ID: 92745 | solute carrier family 38 member 5 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48458544..48470260, complement) | JM24, SN2, SNAT5, pp7194 | 300649 |
ID: 3106 | major histocompatibility complex, class I, B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31353875..31357179, complement) | AS, B-4901, HLAB | 142830 |
ID: 3958 | galectin 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (55129252..55145430) | CBP35, GAL3, GALBP, GALIG, L31, LGALS2, MAC2 | 153619 |
ID: 5879 | Rac family small GTPase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (6374527..6403967) | MIG5, MRD48, Rac-1, TC-25, p21-Rac1 | 602048 |
ID: 387 | ras homolog family member A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49359145..49411976, complement) | ARH12, ARHA, EDFAOB, RHO12, RHOH12 | 165390 |
ID: 19 | ATP binding cassette subfamily A member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (104781006..104928155, complement) | ABC-1, ABC1, CERP, HDLCQTL13, HDLDT1, HPALP1, TGD | 600046 |
ID: 7316 | ubiquitin C [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (124911646..124914650, complement) | HMG20 | 191340 |
ID: 3965 | galectin 9 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (27631188..27649560) | HUATA, LGALS9 | 601879 |
ID: 5573 | protein kinase cAMP-dependent type I regulatory subunit alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (68413623..68551316) | ACRDYS1, ADOHR, CAR, CNC, CNC1, PKR1, PPNAD1, PRKAR1, Prkar1alpha, TSE1 | 188830 |
ID: 388 | ras homolog family member B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (20447074..20449440) | ARH6, ARHB, MST081, MSTP081, RHOH6 | 165370 |
ID: 939 | CD27 molecule [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6443892..6451713) | S152, S152. LPFS2, T14, TNFRSF7, Tp55 | 186711 |
ID: 3820 | killer cell lectin like receptor B1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (9594551..9607916, complement) | CD161, CLEC5B, NKR, NKR-P1, NKR-P1A, NKRP1A, hNKR-P1A | 602890 |
ID: 8794 | TNF receptor superfamily member 10c [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23102921..23117445) | CD263, DCR1, DCR1-TNFR, LIT, TRAIL-R3, TRAILR3, TRID | 603613 |
ID: 489 | ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (3923873..3964437, complement) | SERCA3 | 601929 |
ID: 391 | ras homolog family member G [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (3826978..3840959, complement) | ARHG | 179505 |
ID: 5878 | RAB5C, member RAS oncogene family [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42124979..42154989, complement) | L1880L, RAB5L, RABL, RAB5C | 604037 |
ID: 9056 | solute carrier family 7 member 7 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (22773222..22819791, complement) | LAT3, LPI, MOP-2, Y+LAT1, y+LAT-1 | 603593 |
ID: 5881 | Rac family small GTPase 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82031678..82034204) | | 602050 |
ID: 29984 | ras homolog family member D [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (67056847..67072017) | ARHD, RHOHP1, RHOM, Rho | 605781 |
ID: 29121 | C-type lectin domain family 2 member D [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (9669713..9699553) | CLAX, LLT1, OCIL | 605659 |