ID: 3988 | lipase A, lysosomal acid type [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (89213572..89251775, complement) | CESD, LAL | 613497 |
ID: 286148 | dpy-19 like 4 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (94719900..94793836) | | 613895 |
ID: 55275 | VPS53 subunit of GARP complex [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (508668..714839, complement) | HCCS1, PCH2E, hVps53L, pp13624 | 615850 |
ID: 51527 | GSK3B interacting protein [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96363526..96387290) | C14orf129, HSPC210 | 616605 |
ID: 23659 | phospholipase A2 group XV [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68245373..68261058) | ACS, GXVPLA2, LLPL, LPLA2, LYPLA3 | 609362 |
ID: 5095 | propionyl-CoA carboxylase subunit alpha [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (100089093..100530435) | | 232000 |
ID: 23293 | SMG6 nonsense mediated mRNA decay factor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (2059839..2303785, complement) | C17orf31, EST1A, SMG-6, hEST1A, hSMG5/7a | 610963 |
ID: 84622 | zinc finger protein 594 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (5174083..5191868, complement) | | |
ID: 81689 | iron-sulfur cluster assembly 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86264546..86282538, complement) | HBLD2, ISA1, MMDS5, hIscA, hIscA1 | 611006 |
ID: 26292 | MYC binding protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (38862490..38873378, complement) | AMY-1 | 606535 |
ID: 6386 | syndecan binding protein [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (58553261..58582858) | MDA-9, MDA91, ST1, SYCL, TACIP18, SDCBP | 602217 |
ID: 11332 | acyl-CoA thioesterase 7 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (6264272..6393767, complement) | ACH1, ACT, BACH, CTE-II, LACH, LACH1, hBACH | 602587 |
ID: 51108 | methyltransferase 9, His-X-His N1(pi)-histidine [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (21597208..21657471) | CGI-81, DREV, DREV1, PAP1, hMETTL9 | 609388 |
ID: 54677 | carnitine O-octanoyltransferase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (87345664..87399794) | COT | 606090 |
ID: 83856 | fibronectin type III and SPRY domain containing 1 like [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (105442177..105552433) | CCDC10, CSDUFD1, FSD1CL, FSD1NL, MIR1 | 609829 |
ID: 889 | KRIT1 ankyrin repeat containing [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92198969..92246100, complement) | CAM, CCM1 | 604214 |
ID: 116843 | solute carrier family 18 member B1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (132769370..132798637, complement) | C6orf192, VPAT, dJ55C23.6 | 613361 |
ID: 55102 | autophagy related 2B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (96279195..96363341, complement) | BLTP4B, C14orf103 | 616226 |
ID: 79631 | elongation factor like GTPase 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (82130233..82262734, complement) | EFTUD1, FAM42A, HsT19294, RIA1, SDS2 | 617538 |
ID: 84182 | MINDY lysine 48 deubiquitinase 4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (30771417..30892387) | AQP-1, AQP1, C7orf67, CHIP28, FAM188B | |