ID: 51103 | NADH:ubiquinone oxidoreductase complex assembly factor 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (41387353..41403026, complement) | CGI-65, CGI65, CIA30, MC1DN11 | 606934 |
ID: 197131 | ubiquitin protein ligase E3 component n-recognin 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (42942897..43106038, complement) | JBS | 605981 |
ID: 9726 | zinc finger protein 646 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (31072687..31084196) | | 619299 |
ID: 6049 | ring finger protein 6 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (26132115..26223085, complement) | | 604242 |
ID: 26276 | VPS33B late endosome and lysosome associated [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90998416..91022621, complement) | KDIDAR, PFIC12 | 608552 |
ID: 54801 | HAUS augmin like complex subunit 6 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (19053141..19102904, complement) | Dgt6, FAM29A | 613433 |
ID: 116224 | PP2A Aalpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (68780065..68785566) | C9orf42, FAM122A | 617249 |
ID: 6830 | SPT6 homolog, histone chaperone and transcription elongation factor [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28662205..28702679) | SPT6, SPT6H, emb-5 | 601333 |
ID: 145389 | solute carrier family 38 member 6 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (60981245..61083733) | NAT-1, SNAT6 | 616518 |
ID: 57570 | tRNA methyltransferase 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (60971441..60981690, complement) | COXPD26, KIAA1393, PNSED, TRM5 | 611023 |
ID: 8533 | COP9 signalosome subunit 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (17246616..17281246, complement) | CSN3, SGN3 | 604665 |
ID: 6388 | stromal cell derived factor 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28648346..28662194, complement) | | 602934 |
ID: 10445 | microspherule protein 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (49558299..49568142, complement) | ICP22BP, INO80Q, MCRS2, MSP58, P78 | 609504 |
ID: 585 | Bardet-Biedl syndrome 4 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (72686207..72738473) | | 600374 |
ID: 2553 | GA binding protein transcription factor subunit beta 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (50275389..50355198, complement) | BABPB2, E4TF1, E4TF1-47, E4TF1-53, E4TF1B, GABPB, GABPB-1, GABPB2, NRF2B1, NRF2B2 | 600610 |
ID: 80195 | transmembrane protein 254 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (80078665..80092551) | C10orf57, bA369J21.6 | |
ID: 9692 | protein only RNase P catalytic subunit [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (35121839..35277622) | COXPD54, KIAA0391, MRPP3 | 609947 |
ID: 26995 | TruB pseudouridine synthase family member 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128305159..128322447, complement) | CLONE24922 | 610727 |
ID: 6156 | ribosomal protein L30 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (98041721..98045545, complement) | L30, eL30 | 180467 |
ID: 54989 | zinc finger protein 770 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (34978341..34988287, complement) | PRO1914 | |