ID: 22983 | microtubule associated serine/threonine kinase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12838515..12874952) | MCCCHCM, SAST | 612256 |
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: 3208 | hippocalcin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32885996..32894646) | BDR2, DYT2 | 142622 |
ID: 343702 | XK related 7 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (31968151..32003387) | C20orf159, dJ310O13.4 | |
ID: 146330 | F-box and leucine rich repeat protein 16 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (692500..705801, complement) | C16orf22, Fbl16, c380A1.1 | 609082 |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 286 | ankyrin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (41653225..41896741, complement) | ANK, SPH1, SPH2, ankyrin-1 | 612641 |
ID: 79948 | phospholipid phosphatase related 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (812488..823797, complement) | LPPR3, LPR3, PRG-2, PRG2 | 610391 |
ID: 11166 | SRY-box transcription factor 21 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94709622..94712545, complement) | SOX25 | 604974 |
ID: 60482 | solute carrier family 5 member 7 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (107986524..108013994) | CHT, CHT1, CMS20, DHMNVP, HMN7A, HMND7, hCHT1 | 608761 |
ID: 56341 | protein arginine methyltransferase 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (3381349..3593973) | HRMT1L3, HRMT1L4 | 610086 |
ID: 2290 | forkhead box G1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (28766787..28770277) | BF1, BF2, FHKL3, FKH2, FKHL1, FKHL2, FKHL3, FKHL4A, FOXG1B, FOXG1C, HBF-1, HBF-2, HBF-3, HBF-G2, HBF2, HFK1, HFK2, HFK3, KHL2, QIN, FOXG1 | 164874 |
ID: 220107 | deleted in lymphocytic leukemia 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50711026..50843939, complement) | | 618634 |
ID: 440073 | IQ motif and Sec7 domain ArfGEF 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (66767..178455) | | 612118 |
ID: 222183 | serine/arginine repetitive matrix 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76201896..76287287) | | |
ID: 60677 | CUGBP Elav-like family member 6 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72284727..72320157, complement) | BRUNOL6 | 612681 |
ID: 4744 | neurofilament heavy chain [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29480218..29491390) | CMT2CC, NFH | 162230 |
ID: 283576 | zinc finger DHHC-type palmitoyltransferase 22 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77131270..77142288, complement) | C14orf59 | |
ID: 53822 | FXYD domain containing ion transport regulator 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35143255..35154302) | | 606684 |
ID: 643669 | coiled-coil glutamate rich protein 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38908980..38912186, complement) | | 617634 |