| ID: 6505 | solute carrier family 1 member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (4490468..4587469) | DCBXA, EAAC1, EAAT3, SCZD18, hEAAC1 | 133550 |
| ID: 351 | amyloid beta precursor protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (25880550..26171128, complement) | AAA, ABETA, ABPP, AD1I, CTFgamma, CVAP, PN-II, PN2, alpha-sAPP, preA4, APP | 104760 |
| 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: 7852 | C-X-C motif chemokine receptor 4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (136114349..136118149, complement) | CD184, D2S201E, FB22, HM89, HSY3RR, LAP-3, LAP3, LCR1, LESTR, NPY3R, NPYR, NPYRL, NPYY3R, WHIM, WHIMS, WHIMS1 | 162643 |
| ID: 3119 | major histocompatibility complex, class II, DQ beta 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32659467..32666657, complement) | CELIAC1, HLA-DQB, IDDM1 | 604305 |
| 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: 5663 | presenilin 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (73136417..73223691) | ACNINV3, AD3, CMD1U, FAD, PS-1, PS1, PSNL1, S182 | 104311 |
| ID: 5578 | protein kinase C alpha [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (66302613..66810743) | AAG6, PKC-alpha, PKCA, PKCI+/-, PKCalpha, PRKACA | 176960 |
| ID: 2260 | fibroblast growth factor receptor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38411143..38468635, complement) | BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 | 136350 |
| ID: 558 | AXL receptor tyrosine kinase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (41219223..41261766) | ARK3, JTK11, Tyro7, UFO, AXL | 109135 |
| ID: 2130 | EWS RNA binding protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29268268..29300521) | EWS, EWS-FLI1, bK984G1.4 | 133450 |
| ID: 2904 | glutamate ionotropic receptor NMDA type subunit 2B [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (13537337..13982134, complement) | DEE27, EIEE27, GluN2B, MRD6, NMDAR2B, NR2B, NR3, hNR3 | 138252 |
| ID: 3716 | Janus kinase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (64833229..65067746, complement) | AIIDEA, JAK1B, JTK3, JAK1 | 147795 |
| ID: 8795 | TNF receptor superfamily member 10b [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23020133..23069031, complement) | CD262, DR5, KILLER, KILLER/DR5, TRAIL-R2, TRAILR2, TRICK2, TRICK2A, TRICK2B, TRICKB, ZTNFR9 | 603612 |
| ID: 3965 | galectin 9 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (27631188..27649560) | HUATA, LGALS9 | 601879 |
| ID: 2902 | glutamate ionotropic receptor NMDA type subunit 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (137139154..137168756) | DEE101, GluN1, MRD8, NDHMSD, NDHMSR, NMD-R1, NMDA1, NMDAR1, NR1 | 138249 |
| ID: 360 | aquaporin 3 (Gill blood group) [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (33441160..33447593, complement) | AQP-3, GIL | 600170 |
| ID: 2903 | glutamate ionotropic receptor NMDA type subunit 2A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (9753404..10182908, complement) | EPND, FESD, GluN2A, LKS, NMDAR2A, NR2A | 138253 |
| ID: 58191 | C-X-C motif chemokine ligand 16 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4733533..4739928, complement) | CXCLG16, SR-PSOX, SRPSOX | 605398 |
| ID: 407015 | microRNA 26a-1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (37969404..37969480) | MIR26A, MIRN26A1, mir-26a-1 | 612151 |