ID: 728378 | POTE ankyrin domain family member F [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (130073535..130129222, complement) | A26C1B, ACTB, POTE2alpha, POTEACTIN | |
ID: 653437 | aquaporin 12B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (240676418..240683810, complement) | INSSA3 | |
ID: 643905 | proline rich 21 [Homo sapiens (human)] | | | |
ID: 401285 | t-complex 10 like 2 (pseudogene) [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (167170619..167196751) | | |
ID: 388759 | long intergenic non-protein coding RNA 2897 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (247110155..247112417, complement) | C1orf229 | |
ID: 121551 | ankyrin repeat and BTB domain containing 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (107318434..107659642) | ABTB2B, BTBD11 | |
ID: 116988 | ArfGAP with GTPase domain, ankyrin repeat and PH domain 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (151085867..151144434) | AGAP-3, CENTG3, CRAG, MRIP-1, cnt-g3 | 616813 |
ID: 84250 | SMC5-SMC6 complex localization factor 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (94618231..94697621) | ANKRD32, BRCTD1, BRCTx | 618467 |
ID: 55681 | SCY1 like pseudokinase 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (100267177..100341715) | AMC4, AMCNACC, CVAK104 | 616365 |
ID: 55504 | TNF receptor superfamily member 19 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (23570412..23676093) | TAJ, TAJ-alpha, TRADE, TROY | 606122 |
ID: 54754 | NUT family member 2F [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (94318198..94328644, complement) | FAM22F, NUTMF | |
ID: 9933 | pumilio RNA binding family member 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (2804152..2844095, complement) | HA-8, HLA-HA8, KIAA0020, PEN, PUF-A, PUF6, XTP5 | 609960 |
ID: 7273 | titin [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (178525989..178807423, complement) | CMD1G, CMH9, CMPD4, CMYO5, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD | 188840 |
ID: 4253 | MIA SH3 domain ER export factor 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (39233915..39388522) | CTAGE5, MEA6, MGEA, MGEA11, MGEA6, TALI | 602132 |
ID: 3768 | potassium inwardly rectifying channel subfamily J member 12 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (21376357..21419870) | IRK-2, IRK2, KCNJN1, Kir2.2, hIRK, hIRK1, hkir2.2x, kcnj12x | 602323 |
ID: 3106 | major histocompatibility complex, class I, B [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (31353875..31357179, complement) | AS, B-4901, HLAB | 142830 |