ID: 23352 | ubiquitin protein ligase E3 component n-recognin 4 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (19074510..19210266, complement) | RBAF600, ZUBR1, p600 | 609890 |
ID: 144097 | spindlin interactor and repressor of chromatin binding [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63813456..63827716) | C11orf84, SPIN-DOC | |
ID: 55113 | XK related 8 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27959973..27968093) | XRG8, hXkr8 | 619940 |
ID: 25793 | F-box protein 7 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (32474811..32498829) | FBX, FBX07, FBX7, PARK15, PKPS | 605648 |
ID: 339448 | chromosome 1 open reading frame 174 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (3889133..3900272, complement) | | |
ID: 8690 | JRK like [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (96390013..96393561) | HHMJG | 603211 |
ID: 64792 | intraflagellar transport 22 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101310914..101321823, complement) | CFAP9, FAP9, RABL5 | 620505 |
ID: 25771 | TBC1 domain family member 22A [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (46762650..47175699) | C22orf4, HSC79E021 | 616879 |
ID: 8565 | tyrosyl-tRNA synthetase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32775239..32817358, complement) | CMTDIC, IMNEPD2, TYRRS, YARS, YRS, YTS | 603623 |
ID: 10430 | transmembrane protein 147 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (35545626..35547526) | NEDFLPH, NIFIE14 | 613585 |
ID: 63933 | mitochondrial calcium uniporter regulator 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (13786557..13814557, complement) | C6orf79, CCDC90A, FMP32 | 616952 |
ID: 10745 | putative homeodomain transcription factor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (113696831..113759888, complement) | PHTF | 604950 |
ID: 126308 | MOB kinase activator 3A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (2071036..2096515, complement) | MOB-LAK, MOB1C, MOBKL2A, moblak | 620929 |
ID: 80025 | pantothenate kinase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3888781..3929887) | C20orf48, HARP, HSS, NBIA1, PKAN | 606157 |
ID: 23597 | acyl-CoA thioesterase 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (23701055..23743276, complement) | ACATE2, CGI-16, MT-ACT48, MTACT48 | 300862 |
ID: 85015 | ubiquitin specific peptidase 45 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (99432325..99517846, complement) | LCA19 | 618439 |
ID: 1263 | polo like kinase 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (44800377..44805990) | CNK, FNK, PLK-3, PRK | 602913 |
ID: 64224 | HERPUD family member 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (35632659..35695135, complement) | | 620829 |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |
ID: 533 | ATPase H+ transporting V0 subunit b [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43974960..43978295) | ATP6F, HATPL, VMA16 | 603717 |