ID: 64949 | mitochondrial ribosomal protein S26 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3046052..3048250) | C20orf193, GI008, MRP-S13, MRP-S26, MRPS13, NY-BR-87, RPMS13, dJ534B8.3, mS26 | 611988 |
ID: 150678 | COP9 signalosome subunit 9 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (240126548..240136347, complement) | CSNAP, MYEOV2 | 619349 |
ID: 10459 | mitotic arrest deficient 2 like 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (11674480..11691830, complement) | FANCV, MAD2B, POLZ2, REV7 | 604094 |
ID: 84105 | pterin-4 alpha-carbinolamine dehydratase 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (134905131..134962644) | DCOH2, DCOHM, PHS2 | 609836 |
ID: 55262 | trafficking protein particle complex subunit 14 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100154423..100158723, complement) | C7orf43, MAP11, MCPH25 | 618350 |
ID: 8526 | diacylglycerol kinase epsilon [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56834151..56869567) | AHUS7, DAGK5, DAGK6, DGK, NPHS7 | 601440 |
ID: 199870 | family with sequence similarity 76 member A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27725961..27763116) | | |
ID: 51720 | ubiquitin interaction motif containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176905005..177022602, complement) | RAP80, X2HRIP110 | 609433 |
ID: 55571 | CCR4-NOT transcription complex subunit 11 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (101252886..101270316) | C2orf29, C40 | 620509 |
ID: 85359 | DiGeorge syndrome critical region gene 6 like [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20314238..20320060, complement) | DGCR6 | 609459 |
ID: 9816 | URB2 ribosome biogenesis homolog [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (229626247..229660200) | KIAA0133, NET10, NPA2 | 619372 |
ID: 8565 | tyrosyl-tRNA synthetase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (32775239..32817358, complement) | CMTDIC, IMNEPD2, TYRRS, YARS, YRS, YTS | 603623 |
ID: 130026 | islet cell autoantigen 1 like [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (202773176..202871766, complement) | ALS2CR14, ALS2CR15 | |
ID: 203069 | R3H domain and coiled-coil containing 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23288092..23296279) | | |
ID: 435 | argininosuccinate lyase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (66075819..66093576) | ASAL | 608310 |
ID: 376497 | solute carrier family 27 member 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17468767..17506168) | ACSVL5, FATP, FATP-1, FATP1 | 600691 |
ID: 2033 | E1A binding protein p300 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (41092592..41180077) | KAT3B, MKHK2, RSTS2, p300 | 602700 |
ID: 152519 | NIPA like domain containing 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (48016772..48040173) | NIPA3, NPAL1, SLC57A3 | 620340 |
ID: 80025 | pantothenate kinase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3888781..3929887) | C20orf48, HARP, HSS, NBIA1, PKAN | 606157 |
ID: 57045 | twisted gastrulation BMP signaling modulator 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (9334773..9402420) | TSG | 605049 |