ID: 4609 | MYC proto-oncogene, bHLH transcription factor [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (127735434..127742951) | MRTLC, bHLHe39, c-Myc, MYC | 190080 |
ID: 4247 | alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (49620799..49623481) | CDG2A, CDGS2, GLCNACTII, GNT-II, GNT2 | 602616 |
ID: 9252 | ribosomal protein S6 kinase A5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (90847861..91060641, complement) | MSK1, MSPK1, RLPK | 603607 |
ID: 65244 | spermatogenesis associated serine rich 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49366852..49527425) | Nbla00526, P59SCR, SCR59, SPATA10 | 611667 |
ID: 4221 | menin 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (64803516..64811294, complement) | MEAI, SCG2 | 613733 |
ID: 254863 | transmembrane protein 256 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7402975..7404097, complement) | C17orf61 | 617779 |
ID: 10921 | RNA binding protein with serine rich domain 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2253116..2268126, complement) | E5.1 | 606447 |
ID: 23384 | sperm antigen with calponin homology and coiled-coil domains 1 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (24270831..24417738) | CYTSA, GBBB2, OBLFC1, TBHS, TBHS1 | 614140 |
ID: 4659 | protein phosphatase 1 regulatory subunit 12A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (79773563..79935460, complement) | GUBS, M130, MBS, MYPT1 | 602021 |
ID: 7419 | voltage dependent anion channel 3 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (42391880..42405937) | HD-VDAC3, VDAC-3 | 610029 |
ID: 80196 | ring finger protein 34 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (121400118..121424348) | CARP-1, CARP1, RFI, RIF, RIFF, hRFI | 608299 |
ID: 29959 | nuclear receptor binding protein 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27427790..27442259) | BCON3, MADM, MUDPNP, NRBP | 606010 |
ID: 6867 | transforming acidic coiled-coil containing protein 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38728582..38853028) | Ga55 | 605301 |
ID: 22858 | ciliogenesis associated kinase 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53001303..53061824, complement) | ECO, EJM10, ICK, LCK2, MRK, hICK | 612325 |
ID: 124565 | solute carrier family 38 member 10 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (81244811..81295307, complement) | PP1744, SNAT10 | 616525 |
ID: 51160 | VPS28 subunit of ESCRT-I [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144423617..144428548, complement) | CIIA | 611952 |
ID: 4300 | MLLT3 super elongation complex subunit [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (20341669..20622499, complement) | AF9, YEATS3 | 159558 |
ID: 10400 | phosphatidylethanolamine N-methyltransferase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17505563..17592142, complement) | PEAMT, PEMPT2, PLMT, PNMT, PEMT | 602391 |
ID: 9926 | lysophosphatidylglycerol acyltransferase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (211743457..211830763, complement) | FAM34A, FAM34A1, LPLAT7, NET8 | 610473 |
ID: 8509 | N-deacetylase and N-sulfotransferase 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (73801916..73811820, complement) | HSST2, N-HSST 2, NST2 | 603268 |