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: 196500 | PILR alpha associated neural protein [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6692178..6700815, complement) | C12orf53, LEDA1, PANP, leda-1 | 616065 |
ID: 4917 | netrin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2471297..2474145) | NTN2L | 602349 |
ID: 1808 | dihydropyrimidinase like 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (26514031..26658175) | CRMP-2, CRMP2, DHPRP2, DRP-2, DRP2, N2A3, ULIP-2, ULIP2 | 602463 |
ID: 286183 | sodium/potassium transporting ATPase interacting 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (62248854..62999652) | FAM77D-IT1, UG0898H09, NKAIN3 | 612872 |
ID: 10570 | dihydropyrimidinase like 4 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (132186948..132205759) | CRMP3, DRP-4, ULIP4 | 608407 |
ID: 84446 | BR serine/threonine kinase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (55283997..55312562) | SAD-B, hSAD1 | 609235 |
ID: 10687 | PNMA family member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (26504701..26513872, complement) | MA2, MM2, RGAG2 | 603970 |
ID: 219409 | GS homeobox 1 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27792483..27794768) | GSH1, Gsh-1 | 616542 |
ID: 201191 | sterile alpha motif domain containing 14 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (50110040..50130160, complement) | | 619233 |
ID: 6664 | SRY-box transcription factor 11 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (5692384..5701385) | CSS9, IDDMOH, MRD27 | 600898 |
ID: 64748 | phospholipid phosphatase related 2 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (11355432..11365698) | LPPR2, PRG4 | 619591 |
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: 717 | complement C2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31897783..31945672) | ARMD14, CO2 | 613927 |
ID: 57699 | copine 5 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (36740775..36839998, complement) | COPN5, CPN5 | 604209 |
ID: 57169 | zinc finger NFX1-type containing 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49245900..49278057, complement) | IMD91 | 618931 |
ID: 222950 | neuronal tyrosine phosphorylated phosphoinositide-3-kinase adaptor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100483927..100494802) | C7orf51 | 615477 |
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: 197407 | zinc finger protein 48 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30378312..30400108) | ZNF553 | |
ID: 259236 | transmembrane inner ear [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (46693778..46710886) | DFNB6 | 607237 |