ID: 4917 | netrin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2471297..2474145) | NTN2L | 602349 |
ID: 201191 | sterile alpha motif domain containing 14 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50110040..50130160, complement) | | 619233 |
ID: 196500 | PILR alpha associated neural protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6692178..6700815, complement) | C12orf53, LEDA1, PANP, leda-1 | 616065 |
ID: 9196 | potassium voltage-gated channel subfamily A regulatory beta subunit 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7921859..7929856, complement) | AKR6A9, KCNA3.1B, KCNA3B, KV-BETA-3 | 604111 |
ID: 2583 | beta-1,4-N-acetyl-galactosaminyltransferase 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57623409..57633201, complement) | GALGT, GALNACT, GalNAc-T, SPG26 | 601873 |
ID: 222950 | neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100483927..100494802) | C7orf51 | 615477 |
ID: 84446 | BR serine/threonine kinase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55283997..55312562) | SAD-B, hSAD1 | 609235 |
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: 6572 | solute carrier family 18 member A3 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (49610310..49612720) | CMS21, VACHT | 600336 |
ID: 9699 | regulating synaptic membrane exocytosis 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (103500610..104256094) | CRSDS, OBOE, RAB3IP3, RIM2 | 606630 |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 8193 | double PHD fingers 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38211006..38229695, complement) | BAF45b, NEUD4, SMARCG1, neuro-d4 | 601670 |
ID: 51761 | ATPase phospholipid transporting 8A2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (25371974..26025851) | ATP, ATPIB, CAMRQ4, IB, ML-1 | 605870 |
ID: 92737 | delta/notch like EGF repeat containing [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (229357629..229714555, complement) | UNQ26, bet | 607299 |
ID: 56917 | Meis homeobox 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47403124..47422233, complement) | MRG2 | 619443 |
ID: 85442 | kinase non-catalytic C-lobe domain containing 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (133160219..133226412) | C10orf23, RASGEF2, Very-KIND, bB439H18.3, v-KIND | 616237 |
ID: 57449 | pleckstrin homology and RhoGEF domain containing G5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6467122..6520092, complement) | ARHGEF45, CMTRIC, DSMA4, GEF720, HMNR4, Syx, Tech | 611101 |
ID: 284338 | proline rich 19 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (42302132..42310814) | | |
ID: 9715 | family with sequence similarity 131 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (143353400..143382304, complement) | | 619282 |
ID: 54849 | differentially expressed in FDCP 8 homolog [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89948755..89968060) | | |