ID: 10855 | heparanase [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (83292461..83335153, complement) | HPA, HPA1, HPR11, HSE1, HPSE | 604724 |
ID: 7786 | mitogen-activated protein kinase kinase kinase 12 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (53479669..53501539, complement) | DLK, HP09298, MEKK12, MUK, ZPK, ZPKP1 | 600447 |
ID: 10295 | branched chain keto acid dehydrogenase kinase [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (31108386..31117640) | BCKDKD, BDK | 614901 |
ID: 57761 | tribbles pseudokinase 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (380760..397559) | C20orf97, NIPK, SINK, SKIP3, TRB3 | 607898 |
ID: 220988 | heterogeneous nuclear ribonucleoprotein A3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (177212794..177223959) | 2610510D13Rik, D10S102, FBRNP, HNRPA3 | 605372 |
ID: 203054 | aarF domain containing kinase 5 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (144373088..144393242) | | |
ID: 138162 | piercer of microtubule wall 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (135495181..135499869, complement) | C9orf116, RbEST47 | 614502 |
ID: 5264 | phytanoyl-CoA 2-hydroxylase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (13277799..13300064, complement) | LN1, LNAP1, PAHX1, RD, PHYH | 602026 |
ID: 9810 | ring finger protein 40 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (30761612..30776307) | BRE1B, RBP95, STARING | 607700 |
ID: 55100 | WD repeat domain 70 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (37379318..37753435) | | 617233 |
ID: 283643 | tubulin epsilon and delta complex 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (105489855..105499248) | C14orf80 | |
ID: 56996 | solute carrier family 12 member 9 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100826869..100867012) | CCC6, CIP1, WO3.3, hCCC6 | 616861 |
ID: 10188 | tyrosine kinase non receptor 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (195863364..195908551, complement) | ACK, ACK-1, ACK1, p21cdc42Hs | 606994 |
ID: 78995 | homologous recombination factor with OB-fold [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44141930..44162476) | C17orf53, MCM8IP, ODG11 | 618611 |
ID: 10287 | regulator of G protein signaling 19 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (64073181..64079964, complement) | GAIP, RGSGAIP | 605071 |
ID: 6319 | stearoyl-CoA desaturase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (100347233..100364826) | FADS5, MSTP0081, SCDOS, hSCD1, SCD | 604031 |
ID: 92340 | proline rich 29 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (63998351..64004305) | C17orf72 | |
ID: 152007 | GLI pathogenesis related 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (36136536..36163913) | C9orf19, GAPR-1, GAPR1, gliPR 2 | 607141 |
ID: 387856 | coiled-coil domain containing 184 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (48183644..48185926) | C12orf68 | |
ID: 54958 | transmembrane protein 160 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (47045909..47048624, complement) | | 620258 |