ID: 51015 | isochorismatase domain containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (129094749..129114028) | CGI-111 | 620805 |
ID: 55830 | glycosyltransferase 8 domain containing 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (52694486..52705791, complement) | AD-017, MSTP139 | 618399 |
ID: 55300 | phosphatidylinositol 4-kinase type 2 beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (25234033..25279204) | PI4KIIB, PIK42B | 612101 |
ID: 284613 | cytochrome b561 family member D1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (109494094..109500435) | | |
ID: 4437 | mutS homolog 3 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (80654652..80876815) | DUP, FAP4, MRP1 | 600887 |
ID: 9588 | peroxiredoxin 6 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (173477335..173488815) | 1-Cys, AOP2, HEL-S-128m, LPCAT-5, NSGPx, PRX, aiPLA2, p29 | 602316 |
ID: 7266 | DnaJ heat shock protein family (Hsp40) member C7 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41976435..42017439, complement) | DJ11, DJC7, TPR2, TTC2 | 601964 |
ID: 6526 | solute carrier family 5 member 3 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34073578..34106260) | BCW2, SMIT, SMIT1, SMIT2 | 600444 |
ID: 4299 | ALF transcription elongation factor 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (86935011..87141039) | AF4, FEL, MLLT2, PBM1 | 159557 |
ID: 28969 | basic leucine zipper and W2 domains 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (16646181..16706517) | 5MP1, HSPC028, MST017, MSTP017 | 619275 |
ID: 2720 | galactosidase beta 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (32961108..33097146, complement) | EBP, ELNR1, MPS4B | 611458 |
ID: 170384 | fucosyltransferase 11 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (73772276..73780254) | FUCTXI | 616932 |
ID: 27010 | thiamin pyrophosphokinase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (144451941..144836437, complement) | HTPK1, PP20, THMD5 | 606370 |
ID: 55183 | replication timing regulatory factor 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (151409902..151534435) | | 608952 |
ID: 23358 | ubiquitin specific peptidase 24 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (55066359..55215364, complement) | | 610569 |
ID: 1314 | COPI coat complex subunit alpha [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (160288594..160343250, complement) | AIAISD, AILJK, HEP-COP, alpha-COP | 601924 |
ID: 53407 | syntaxin 18 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (4418968..4542343, complement) | Ufe1 | 606046 |
ID: 643853 | transmembrane protein with metallophosphoesterase domain [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (33090422..33097146, complement) | | |
ID: 55346 | t-complex 11 like 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (33039572..33073563) | dJ85M6.3 | |
ID: 5921 | RAS p21 protein activator 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (87267883..87391916) | CM-AVM, CMAVM, CMAVM1, GAP, PKWS, RASA, RASGAP, p120, p120GAP, p120RASGAP | 139150 |