ID: 57460 | protein phosphatase, Mg2+/Mn2+ dependent 1H [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (62643994..62935150, complement) | ARHCL1, NERPP-2C, URCC2 | 616016 |
ID: 51527 | GSK3B interacting protein [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96363526..96387290) | C14orf129, HSPC210 | 616605 |
ID: 84858 | zinc finger protein 503 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (75279725..75401916, complement) | NOLZ-1, NOLZ1, Nlz2 | 613902 |
ID: 192111 | PGAM family member 5, mitochondrial serine/threonine protein phosphatase [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (132710842..132722734) | BXLBV68 | 614939 |
ID: 93058 | coenzyme Q10A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56266942..56270966) | | 620736 |
ID: 55102 | autophagy related 2B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96279195..96363341, complement) | BLTP4B, C14orf103 | 616226 |
ID: 55829 | selenoprotein S [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (101270809..101277485, complement) | AD-015, ADO15, SBBI8, SELS, SEPS1, VIMP | 607918 |
ID: 195827 | peroxiredoxin like 2C [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96639577..96655317, complement) | AAED1, C9orf21 | |
ID: 2874 | G protein pathway suppressor 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7312661..7315360, complement) | AMF-1 | 601935 |
ID: 4734 | NEDD4 E3 ubiquitin protein ligase [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (55826917..55993612, complement) | NEDD4-1, RPF1 | 602278 |
ID: 55680 | RUN and FYVE domain containing 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (68341112..68407277, complement) | RABIP4R, ZFYVE13 | 610328 |
ID: 54536 | exocyst complex component 6 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92826831..93059490) | EXOC6A, SEC15, SEC15L, SEC15L1, SEC15L3, Sec15p | 609672 |
ID: 55342 | spermatid perinuclear RNA binding protein [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (123109494..123268586, complement) | HEL162, ILF3L, SPNR, p74 | 611138 |
ID: 57542 | kelch like family member 42 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (27780233..27803040) | Ctb9, KLHDC5 | 618919 |
ID: 10257 | ATP binding cassette subfamily C member 4 (PEL blood group) [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95019835..95301451, complement) | MOAT-B, MOATB, MRP4 | 605250 |
ID: 55103 | Ral GEF with PH domain and SH3 binding motif 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (178725244..178921840) | dJ595C2.1 | 617819 |
ID: 84629 | trinucleotide repeat containing 18 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (5306811..5423834, complement) | CAGL79A, TNRC18 | 620902 |
ID: 283373 | ankyrin repeat domain 52 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (56237807..56258384, complement) | ANKRD33, ARSC | 620862 |
ID: 127829 | ARF like GTPase 8A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (202133404..202144737, complement) | ARL10B, GIE2 | 616597 |
ID: 1820 | AT-rich interaction domain 3A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (925732..975939) | BRIGHT, DRIL1, DRIL3, E2FBP1 | 603265 |