ID: 124565 | solute carrier family 38 member 10 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81244811..81295307, complement) | PP1744, SNAT10 | 616525 |
ID: 7157 | tumor protein p53 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7668421..7687490, complement) | BCC7, BMFS5, LFS1, P53, TRP53 | 191170 |
ID: 3077 | homeostatic iron regulator [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (26087429..26098343) | HFE1, HH, HLA-H, MVCD7, TFQTL2 | 613609 |
ID: 4089 | SMAD family member 4 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (51030213..51085042) | DPC4, JIP, MADH4, MYHRS | 600993 |
ID: 3117 | major histocompatibility complex, class II, DQ alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32637406..32655272) | CELIAC1, DQ-A1, DQA1, HLA-DQA*, HLA-DQB1, HLA-DQA1 | 146880 |
ID: 3084 | neuregulin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (31639245..32774046) | ARIA, GGF, GGF2, HGL, HRG, HRG1, HRGA, MST131, MSTP131, NDF-IT2, SMDF, NRG1 | 142445 |
ID: 9817 | kelch like ECH associated protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10486125..10503356, complement) | INrf2, KLHL19 | 606016 |
ID: 5045 | furin, paired basic amino acid cleaving enzyme [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90868588..90883457) | FUR, PACE, PCSK3, SPC1 | 136950 |
ID: 1901 | sphingosine-1-phosphate receptor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (101236899..101242313) | CD363, CHEDG1, D1S3362, ECGF1, EDG-1, EDG1, S1P1 | 601974 |
ID: 1859 | dual specificity tyrosine phosphorylation regulated kinase 1A [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37365573..37526358) | DYRK, DYRK1, HP86, MNB, MNBH, MRD7 | 600855 |
ID: 2548 | alpha glucosidase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80101581..80119881) | LYAG | 606800 |
ID: 6329 | sodium voltage-gated channel alpha subunit 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (63938554..63972918, complement) | CMS16, CMYO22A, CMYP22A, HOKPP2, HYKPP, HYPP, NAC1A, Na(V)1.4, Nav1.4, SkM1 | 603967 |
ID: 3122 | major histocompatibility complex, class II, DR alpha [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32439887..32445046) | HLA-DRA1 | 142860 |
ID: 1137 | cholinergic receptor nicotinic alpha 4 subunit [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63343223..63361349, complement) | BFNC, EBN, EBN1, NACHR, NACHRA4, NACRA4 | 118504 |
ID: 8405 | speckle type BTB/POZ protein [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49598884..49678163, complement) | BTBD32, NEDMACE, NEDMIDF, NSDVS1, NSDVS2, TEF2 | 602650 |
ID: 10456 | HCLS1 associated protein X-1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (154272629..154275875) | HCLSBP1, HS1BP1, SCN3 | 605998 |
ID: 3113 | major histocompatibility complex, class II, DP alpha 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33064569..33080748, complement) | DP(W3), DP(W4), DPA1, HLA-DP1A, HLA-DPA, HLA-DPB1, HLADP, HLASB, PLT1 | 142880 |
ID: 3799 | kinesin family member 5B [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (32009015..32056425, complement) | HEL-S-61, KINH, KNS, KNS1, UKHC | 602809 |
ID: 57721 | methyltransferase 14, N6-adenosine-methyltransferase non-catalytic subunit [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (118685392..118715430) | hMETTL14 | 616504 |
ID: 5479 | peptidylprolyl isomerase B [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (64155817..64163022, complement) | CYP-S1, CYPB, HEL-S-39, OI9, SCYLP | 123841 |