ID: 10730 | YME1 like 1 ATPase [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (27110111..27154384, complement) | FTSH, MEG4, OPA11, PAMP, YME1L | 607472 |
ID: 22882 | zinc fingers and homeoboxes 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (122780379..122974510) | AFR1, RAF | 609185 |
ID: 401505 | translocase of outer mitochondrial membrane 5 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (37588413..37592597, complement) | C9orf105, Tom5, bA613M10.3 | 616169 |
ID: 6136 | ribosomal protein L12 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127447674..127451406, complement) | L12, uL11 | 180475 |
ID: 84945 | abhydrolase domain containing 13 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (108218392..108234243) | BEM46L1, C13orf6, bA153I24.2 | |
ID: 90678 | leucine rich repeat and sterile alpha motif containing 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (127451486..127503501) | CMT2P, RIFLE, TAL | 610933 |
ID: 3981 | DNA ligase 4 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (108207442..108218349, complement) | LIG4S | 601837 |
ID: 54993 | zinc finger and SCAN domain containing 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (84601009..84623716) | ZFP29, ZNF854 | |
ID: 25911 | deleted in primary ciliary dyskinesia homolog (mouse) [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (101588321..101609662) | | 616467 |
ID: 25875 | LETM1 domain containing 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (51048220..51068958) | 1110019O13Rik, HCCR, HCCR-1, HCCR-2, HCCR1, HCCR2, HCRR-2, SLC55A3 | 619070 |
ID: 10558 | serine palmitoyltransferase long chain base subunit 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (92031147..92115413, complement) | ALS27, HSAN1, HSN1, LBC1, LCB1, SPT1, SPTI | 605712 |
ID: 26276 | VPS33B late endosome and lysosome associated [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90998416..91022621, complement) | KDIDAR, PFIC12 | 608552 |
ID: 51010 | exosome component 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (37779714..37785092, complement) | CGI-102, PCH1B, RRP40, Rrp40p, bA3J10.7, hRrp-40, p10 | 606489 |
ID: 29105 | cilia and flagella associated protein 20 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (58113592..58129381, complement) | BUG22, C16orf80, EVORF, GTL3, fSAP23 | 617906 |
ID: 9958 | ubiquitin specific peptidase 15 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (62260404..62416389) | UNPH-2, UNPH4 | 604731 |
ID: 27343 | DNA polymerase lambda [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (101578882..101588270, complement) | BETAN, POLKAPPA | 606343 |
ID: 84305 | PYM homolog 1, exon junction complex associated factor [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55901413..55927894, complement) | PYM, WIBG | 619753 |
ID: 10428 | craniofacial development protein 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (75293710..75433503, complement) | BCNT, BUCENTAUR, CENP-29, CP27, SWC5, Yeti, p97 | 608108 |
ID: 9321 | thyroid hormone receptor interactor 11 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (91965991..92040059, complement) | ACG1A, CEV14, GMAP-210, GMAP210, ODCD, ODCD1, TRIP-11, TRIP230 | 604505 |
ID: 83892 | potassium channel tetramerization domain containing 10 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (109448655..109477300, complement) | BTBD28, MSTP028, ULRO61, hBACURD3 | 613421 |