4, GGTL3, GGTL5 | 612342 |
ID: 65062 | transmembrane protein 237 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (201620186..201643503, complement) | ALS2CR4, JBTS14 | 614423 |