ID: 51312 | solute carrier family 25 member 37 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23528956..23575463) | HT015, MFRN, MFRN1, MSC, MSCP, PRO1278, PRO1584, PRO2217 | 610387 |
ID: 11315 | Parkinsonism associated deglycase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (7961711..7985505) | DJ-1, DJ1, GATD2, HEL-S-67p | 602533 |
ID: 5822 | PWP2 small subunit processome component [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44107399..44131181) | EHOC-17H, UTP1, PWP2 | 601475 |
ID: 3268 | ArfGAP with FG repeats 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (100539203..100568220) | HRBL, RABR | 604019 |
ID: 79869 | cleavage and polyadenylation specific factor 7 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (61402729..61429975, complement) | CFIm59 | |
ID: 8560 | delta 4-desaturase, sphingolipid 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (224183240..224193441) | DEGS, DEGS-1, DES1, Des-1, FADS7, HLD18, MIG15, MLD | 615843 |
ID: 54503 | zinc finger DHHC-type palmitoyltransferase 13 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (19117104..19176415) | HIP14L, HIP3RP | 612815 |
ID: 374868 | ATPase phospholipid transporting 9B (putative) [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79069394..79378283) | ATPASEP, ATPIIB, HUSSY-20, NEO1L, hMMR1 | 614446 |
ID: 54467 | ankyrin repeat and IBR domain containing 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92245974..92401383) | | 620069 |
ID: 387263 | chromosome 6 open reading frame 120 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (169702126..169706360) | | 616987 |
ID: 10049 | DnaJ heat shock protein family (Hsp40) member B6 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (157337004..157417439) | DJ4, DnaJ, HHDJ1, HSJ-2, HSJ2, LGMD1D, LGMD1E, LGMDD1, MRJ, MSJ-1 | 611332 |
ID: 4705 | NADH:ubiquinone oxidoreductase subunit A10 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (239892442..240025342, complement) | CI-42KD, CI-42k, MC1DN22 | 603835 |
ID: 84188 | fatty acyl-CoA reductase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (13668668..13732346) | CSPSD, MLSTD2, PFCRD, SDR10E1 | 616107 |
ID: 55738 | ADP ribosylation factor GTPase activating protein 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63272813..63289790) | ARF1GAP, HRIHFB2281 | 608377 |
ID: 7289 | TUB like protein 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2890891..2941138) | HRCDF, TUBL3 | 604730 |
ID: 28982 | FLVCR choline and heme transporter 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (212858275..212899363) | AXPC1, FLVCR, MFSD7B, PCA, PCARP, SLC49A1 | 609144 |
ID: 754 | PTTG1 interacting protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (44849598..44873690, complement) | C21orf1, C21orf3, PBF1, PTTG1IP | 603784 |
ID: 889 | KRIT1 ankyrin repeat containing [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (92198969..92246100, complement) | CAM, CCM1 | 604214 |
ID: 8454 | cullin 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (148697756..148801110) | | 603134 |
ID: 11336 | exocyst complex component 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (443176..467290) | SEC6, SEC6L1, Sec6p | 608186 |