ID: 65990 | adenine nucleotide translocase lysine methyltransferase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (721146..722590) | ANT-KMT, C16orf24, FAM173A | 618566 |
ID: 55795 | PCI domain containing 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113165002..113208669, complement) | F10 | 613713 |
ID: 123872 | dynein axonemal assembly factor 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (84145308..84177920) | CILD13, DAU1, LRRC50, ODA7, swt | 613190 |
ID: 8451 | cullin 4A [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (113208193..113267108) | | 603137 |
ID: 285755 | peptidylprolyl isomerase like 6 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (109390215..109441171, complement) | PPIase, RSPH12, bA425D10.6, dJ919F19.1 | |
ID: 64223 | MTOR associated protein, LST8 homolog [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (2205454..2209453) | GBL, GbetaL, LST8, POP3, WAT1 | 612190 |
ID: 64426 | SDS3 homolog, SIN3A corepressor complex component [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (118376555..118418033) | SAP45, SDS3 | 608250 |
ID: 90120 | transmembrane protein 250 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136114589..136118875, complement) | C9orf69 | |
ID: 81533 | integrin alpha FG-GAP repeat containing 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (47154391..47461246, complement) | 2310047C21Rik, CDA08, LINKIN, LNKN-1, TIP | 611803 |
ID: 93081 | testis expressed 30 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (102765888..102773786, complement) | C13orf27 | |
ID: 8824 | carboxylesterase 2 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (66934471..66945096) | CE-2A1, PCE-2, iCE, CES2 | 605278 |
ID: 26233 | F-box and leucine rich repeat protein 6 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144355431..144358472, complement) | FBL6, FBL6A, PP14630 | 609076 |
ID: 80173 | intraflagellar transport 74 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (26947110..27066134) | BBS22, CCDC2, CMG-1, CMG1, JBTS40, SPGF58 | 608040 |
ID: 57696 | DEAD-box helicase 55 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123602099..123620943) | | 620176 |
ID: 79581 | solute carrier family 52 member 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144358552..144361272) | BVVLS2, D15Ertd747e, GPCR41, GPR172A, HuPAR-1, PAR1, RFT3, RFVT2, hRFT3 | 607882 |
ID: 30844 | EH domain containing 4 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (41895933..41972557, complement) | PAST4 | 605892 |
ID: 10785 | WD repeat domain 4 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (42843094..42892998, complement) | GAMOS6, MIGSB, TRM82, TRMT82, Wuho, hWH | 605924 |
ID: 84895 | mitoguardin 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (129036626..129072082) | C9orf54, FAM73B | 616774 |
ID: 10807 | endosome associated trafficking regulator 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (136401922..136410614, complement) | NY-CO-3, SDCCAG3, SDDAG3 | 618289 |
ID: 79039 | DEAD-box helicase 54 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (113157173..113185478, complement) | DP97 | 611665 |