ID: 10900 | RUN domain containing 3A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44308601..44318670) | RAP2IP, RPIP-8, RPIP8 | 605448 |
ID: 2912 | glutamate metabotropic receptor 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (51707068..51718613) | GLUR2, GPRC1B, MGLUR2, mGlu2 | 604099 |
ID: 116986 | ArfGAP with GTPase domain, ankyrin repeat and PH domain 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (57723761..57742161, complement) | CENTG1, GGAP2, PIKE | 605476 |
ID: 5458 | POU class 4 homeobox 2 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (146638893..146642474) | BRN3.2, BRN3B, Brn-3b | 113725 |
ID: 3904 | leukocyte associated immunoglobulin like receptor 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (54502831..54510687) | CD306 | 602993 |
ID: 729993 | shisa family member 9 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (12901598..13563017) | CKAMP44 | 613346 |
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: 22865 | SLIT and NTRK like family member 3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (165186720..165197109, complement) | | 609679 |
ID: 51286 | cell cycle exit and neuronal differentiation 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (787115..790090, complement) | BM88 | 608213 |
ID: 375612 | LHFPL tetraspan subfamily member 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (104328603..104908561) | LHFPL4 | 609719 |
ID: 132204 | synaptoporin [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (63200604..63616924) | SPO | |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 10683 | delta like canonical Notch ligand 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (39498947..39508469) | SCDO1 | 602768 |
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: 126567 | C2 calcium dependent domain containing 4C [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (405445..409147, complement) | FAM148C, KIAA1957, NLF3 | 610336 |
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: 57699 | copine 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (36740775..36839998, complement) | COPN5, CPN5 | 604209 |
ID: 8193 | double PHD fingers 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (38211006..38229695, complement) | BAF45b, NEUD4, SMARCG1, neuro-d4 | 601670 |
ID: 5144 | phosphodiesterase 4D [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (58969038..60522128, complement) | ACRDYS2, DPDE3, HSPDE4D, PDE43N2, STRK1, PDE4D | 600129 |
ID: 285175 | unc-80 homolog, NALCN channel complex subunit [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (209771832..209999296) | C2orf21, UNC-80 | 612636 |