ID: 644068 | ribosomal protein S14 pseudogene 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (19607807..19608644) | RPS14_1_16 | |
ID: 10381 | tubulin beta 3 class III [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89921925..89936097) | CDCBM, CDCBM1, CFEOM3, CFEOM3A, FEOM3, TUBB4, beta-4 | 602661 |
ID: 3704 | inosine triphosphatase [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (3204065..3227449) | C20orf37, DEE35, HLC14-06-P, ITPase, My049, NTPase, dJ794I6.3 | 147520 |
ID: 1001 | cadherin 3 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (68645310..68733771) | CDHP, HJMD, PCAD | 114021 |
ID: 1831 | TSC22 domain family member 3 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (107713221..107775988, complement) | DIP, DSIPI, GILZ, TSC-22R | 300506 |
ID: 119 | adducin 2 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (70656784..70768200, complement) | ADDB | 102681 |
ID: 79633 | FAT atypical cadherin 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (125314955..125492932) | CDHF14, CDHR11, FAT-J, FATJ, HKLLS2, NBLA00548, VMLDS2 | 612411 |
ID: 345651 | actin beta like 2 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (57480018..57482811, complement) | ACT | 614835 |
ID: 5119 | charged multivesicular body protein 1A [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89644435..89657708, complement) | CHMP1, PCH8, PCOLN3, PRSM1, VPS46-1, VPS46A | 164010 |
ID: 1952 | cadherin EGF LAG seven-pass G-type receptor 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (109249539..109275751) | ADGRC2, CDHF10, EGFL2, Flamingo1, MEGF3 | 604265 |
ID: 8218 | clathrin heavy chain like 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (19179473..19291719, complement) | CHC22, CLH22, CLTCL, CLTD | 601273 |
ID: 5099 | protocadherin 7 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (30720369..31146800) | BH-Pcdh, BHPCDH, PPP1R120 | 602988 |
ID: 55871 | Zn regulated GTPase metalloprotein activator 1A [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (120837..179056, complement) | CBWD1, COBP | 611078 |
ID: 120114 | FAT atypical cadherin 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (92224818..92896473) | CDHF15, CDHR10, hFat3 | 612483 |
ID: 80755 | alanyl-tRNA synthetase domain containing 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (42950526..42964454, complement) | AlaXp | 613212 |