ID: 11120 | butyrophilin subfamily 2 member A1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (26457955..26476622) | BK14H9.1, BT2.1, BTF1, BTN2.1, DJ3E1.1 | 613590 |
ID: 10051 | structural maintenance of chromosomes 4 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (160399650..160434953) | CAP-C, CAPC, SMC-4L1, SMC4 | 605575 |
ID: 26268 | F-box protein 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (53064998..53100873) | FBX9, NY-REN-57, VCIA1, dJ341E18.2 | 609091 |
ID: 57560 | intraflagellar transport 80 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (160256986..160399225, complement) | ATD2, CFAP167, FAP167, SRTD2, WDR56 | 611177 |
ID: 5890 | RAD51 paralog B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67819779..68683096) | R51H2, RAD51L1, REC2 | 602948 |
ID: 7769 | zinc finger protein 226 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (44165100..44199490) | | |
ID: 57679 | alsin Rho guanine nucleotide exchange factor ALS2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (201700267..201780933, complement) | ALS2CR6, ALSJ, IAHSP, PLSJ | 606352 |
ID: 100534599 | ISY1-RAB43 readthrough [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (129087572..129161063, complement) | ISY1 | |
ID: 57461 | ISY1 splicing factor homolog [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (129127415..129161063, complement) | FSAP33 | 612764 |
ID: 84317 | coiled-coil domain containing 115 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (130337933..130342681, complement) | CDG2O, ccp1 | 613734 |
ID: 10902 | bromodomain containing 8 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (138139770..138178630, complement) | SMAP, SMAP2, p120 | 602848 |
ID: 9277 | WD repeat domain 46 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (33279108..33289239, complement) | BING4, C6orf11, FP221, UTP7 | 611440 |
ID: 55702 | YJU2 splicing factor homolog [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (4247080..4269088) | CCDC94 | |
ID: 4836 | N-myristoyltransferase 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45061317..45109016) | HsNMT1, NMT | 160993 |
ID: 51398 | WD repeat domain 83 opposite strand [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (12668073..12669415, complement) | ASTERIX, C19orf56, NEDFHCA, PAT-10, PAT10, PTD008 | 618474 |
ID: 8726 | embryonic ectoderm development [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (86244753..86287615) | COGIS, HEED, WAIT1 | 605984 |
ID: 55759 | WD repeat domain 12 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (202874261..202911673, complement) | YTM1 | 616620 |
ID: 57697 | FA complementation group M [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (45135930..45200890) | FAAP250, KIAA1596, POF15, SPGF28 | 609644 |
ID: 55298 | ring finger protein 121 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (71929046..71997597) | | 620529 |
ID: 64598 | motile sperm domain containing 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100612162..100615377) | CDS3, NET30 | 609125 |