ID: 201255 | leucine rich repeat containing 45 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (82023305..82031151) | | |
ID: 6286 | S100 calcium binding protein P [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (6693878..6697170) | MIG9 | 600614 |
ID: 309 | annexin A6 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (151100706..151157779, complement) | ANX6, CBP68, CPB-II, p68, p70 | 114070 |
ID: 26586 | cytoskeleton associated protein 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (52455478..52476627) | LB1, TMAP, se20-10 | 611569 |
ID: 211 | 5'-aminolevulinate synthase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (52198083..52214327) | ALAS, ALAS-H, ALAS3, ALASH, MIG4 | 125290 |
ID: 6757 | SSX family member 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (52696896..52707227, complement) | CT5.2, CT5.2A, HD21, HOM-MEL-40, SSX | 300192 |
ID: 56924 | p21 (RAC1) activated kinase 6 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (40239063..40277487) | PAK5 | 608110 |
ID: 4163 | MCC regulator of WNT signaling pathway [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (113022106..113488453, complement) | MCC1 | 159350 |
ID: 57215 | THAP domain containing 11 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (67842320..67844195) | CTG-B43a, CTG-B45d, HRIHFB2206, MAHCL, RONIN, SCA51 | 609119 |
ID: 7378 | uridine phosphorylase 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (48088704..48108736) | UDRPASE, UP, UPASE, UPP | 191730 |
ID: 23390 | zinc finger DHHC-type palmitoyltransferase 17 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (76764115..76853701) | DHHC-17, DHHC17, HIP14, HIP3, HSPC294, HYPH | 607799 |
ID: 11043 | midline 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (107825735..107931637) | FXY2, MRX101, RNF60, TRIM1, XLID101 | 300204 |
ID: 132320 | sodium channel and clathrin linker 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (128873241..129093539, complement) | CAP-1A, CAP1A | 611399 |
ID: 56341 | protein arginine methyltransferase 8 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (3381349..3593973) | HRMT1L3, HRMT1L4 | 610086 |
ID: 79036 | KxDL motif containing 1 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (18557870..18569378) | BORCS4, C10orf50, C19orf50, KXDL, MST096, MSTP096 | 615178 |
ID: 727837 | SSX family member 2B [Homo sapiens (human)] | Chromosome X, NC_000023.11 (52751252..52761536) | CT5.2, CT5.2b, HOM-MEL-40, SSX | |
ID: 155038 | GTPase, IMAP family member 8 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (150450630..150479393) | IAN-9, IAN6, IAN9, IANT | 616962 |
ID: 25763 | H2A.P histone [Homo sapiens (human)] | Chromosome X, NC_000023.11 (37990779..37991314) | CXorf27, HIP17, HYPM | |
ID: 280658 | SSX family member 7 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (52644061..52654900, complement) | | 300542 |
ID: 220388 | coiled-coil domain containing 89 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (85683848..85686195, complement) | | |