ID: 79993 | ELOVL fatty acid elongase 7 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (60751791..60844269, complement) | | 614451 |
ID: 151230 | kelch like family member 23 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (169733832..169751878) | DITHP | |
ID: 57630 | SH3 domain containing ring finger 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (169094259..169270956, complement) | POSH, RNF142, SH3MD2 | 618642 |
ID: 55225 | ribonucleoprotein, PTB binding 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (64745075..64833232) | | 609953 |
ID: 3382 | islet cell autoantigen 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (8113184..8262555, complement) | ICA69, ICAp69 | 147625 |
ID: 27347 | serine/threonine kinase 39 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (167954022..168247595, complement) | DCHT, PASK, SPAK | 607648 |
ID: 123096 | solute carrier family 25 member 29 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (100278567..100306444, complement) | C14orf69, CACL, ORNT3 | 615064 |
ID: 6714 | SRC proto-oncogene, non-receptor tyrosine kinase [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (37344699..37406050) | ASV1, THC6, c-SRC, p60-Src, SRC | 190090 |
ID: 81563 | chromosome 1 open reading frame 21 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (184387029..184629019) | PIG13 | |
ID: 5763 | parathymosin [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (6766363..6770952) | ParaT | 168440 |
ID: 54492 | neuralized E3 ubiquitin protein ligase 1B [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (172641263..172691540) | NEURL3, RNF67B, hNeur2, neur2 | 615893 |
ID: 26064 | retinoic acid induced 14 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (34656328..34832612) | NORPEG, RAI13 | 606586 |
ID: 84612 | par-6 family cell polarity regulator beta [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50731580..50753741) | PAR6B | 608975 |
ID: 783 | calcium voltage-gated channel auxiliary subunit beta 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (18140424..18543557) | CAB2, CACNLB2, CAVB2, MYSB | 600003 |
ID: 6304 | SATB homeobox 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (18345377..18445592, complement) | DEFDA, DHDBV, KTZSL | 602075 |
ID: 9189 | zinc finger BED-type containing 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (2486435..2500976, complement); Chromosome Y, NC_000024.10 (2486435..2500976, complement) | ALTE, DREF, TRAMP, hDREF | 300178 |
ID: 10771 | zinc finger MYND-type containing 11 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (130088..254637) | BRAM1, BS69, MRD30 | 608668 |
ID: 6483 | ST3 beta-galactoside alpha-2,3-sialyltransferase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (70375977..70439100, complement) | Gal-NAc6S, SIAT4B, ST3GALII, ST3GalA.2 | 607188 |
ID: 27445 | piccolo presynaptic cytomatrix protein [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (82754012..83162884, complement) | ACZ, PCH3 | 604918 |
ID: 6888 | transaldolase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (747464..765012) | TAL, TAL-H, TALDOR, TALH | 602063 |