ID: 51330 | TNF receptor superfamily member 12A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (3020368..3022383) | CD266, FN14, TWEAKR | 605914 |
ID: 4318 | matrix metallopeptidase 9 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46008908..46016561) | CLG4B, GELB, MANDP2, MMP-9 | 120361 |
ID: 999 | cadherin 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68737292..68835537) | Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM, UVO | 192090 |
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: 328 | apurinic/apyrimidinic endodeoxyribonuclease 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (20455226..20457767) | APE, APE1, APEN, APEX, APX, HAP1, REF1 | 107748 |
ID: 7186 | TNF receptor associated factor 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136881958..136926607) | MGC:45012, RNF117, TRAP, TRAP3 | 601895 |
ID: 7187 | TNF receptor associated factor 3 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (102777449..102911500) | CAP-1, CAP1, CD40bp, CRAF1, IIAE5, LAP1, RNF118 | 601896 |
ID: 8742 | TNF superfamily member 12 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7549058..7557881) | APO3L, DR3LG, TNLG4A, TWEAK | 602695 |
ID: 329 | baculoviral IAP repeat containing 2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (102347214..102378670) | API1, HIAP2, Hiap-2, MIHB, RNF48, c-IAP1, cIAP1 | 601712 |
ID: 7185 | TNF receptor associated factor 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120902393..120929171, complement) | EBI6, MGC:10353 | 601711 |
ID: 7850 | interleukin 1 receptor type 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (101991960..102028544) | CD121b, CDw121b, IL-1R-2, IL-1RT-2, IL-1RT2c, IL1RB, IL1R2 | 147811 |
ID: 3187 | heterogeneous nuclear ribonucleoprotein H1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179614178..179634784, complement) | HNRPH, HNRPH1, NEDCDS, hnRNPH | 601035 |
ID: 7188 | TNF receptor associated factor 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (211326635..211374946) | MGC:39780, RNF84 | 602356 |
ID: 25797 | glutaminyl-peptide cyclotransferase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (37344630..37373322) | GCT, QC, sQC | 607065 |
ID: 51043 | zinc finger and BTB domain containing 7B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (155001750..155018523) | CKROX, THPOK, ZBTB15, ZFP-67, ZFP67, ZNF857B, c-KROX, hcKROX, vGAF | 607646 |
ID: 7780 | solute carrier family 30 member 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (26037252..26046118, complement) | PP12488, TNZD, ZNT2, ZnT-2 | 609617 |
ID: 8796 | sciellin [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (77535706..77645263) | | 604112 |
ID: 85293 | keratin associated protein 3-3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (40993430..40994164, complement) | KAP3.3, KRTAP3.3 | |