| ID: 8448 | double C2 domain alpha [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30005514..30023228, complement) | Doc2 | 604567 |
| ID: 7476 | Wnt family member 7A [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (13816258..13880071, complement) | Wnt-7a | 601570 |
| ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
| ID: 6572 | solute carrier family 18 member A3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49610310..49612720) | CMS21, VACHT | 600336 |
| ID: 8193 | double PHD fingers 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38211006..38229695, complement) | BAF45b, NEUD4, SMARCG1, neuro-d4 | 601670 |
| ID: 9118 | internexin neuronal intermediate filament protein alpha [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (103277138..103290346) | NEF5, NF-66, NF66, TXBP-1 | 605338 |
| ID: 9143 | synaptogyrin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1989970..1994275) | | 603927 |
| ID: 171177 | ras homolog family member V [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40872214..40874234, complement) | ARHV, CHP, WRCH2 | 620101 |
| ID: 126567 | C2 calcium dependent domain containing 4C [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (405445..409147, complement) | FAM148C, KIAA1957, NLF3 | 610336 |
| ID: 161357 | MAM domain containing glycosylphosphatidylinositol anchor 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (46839623..47675605, complement) | MAMDC1, c14_5286 | 611128 |
| ID: 51761 | ATPase phospholipid transporting 8A2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (25371974..26025851) | ATP, ATPIB, CAMRQ4, IB, ML-1 | 605870 |
| ID: 58157 | neuroglobin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77265483..77271206, complement) | | 605304 |
| ID: 4054 | latent transforming growth factor beta binding protein 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65538559..65558359, complement) | DASS, GPHYSD3, LTBP-3, LTBP2, STHAG6, pp6425 | 602090 |
| ID: 92737 | delta/notch like EGF repeat containing [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (229357629..229714555, complement) | UNQ26, bet | 607299 |
| ID: 51477 | inositol-3-phosphate synthase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18434388..18438133, complement) | INO1, INOS, IPS, IPS 1, IPS-1 | 611670 |
| ID: 4185 | ADAM metallopeptidase domain 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44758988..44781846) | MDC | 155120 |
| ID: 9715 | family with sequence similarity 131 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143353400..143382304, complement) | | 619282 |
| ID: 9478 | calcium binding protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120640626..120680866) | CALBRAIN, HCALB_BR | 605563 |
| ID: 482 | ATPase Na+/K+ transporting subunit beta 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7646627..7657770) | AMOG | 182331 |
| ID: 4917 | netrin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2471297..2474145) | NTN2L | 602349 |