ID: 90007 | midnolin [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (1248583..1259143) | Stx | 606700 |
ID: 51022 | glutaredoxin 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (193096465..193106114, complement) | CGI-133, GRX2 | 606820 |
ID: 6717 | sorcin [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (88205115..88226976, complement) | CP-22, CP22, SCN, V19 | 182520 |
ID: 51006 | solute carrier family 35 member C2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46345984..46364425, complement) | BA394O2.1, C20orf5, CGI-15, OVCOV1 | 619530 |
ID: 23303 | kinesin family member 13B [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (29067278..29263388, complement) | GAKIN | 607350 |
ID: 79058 | ASPSCR1 tether for SLC2A4, UBX domain containing [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81977629..82017406) | ASPCR1, ASPL, ASPS, RCC17, TUG, UBXD9, UBXN9 | 606236 |
ID: 85015 | ubiquitin specific peptidase 45 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (99432325..99517846, complement) | LCA19 | 618439 |
ID: 339448 | chromosome 1 open reading frame 174 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (3889133..3900272, complement) | | |
ID: 7326 | ubiquitin conjugating enzyme E2 G1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (4269259..4366675, complement) | E217K, UBC7, UBE2G | 601569 |
ID: 23461 | ATP binding cassette subfamily A member 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (69244311..69327133, complement) | ABC13, DEL17q24, EST90625, HTC3, HTGH | 612503 |
ID: 51094 | adiponectin receptor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202940825..202958572, complement) | ACDCR1, CGI-45, CGI45, PAQR1, TESBP1A | 607945 |
ID: 23493 | hes related family bHLH transcription factor with YRPW motif 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (125749632..125761269) | CHF1, GRIDLOCK, GRL, HERP1, HESR2, HRT2, bHLHb32 | 604674 |
ID: 57719 | anoctamin 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17323223..17334855, complement) | KIAA1623, TMEM16H | 610216 |
ID: 26608 | transducin beta like 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (73567537..73578579, complement) | WBSCR13, WS-betaTRP | 605842 |
ID: 51668 | intraflagellar transport 25 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (53911576..53946305, complement) | C1orf41, CFAP232, FAP232, HSPB11, HSPCO34, PP25 | 620841 |
ID: 199990 | FA core complex associated protein 20 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (2184477..2212720, complement) | C1orf86, FP7162 | 615183 |
ID: 55343 | solute carrier family 35 member C1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (45804079..45813016) | CDG2C, FUCT1 | 605881 |
ID: 200014 | coiled-coil and C2 domain containing 1B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (52350597..52366205, complement) | Lgd1 | |
ID: 8624 | proteasome assembly chaperone 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39174769..39183514, complement) | C21LRP, DSCR2, LRPC21, PAC-1, PAC1, Pba1 | 605296 |
ID: 388886 | leucine rich repeat containing 75B [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24585635..24593073, complement) | C22orf36, FAM211B | |