ID: 5365 | plexin B3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153764249..153779341) | PLEXB3, PLEXR, PLXN6 | 300214 |
ID: 102723591 | PLXNB3 antisense RNA 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153758067..153766526, complement) | | |
ID: 9820 | cullin 7 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43037617..43053851, complement) | 3M1, CUL-7, KIAA0076, dJ20C7.5 | 609577 |
ID: 9863 | membrane associated guanylate kinase, WW and PDZ domain containing 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (78017055..79453667, complement) | ACVRIP1, AIP-1, AIP1, ARIP1, MAGI-2, NPHS15, SSCAM | 606382 |
ID: 9826 | Rho guanine nucleotide exchange factor 11 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (156934840..157046903, complement) | GTRAP48, PDZ-RHOGEF | 605708 |
ID: 9037 | semaphorin 5A [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (9035033..9546075, complement) | SEMAF, semF | 609297 |
ID: 6014 | Ras like without CAAX 2 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (42743227..43115685, complement) | RIBA, RIN, ROC2 | 609592 |
ID: 260425 | membrane associated guanylate kinase, WW and PDZ domain containing 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (113390515..113685923) | MAGI-3, dJ730K3.2 | 615943 |
ID: 63891 | ring finger protein 123 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (49689557..49721529) | FP1477, KPC1 | 614472 |
ID: 9806 | SPARC (osteonectin), cwcv and kazal like domains proteoglycan 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (72059034..72089032, complement) | testican-2 | 607988 |
ID: 23113 | cullin 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (43182196..43224587) | H7AP1, PARC | 607489 |
ID: 6782 | heat shock protein family A (Hsp70) member 13 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14371115..14383146, complement) | STCH | 601100 |
ID: 22903 | BTB domain containing 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (11890817..11926595) | dJ742J24.1 | 615566 |
ID: 26576 | SRSF protein kinase 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (153781041..153785730) | MSSK-1, MSSK1, STK23 | 301002 |
ID: 257203 | Down syndrome critical region 9 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (37208503..37221736) | NCRNA00038 | |