ID: 134826889 | SPESP1-NOX5 readthrough [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (68930525..69062762) | | |
ID: 111089941 | MMP24-AS1-EDEM2 readthrough [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (35115364..35278122, complement) | | |
ID: 110599583 | EEF1AKMT4-ECE2 readthrough [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184249672..184293031) | ECE-2, ECE2 | |
ID: 105372990 | uncharacterized LOC105372990 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (30432686..30436501) | | |
ID: 100861548 | PINK1 antisense RNA [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (20642657..20652193, complement) | NAPINK11, PINK1AS, PINK1-AS | |
ID: 100533195 | FAM24B-CUZD1 readthrough [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (122832155..122879641, complement) | CUZD1 | |
ID: 100506742 | caspase 12 (gene/pseudogene) [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (104883286..104898460, complement) | CASP-12P1, CASP12 | 608633 |
ID: 100303755 | PET117 cytochrome c oxidase chaperone [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (18137863..18143169) | CSRP2BP, MC4DN19 | 614771 |
ID: 100141515 | chromosome 17 open reading frame 99 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78145571..78166297) | IL-40, UNQ464 | |
ID: 100131943 | uncharacterized LOC100131943 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (20055298..20056829) | | |
ID: 100131439 | CD300 molecule like family member d [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (74578643..74592283, complement) | CD300D, CLM-4, CLM-5, CMRF35-A4, CMRF35A4 | 616301 |
ID: 100130733 | leucine rich repeat containing 70 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (62578819..62581446) | SLRN | |
ID: 100129066 | long intergenic non-protein coding RNA 3062 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (89639783..89719759) | | |
ID: 790955 | ubiquinol-cytochrome c reductase complex assembly factor 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62671673..62673686) | C11orf83, CCDS41658.1, MC3DN9, UNQ655 | 616097 |
ID: 729201 | sperm acrosome associated 5B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (48130626..48132620) | LYZL5B | |
ID: 728276 | C-type lectin domain containing 19A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (19285731..19310947) | | |
ID: 653519 | G protein-coupled receptor 89A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (145607988..145670650) | GPHR, GPR89, GPR89B, SH120, UNQ192 | 612821 |
ID: 646962 | histidine rich carboxyl terminus 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35906202..35907136) | LGLL338, PRO537, UNQ338 | |
ID: 646627 | LY6/PLAUR domain containing 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (248739415..248755759, complement) | | 617067 |
ID: 645843 | transmembrane protein 14E, pseudogene [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (152339698..152340990, complement) | TMEM14E | |