ID: 10518 | calcium and integrin binding family member 2 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (78104606..78131535, complement) | DFNB48, KIP2, USH1J | 605564 |
ID: 376497 | solute carrier family 27 member 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (17468767..17506168) | ACSVL5, FATP, FATP-1, FATP1 | 600691 |
ID: 81619 | tetraspanin 14 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (80454310..80522631) | DC-TM4F2, TM4SF14, tspan-14 | |
ID: 25792 | CDKN1A interacting zinc finger protein 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (128166065..128204222, complement) | LSFR1, NP94, ZNF356 | 611420 |
ID: 57045 | twisted gastrulation BMP signaling modulator 1 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (9334773..9402420) | TSG | 605049 |
ID: 26088 | golgi associated, gamma adaptin ear containing, ARF binding protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37608834..37633564) | | 606004 |
ID: 9827 | RGP1 homolog, RAB6A GEF complex partner 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35749287..35790428) | KIAA0258 | 615742 |
ID: 63977 | PR/SET domain 15 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41798225..41879344, complement) | C21orf83, PFM15, ZNF298 | 617692 |
ID: 6687 | SPG7 matrix AAA peptidase subunit, paraplegin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89508388..89557768) | CAR, CMAR, PGN, SPG5C | 602783 |
ID: 25831 | HECT domain E3 ubiquitin protein ligase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (31100117..31207793, complement) | EULIR | 618649 |
ID: 9094 | unc-119 lipid binding chaperone [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28546707..28552628, complement) | CORD24, HRG4, IMD13, POC7, POC7A | 604011 |
ID: 51114 | zinc finger DHHC-type palmitoyltransferase 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (129803288..129843886, complement) | CGI89, CXorf11, DHHC9, MMSA1, MRXSR, MRXSZ, ZDHHC10, ZNF379, ZNF380 | 300646 |
ID: 79850 | TLC domain containing 3A [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (732596..742968) | CT120, FAM57A | 611627 |
ID: 51125 | golgin A7 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (41490396..41510980) | GCP16, GOLGA3AP1A, HSPC041, GOLGA7 | 609453 |
ID: 57704 | glucosylceramidase beta 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35736866..35749228, complement) | AD035, NLGase, SPG46 | 609471 |
ID: 199870 | family with sequence similarity 76 member A [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (27725961..27763116) | | |
ID: 23078 | von Willebrand factor A domain containing 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (41566835..41961109, complement) | KIAA0564, P7BP2, RP97 | 617509 |
ID: 57410 | SCY1 like pseudokinase 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (65525083..65538704) | GKLP, HT019, NKTL, NTKL, P105, SCAR21, TAPK, TEIF, TRAP | 607982 |
ID: 1186 | chloride voltage-gated channel 7 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (1444935..1475028, complement) | CLC-7, CLC7, HOD, OPTA2, OPTB4, PPP1R63 | 602727 |
ID: 90956 | aarF domain containing kinase 2 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (140672945..140695110) | AARF | |