ID: 92737 | delta/notch like EGF repeat containing [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (229357629..229714555, complement) | UNQ26, bet | 607299 |
ID: 9699 | regulating synaptic membrane exocytosis 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (103500610..104256094) | CRSDS, OBOE, RAB3IP3, RIM2 | 606630 |
ID: 51761 | ATPase phospholipid transporting 8A2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (25371974..26025851) | ATP, ATPIB, CAMRQ4, IB, ML-1 | 605870 |
ID: 284338 | proline rich 19 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (42302132..42310814) | | |
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: 27285 | tektin 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (36084094..36088275) | TEKTB1, TEKTIN-T, h-tektin-t | 608953 |
ID: 84465 | multiple EGF like domains 11 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (65895299..66253750, complement) | | 612454 |
ID: 222950 | neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100483927..100494802) | C7orf51 | 615477 |
ID: 8193 | double PHD fingers 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38211006..38229695, complement) | BAF45b, NEUD4, SMARCG1, neuro-d4 | 601670 |
ID: 4917 | netrin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2471297..2474145) | NTN2L | 602349 |
ID: 146664 | alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (76868404..76950393) | GnT-IX, GnT-VB | 612441 |
ID: 57540 | dispatched RND transporter family member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11479155..11537551) | PTCHD2 | 611251 |
ID: 8448 | double C2 domain alpha [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30005514..30023228, complement) | Doc2 | 604567 |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 4185 | ADAM metallopeptidase domain 11 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44758988..44781846) | MDC | 155120 |
ID: 58157 | neuroglobin [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77265483..77271206, complement) | | 605304 |
ID: 200150 | phospholipase D family member 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (242082986..242530546, complement) | PLDC | |
ID: 91663 | myeloid associated differentiation marker [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (53865628..53876435) | SB135 | 609959 |
ID: 56896 | dihydropyrimidinase like 5 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (26847995..26950351) | CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6 | 608383 |
ID: 2676 | GDNF family receptor alpha 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (138252380..138274621, complement) | GDNFR3 | 605710 |