ID: 80179 | myosin XIX [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (36495636..36544815, complement) | MYOHD1 | 617379 |
ID: 284098 | phosphatidylinositol glycan anchor biosynthesis class W [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (36534987..36539303) | Gwt1, HPMRS5 | 610275 |
ID: 11267 | SNF8 subunit of ESCRT-II [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (48929316..48944842, complement) | DEE115, Dot3, EAP30, NEDOA, VPS22 | 610904 |
ID: 8625 | regulatory factor X associated ankyrin containing protein [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (19192258..19201866) | ANKRA1, BLS, F14150_1, MHC2D2, RFX-B | 603200 |
ID: 257415 | family with sequence similarity 133 member B [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92560758..92590390, complement) | | |
ID: 7050 | TGFB induced factor homeobox 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (3412009..3459978) | HPE4, TGIF | 602630 |
ID: 10467 | zinc finger HIT-type containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (101218165..101224190) | CG1I, ZNFN4A1, p18(Hamlet) | 618617 |
ID: 1656 | DEAD-box helicase 6 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (118747763..118791744, complement) | HLR2, IDDILF, P54, RCK, Rck/p54 | 600326 |
ID: 127687 | chromosome 1 open reading frame 122 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37807790..37809454) | ALAESM | |
ID: 7918 | G-patch domain and ankyrin repeats 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31661228..31666283, complement) | ANKRD59, BAT4, D6S54E, G5, GPATCH10 | 142610 |
ID: 9701 | protein phosphatase 6 regulatory subunit 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (50330774..50445090) | KIAA0685, PP6R2, SAP190, SAPS2 | 610877 |
ID: 84851 | tripartite motif containing 52 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (181249062..181261143, complement) | RNF102 | 619265 |
ID: 55346 | t-complex 11 like 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (33039572..33073563) | dJ85M6.3 | |
ID: 64282 | terminal nucleotidyltransferase 4B [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (50152911..50235310) | PAPD5, TRF4-2, TUT3 | 605540 |