ID: 81624 | diaphanous related formin 3 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (59665583..60163928, complement) | AN, AUNA1, DIA2, DRF3, NSDAN, diap3, mDia2 | 614567 |
ID: 29095 | ORMDL sphingolipid biosynthesis regulator 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55818041..55821879) | HSPC160, MST095, MSTP095, adoplin-2 | 610074 |
ID: 11130 | ZW10 interacting kinetochore protein [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (56357227..56361273, complement) | HZwint-1, KNTC2AP, SIP301, ZWINT | 609177 |
ID: 80184 | centrosomal protein 290 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (88049016..88142088, complement) | 3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16 | 610142 |
ID: 23594 | origin recognition complex subunit 6 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (46689659..46698394) | ORC6L | 607213 |
ID: 160418 | transmembrane O-mannosyltransferase targeting cadherins 3 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (88142307..88199887) | LIS8, SMILE | 617218 |
ID: 9787 | DLG associated protein 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (55148135..55191585, complement) | DLG7, HURP | 617859 |
ID: 2954 | glutathione S-transferase zeta 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (77321036..77331597) | GSTZ1-1, MAAI, MAAID, MAI | 603758 |
ID: 10526 | importin 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (30628988..30695869, complement) | RANBP8, VISS | 605600 |
ID: 91574 | mitochondrial translation release factor in rescue [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (123232914..123257960) | C12orf65, COXPD7, SPG55, mtRF-R | 613541 |
ID: 9055 | protein regulator of cytokinesis 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (90966040..90994535, complement) | ASE1, MAP65 | 603484 |
ID: 5932 | RB binding protein 8, endonuclease [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (22914139..23026486) | COM1, CTIP, JAWAD, JWDS, RIM, SAE2, SCKL2 | 604124 |
ID: 55357 | TBC1 domain family member 2 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (98198998..98255649, complement) | PARIS-1, PARIS1A, TBC1D2 | 609871 |
ID: 2189 | FA complementation group G [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (35073839..35079942, complement) | FAG, XRCC9 | 602956 |