| ID: 57153 | solute carrier family 44 member 2 (CTL2 blood group) [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10602455..10644557) | CTL2, PP1292 | 606106 |
| ID: 3958 | galectin 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (55129252..55145430) | CBP35, GAL3, GALBP, GALIG, L31, LGALS2, MAC2 | 153619 |
| ID: 7450 | von Willebrand factor [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (5948877..6124670, complement) | F8VWF, VWD | 613160 |
| ID: 3674 | integrin subunit alpha 2b [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44372181..44389649, complement) | BDPLT16, BDPLT2, CD41, CD41B, GP2B, GPIIb, GT, GT1, GTA, HPA3, PPP1R93 | 607759 |
| ID: 1991 | elastase, neutrophil expressed [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (852303..856243) | ELA2, GE, HLE, HNE, NE, PMN-E, SCN1 | 130130 |
| ID: 3965 | galectin 9 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (27631188..27649560) | HUATA, LGALS9 | 601879 |
| ID: 2648 | lysine acetyltransferase 2A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42113111..42121367, complement) | GCN5, GCN5L2, PCAF-b, hGCN5 | 602301 |
| ID: 3187 | heterogeneous nuclear ribonucleoprotein H1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179614178..179634784, complement) | HNRPH, HNRPH1, NEDCDS, hnRNPH | 601035 |
| ID: 623 | bradykinin receptor B1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96256210..96264763) | B1BKR, B1R, BKB1R, BKR1, BRADYB1 | 600337 |
| ID: 3357 | 5-hydroxytryptamine receptor 2B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (231108230..231125042, complement) | 5-HT(2B), 5-HT-2B, 5-HT2B | 601122 |
| ID: 6102 | RP2 activator of ARL3 GTPase [Homo sapiens (human)] | Chromosome X, NC_000023.11 (46837043..46882358) | DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2 | 300757 |
| ID: 26156 | ribosomal L1 domain containing 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (11833850..11851542, complement) | CSIG, L12, PBK1, UTP30 | 615874 |
| ID: 83639 | testis expressed 101 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (43388611..43418597) | CT131, GTPR867, NYD-SP8, PRO1884, SGRG, SPATA44, TES101RP | 612665 |
| ID: 23555 | tetraspanin 15 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (69451465..69549508) | 2700063A19Rik, NET-7, NET7, TM4SF15 | 613140 |
| ID: 440730 | tripartite motif containing 67 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231162058..231221565) | TNL | 610584 |
| ID: 84885 | zinc finger DHHC-type palmitoyltransferase 12 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128720873..128724127, complement) | DHHC-12, ZNF400 | |
| ID: 375057 | stum, mechanosensory transduction mediator homolog [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (226548764..226609230) | C1orf95 | |
| ID: 192343 | Record to support submission of GeneRIFs for a gene not in Gene (human). [Homo sapiens (human)] | | | |