ID: 63905 | mannosidase beta like [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (37289655..37317260) | | |
ID: 2908 | nuclear receptor subfamily 3 group C member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (143277931..143435512, complement) | GCCR, GCR, GCRST, GR, GRL | 138040 |
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: 79001 | vitamin K epoxide reductase complex subunit 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (31090854..31094797, complement) | EDTP308, MST134, MST576, VKCFD2, VKOR | 608547 |
ID: 29110 | TANK binding kinase 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (64452120..64502114) | AIARV, FTDALS4, IIAE8, NAK, T2K | 604834 |
ID: 773 | calcium voltage-gated channel subunit alpha1 A [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (13206442..13506479, complement) | APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2, EIEE42, FHM, HPCA, MHP, MHP1, SCA6 | 601011 |
ID: 821 | calnexin [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (179678656..179731641) | CNX, IP90, P90 | 114217 |
ID: 6277 | S100 calcium binding protein A6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (153534599..153535991, complement) | 2A9, 5B10, CABP, CACY, PRA, S10A6 | 114110 |
ID: 29979 | ubiquilin 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (83659968..83707958, complement) | DA41, DSK2, PLIC-1, UBQN, XDRP1 | 605046 |
ID: 25818 | kallikrein related peptidase 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50943303..50953038, complement) | KLK-L2, KLKL2, SCTE | 605643 |
ID: 7009 | transmembrane BAX inhibitor motif containing 6 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49741557..49764934) | BAXI1, BI-1, TEGT | 600748 |
ID: 57120 | golgi associated PDZ and coiled-coil motif containing [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (117560269..117602511, complement) | CAL, FIG1, PIST, dJ94G16.2, GOPC | 606845 |
ID: 6809 | syntaxin 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (59754188..59805878) | DIAR12, MVID2, RDMVIDA, STX3 | 600876 |
ID: 54708 | membrane associated ring-CH-type finger 5 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92291167..92353964) | MARCH-V, MARCH5, MITOL, RNF153 | 610637 |
ID: 57003 | coiled-coil domain containing 47 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (63745255..63773597, complement) | GK001, MSTP041, THNS | 618260 |
ID: 10490 | vesicle transport through interaction with t-SNAREs 1B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67647085..67674632, complement) | VTI1, VTI1-LIKE, VTI1L, VTI2, v-SNARE, vti1-rp1 | 603207 |
ID: 55334 | solute carrier family 39 member 9 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (69398384..69462390) | ZIP-9, ZIP9 | 619116 |
ID: 57130 | ATPase 13A1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (19645198..19663676, complement) | ATP13A, CGI-152 | 619118 |
ID: 5281 | phosphatidylinositol glycan anchor biosynthesis class F [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (46580937..46617041, complement) | OORS | 600153 |
ID: 9526 | mannose-P-dolichol utilization defect 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (7583647..7588212) | CDGIF, HBEBP2BPA, Lec35, My008, PP3958, PQLC5, SL15, SLC66A5 | 604041 |