ID: 64968 | mitochondrial ribosomal protein S6 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34073578..34143030) | C21orf101, MRP-S6, RPMS6, S6mt, bS6m | 611973 |
ID: 6526 | solute carrier family 5 member 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34073578..34106260) | BCW2, SMIT, SMIT1, SMIT2 | 600444 |
ID: 90780 | pygopus family PHD finger 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (154957026..154961782, complement) | 1190004M21Rik | 606903 |
ID: 23358 | ubiquitin specific peptidase 24 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (55066359..55215364, complement) | | 610569 |
ID: 64769 | MYST/Esa1 associated factor 6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (37489993..37514766, complement) | C1orf149, CENP-28, EAF6, NY-SAR-91 | 611001 |
ID: 7532 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (76326799..76358991, complement) | 14-3-3GAMMA, DEE56, EIEE56, PPP1R170 | 605356 |
ID: 9986 | Ras converting CAAX endopeptidase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (66843441..66846552) | FACE2A, RCE1B, RCE1 | 605385 |
ID: 253260 | RPTOR independent companion of MTOR complex 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (38937920..39074399, complement) | AVO3, PIA, hAVO3 | 609022 |
ID: 7534 | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (100916523..100953382, complement) | 14-3-3-zeta, HEL-S-3, HEL-S-93, HEL4, KCIP-1, POPCHAS, YWHAD | 601288 |
ID: 64326 | COP1 E3 ubiquitin ligase [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (175944831..176207286, complement) | CFAP78, FAP78, RFWD2, RNF200 | 608067 |
ID: 84961 | F-box and leucine rich repeat protein 20 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (39252663..39402556, complement) | Fbl2, Fbl20 | 609086 |
ID: 11335 | chromobox 3 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (26201443..26213607) | HECH, HP1-GAMMA, HP1Hs-gamma, HP1gamma | 604477 |
ID: 79892 | minichromosome maintenance complex binding protein [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (119829440..119873581, complement) | C10orf119, MCM-BP | 610909 |
ID: 201595 | STT3 oligosaccharyltransferase complex catalytic subunit B [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (31532925..31637616) | CDG1X, SIMP, STT3-B | 608605 |
ID: 54014 | bromodomain and WD repeat domain containing 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39184176..39321212, complement) | C21orf107, CILD51, DCAF19, N143, WDR9, WRD9 | 617824 |
ID: 10949 | heterogeneous nuclear ribonucleoprotein A0 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (137745651..137754363, complement) | HNRPA0 | 609409 |
ID: 221710 | small integral membrane protein 13 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (11093834..11138733) | C6orf228 | |
ID: 64839 | F-box and leucine rich repeat protein 17 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (107859035..108382098, complement) | FBXO13, Fbl17, Fbx13 | 609083 |
ID: 8566 | pyridoxal kinase [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (43719129..43762299) | C21orf124, C21orf97, HEL-S-1a, HMSN6C, PKH, PNK, PRED79 | 179020 |
ID: 64225 | atlastin GTPase 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (38293954..38378584, complement) | ARL3IP2, ARL6IP2, aip-2, atlastin2 | 609368 |