ID: 10165 | solute carrier family 25 member 13 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96120220..96322098, complement) | ARALAR2, CITRIN, CTLN2, NICCD | 603859 |
ID: 8526 | diacylglycerol kinase epsilon [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56834151..56869567) | AHUS7, DAGK5, DAGK6, DGK, NPHS7 | 601440 |
ID: 55262 | trafficking protein particle complex subunit 14 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100154423..100158723, complement) | C7orf43, MAP11, MCPH25 | 618350 |
ID: 64834 | ELOVL fatty acid elongase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43363401..43368011, complement) | CGI-88, IKSHD, Ssc1 | 611813 |
ID: 51720 | ubiquitin interaction motif containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (176905005..177022602, complement) | RAP80, X2HRIP110 | 609433 |
ID: 9817 | kelch like ECH associated protein 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10486125..10503356, complement) | INrf2, KLHL19 | 606016 |
ID: 55722 | centrosomal protein 72 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (612340..676616) | | 616475 |
ID: 9489 | phosphatidylglycerophosphate synthase 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (78378649..78424659) | | 614942 |
ID: 8567 | MAP kinase activating death domain [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (47269188..47330031) | DEEAH, DENN, IG20, NEDDISH, RAB3GEP, RabGEF | 603584 |
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: 23288 | IQ motif containing E [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (2558979..2614728) | 1700028P05Rik, PAPA7 | 617631 |
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: 2288 | FKBP prolyl isomerase 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2794970..2805423) | FKBP51, FKBP52, FKBP59, HBI, Hsp56, PPIase, p52 | 600611 |
ID: 51629 | solute carrier family 25 member 39 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (44319628..44324823, complement) | CGI-69, CGI69 | 610820 |
ID: 220359 | tigger transposable element derived 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65354751..65357613) | | 619084 |
ID: 151194 | methyltransferase 21A, HSPA lysine [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (207580635..207626053, complement) | FAM119A, HCA557b, HSPA-KMT | 615257 |
ID: 140825 | neuralized E3 ubiquitin protein ligase 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (45888634..45891208, complement) | C20orf163, OZZ, OZZ-E3 | 608597 |
ID: 51742 | AT-rich interaction domain 4B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (235166902..235328179, complement) | BCAA, BRCAA1, RBBP1L1, RBP1L1, SAP180 | 609696 |
ID: 162 | adaptor related protein complex 1 subunit beta 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29327680..29388570, complement) | ADTB1, AP105A, BAM22, CLAPB2, KIDAR | 600157 |
ID: 84105 | pterin-4 alpha-carbinolamine dehydratase 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (134905131..134962644) | DCOH2, DCOHM, PHS2 | 609836 |