ID: 10743 | retinoic acid induced 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17681458..17811453) | SMCR, SMS | 607642 |
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: 23446 | solute carrier family 44 member 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (105244651..105438504) | CD92, CDW92, CHTL1, CONATOC, CTL1 | 606105 |
ID: 6477 | siah E3 ubiquitin protein ligase 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (48360531..48387246, complement) | BURHASA, SIAH1 | 602212 |
ID: 22856 | chondroitin sulfate synthase 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (101175727..101252048, complement) | CHSY, CSS1, ChSy-1, TPBS | 608183 |
ID: 54462 | coiled-coil serine rich protein 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (84328589..84518517) | FAM190B, Gcap14, KIAA1128, bA486O22.1 | 619944 |
ID: 3297 | heat shock transcription factor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144291604..144314720) | HSTF1 | 140580 |
ID: 2782 | G protein subunit beta 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (1785286..1891087, complement) | HG2A, MDS, MRD42 | 139380 |
ID: 10048 | RAN binding protein 9 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (13621498..13711835, complement) | BPM-L, BPM90, RANBPM, RanBP7 | 603854 |
ID: 195827 | peroxiredoxin like 2C [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (96639577..96655317, complement) | AAED1, C9orf21 | |
ID: 6418 | SET nuclear proto-oncogene [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128683424..128696396) | 2PP2A, I2PP2A, IGAAD, IPP2A2, MRD58, PHAPII, TAF-I, TAF-IBETA | 600960 |
ID: 51542 | VPS54 subunit of GARP complex [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (63892150..64019428, complement) | HCC8, PPP1R164, SLP-8pL, WR, hVps54L, VPS54 | 614633 |
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: 27183 | vacuolar protein sorting 4 homolog A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (69311350..69326939) | CIMDAG, SKD1, SKD1A, SKD2, VPS4, VPS4-1 | 609982 |
ID: 55690 | phosphofurin acidic cluster sorting protein 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66070272..66244744) | MRD17, SHMS | 607492 |
ID: 79038 | zinc finger FYVE-type containing 21 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (103715810..103733664) | HCVP7TP1, ZF21 | 613504 |
ID: 79180 | EF-hand domain family member D2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (15409888..15430339) | SWS1 | 616450 |
ID: 8440 | NCK adaptor protein 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (105744453..105894272) | GRB4, NCKbeta | 604930 |
ID: 3267 | ArfGAP with FG repeats 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (227472156..227561217) | HRB, RAB, RIP | 600862 |