ID: 10498 | coactivator associated arginine methyltransferase 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10871553..10923075) | PRMT4 | 603934 |
ID: 2590 | polypeptide N-acetylgalactosaminyltransferase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230057789..230282122) | CDG2T, GalNAc-T2 | 602274 |
ID: 1994 | ELAV like RNA binding protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7958573..8005641, complement) | ELAV1, HUR, Hua, MelG | 603466 |
ID: 23181 | disco interacting protein 2 homolog A [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46458891..46583871) | C21orf106, DIP2 | 607711 |
ID: 22902 | RUN and FYVE domain containing 3 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (70703767..70808619) | RIPX, SINGAR1, ZFYVE30 | 611194 |
ID: 149986 | LSM family member 14B [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (62122475..62135374) | C20orf40, FAM61B, FT005, LSM13, RAP55B, bA11M20.3 | 620689 |
ID: 56907 | spire type actin nucleation factor 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (12446512..12662091, complement) | Spir-1 | 609216 |
ID: 9139 | CBFA2/RUNX1 partner transcriptional co-repressor 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (33490096..33650030) | EHT, MTGR1, ZMYND3, p85 | 603672 |
ID: 23095 | kinesin family member 1B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (10210570..10381603) | CMT2, CMT2A, CMT2A1, HMSNII, KLP, NBLST1 | 605995 |
ID: 91404 | SEC14 and spectrin domain containing 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (179101678..179264832, complement) | Solo | 621011 |
ID: 57154 | SMAD specific E3 ubiquitin protein ligase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (99027440..99144108, complement) | | 605568 |
ID: 6597 | SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10961030..11062273) | BAF190, BAF190A, BRG1, CSS4, MRD16, OTSC12, RTPS2, SNF2, SNF2-beta, SNF2L4, SNF2LB, SWI2, hSNF2b | 603254 |
ID: 898 | cyclin E1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (29811991..29824312) | CCNE, pCCNE1 | 123837 |
ID: 11228 | Ras association domain family member 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (25958232..26079889) | C12orf2, HOJ1 | 608231 |
ID: 9486 | carbohydrate sulfotransferase 10 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100391860..100417668, complement) | HNK-1ST, HNK1ST | 606376 |
ID: 93624 | transcriptional adaptor 2B [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (7043372..7057952) | ADA2(beta), ADA2B | 608790 |
ID: 10743 | retinoic acid induced 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17681458..17811453) | SMCR, SMS | 607642 |
ID: 5797 | protein tyrosine phosphatase receptor type M [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (7567316..8406856) | PTPRL1, R-PTP-MU, RPTPM, RPTPU, hR-PTPu | 176888 |