ID: 374900 | zinc finger protein 568 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (36916332..36997932) | ZFP568 | 617566 |
ID: 374899 | zinc finger protein 829 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (36888124..36916291, complement) | | |
ID: 23443 | solute carrier family 35 member A3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (99969996..100035634) | AMRS | 605632 |
ID: 54943 | DnaJ heat shock protein family (Hsp40) member C28 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33488055..33491716, complement) | C21orf55, C21orf78 | |
ID: 8539 | apoptosis inhibitor 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (43311996..43344529) | AAC-11, AAC11 | 609774 |
ID: 9648 | GRIP and coiled-coil domain containing 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (108449206..108509415) | GCC185, RANBP2L4, REN53 | 612711 |
ID: 345778 | metaxin 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (79976716..79991262, complement) | | 619336 |
ID: 10827 | family with sequence similarity 114 member A2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (153990148..154038910, complement) | 133K02, C5orf3 | |
ID: 65005 | mitochondrial ribosomal protein L9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (151759647..151763496, complement) | L9mt, bL9m | 611824 |
ID: 1207 | chloride nucleotide-sensitive channel 1A [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (77614530..77637794, complement) | CLCI, CLNS1B, ICln | 602158 |
ID: 80227 | proteasomal ATPase associated factor 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (73876699..73931114) | PAAF, Rpn14, WDR71 | 619772 |
ID: 284131 | endonuclease V [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80415167..80438086) | | 619821 |
ID: 4238 | microfibril associated protein 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (154038967..154057450) | | 600491 |
ID: 345757 | family with sequence similarity 174 member A [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (100535374..100586741) | HGS_RE408, NS5ATP6, TMEM157, UNQ1912 | |
ID: 5378 | PMS1 homolog 1, mismatch repair system component [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (189784450..189877629) | HNPCC3, MLH2, PMSL1, hPMS1 | 600258 |
ID: 57150 | small integral membrane protein 8 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (87322588..87342329) | C6orf162, dJ102H19.2 | |
ID: 8890 | eukaryotic translation initiation factor 2B subunit delta [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (27364352..27370338, complement) | EIF-2B, EIF2B, EIF2Bdelta, VWM4 | 606687 |
ID: 64789 | exonuclease 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (40508767..40516038) | C1orf176, DEM1, Exo V, hExo5 | 618601 |
ID: 6138 | ribosomal protein L15 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (23916545..23924631) | DBA12, EC45, L15, RPL10, RPLY10, RPYL10, eL15 | 604174 |
ID: 619208 | family with sequence similarity 229 member B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (112087591..112102790) | C6orf225 | |