ID: 11166 | SRY-box transcription factor 21 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94709622..94712545, complement) | SOX25 | 604974 |
ID: 643669 | coiled-coil glutamate rich protein 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38908980..38912186, complement) | | 617634 |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 4744 | neurofilament heavy chain [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29480218..29491390) | CMT2CC, NFH | 162230 |
ID: 27164 | spalt like transcription factor 3 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78979818..78998969) | ZNF796 | 605079 |
ID: 222183 | serine/arginine repetitive matrix 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76201896..76287287) | | |
ID: 2736 | GLI family zinc finger 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (120735868..120992653) | CJS, HPE9, PHS2, THP1, THP2 | 165230 |
ID: 220107 | deleted in lymphocytic leukemia 7 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (50711026..50843939, complement) | | 618634 |
ID: 374887 | YjeF N-terminal domain containing 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (19528911..19537581) | | 618607 |
ID: 94030 | leucine rich repeat containing 4B [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50516892..50568435, complement) | HSM, LRIG4, NGL-3 | |
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: 4761 | neuronal differentiation 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39603768..39607920, complement) | DEE72, EIEE72, NDRF, bHLHa1 | 601725 |
ID: 1113 | chromogranin A [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (92922664..92935285) | CGA, PHE5, PHES | 118910 |
ID: 375607 | N-acetyltransferase 16 (putative) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101170496..101180293, complement) | C7orf52 | 615783 |
ID: 132204 | synaptoporin [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (63200604..63616924) | SPO | |
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: 7425 | VGF nerve growth factor inducible [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101162509..101169952, complement) | SCG7, SgVII | 602186 |
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: 56341 | protein arginine methyltransferase 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (3381349..3593973) | HRMT1L3, HRMT1L4 | 610086 |
ID: 53822 | FXYD domain containing ion transport regulator 7 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35143255..35154302) | | 606684 |