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: 10683 | delta like canonical Notch ligand 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (39498947..39508469) | SCDO1 | 602768 |
ID: 27164 | spalt like transcription factor 3 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78979818..78998969) | ZNF796 | 605079 |
ID: 3208 | hippocalcin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32885996..32894646) | BDR2, DYT2 | 142622 |
ID: 2912 | glutamate metabotropic receptor 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (51707068..51718613) | GLUR2, GPRC1B, MGLUR2, mGlu2 | 604099 |
ID: 643669 | coiled-coil glutamate rich protein 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38908980..38912186, complement) | | 617634 |
ID: 440073 | IQ motif and Sec7 domain ArfGEF 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (66767..178455) | | 612118 |
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: 51286 | cell cycle exit and neuronal differentiation 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (787115..790090, complement) | BM88 | 608213 |
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: 79948 | phospholipid phosphatase related 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (812488..823797, complement) | LPPR3, LPR3, PRG-2, PRG2 | 610391 |
ID: 54734 | RAB39A, member RAS oncogene family [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107928448..107963482) | K28, RAB39 | 619558 |
ID: 27133 | potassium voltage-gated channel subfamily H member 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (62699464..63045458, complement) | DEE112, EAG2, H-EAG2, Kv10.2, hEAG2 | 605716 |
ID: 55871 | Zn regulated GTPase metalloprotein activator 1A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120837..179056, complement) | CBWD1, COBP | 611078 |
ID: 56341 | protein arginine methyltransferase 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (3381349..3593973) | HRMT1L3, HRMT1L4 | 610086 |
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: 11166 | SRY-box transcription factor 21 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94709622..94712545, complement) | SOX25 | 604974 |
ID: 5458 | POU class 4 homeobox 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (146638893..146642474) | BRN3.2, BRN3B, Brn-3b | 113725 |
ID: 94030 | leucine rich repeat containing 4B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50516892..50568435, complement) | HSM, LRIG4, NGL-3 | |
ID: 4744 | neurofilament heavy chain [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29480218..29491390) | CMT2CC, NFH | 162230 |