ID: 23158 | TBC1 domain family member 9 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (140620782..140756385, complement) | GRAMD9, MDR1 | 618035 |
ID: 4430 | myosin IB [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (191245404..191425386) | MMI-alpha, MMIa, MYH-1c, myr1 | 606537 |
ID: 7004 | TEA domain transcription factor 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (2959397..3040676) | EFTR-2, RTEF1, TCF13L1, TEF-3, TEF3, TEFR-1, hRTEF-1B | 601714 |
ID: 2260 | fibroblast growth factor receptor 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (38411143..38468635, complement) | BFGFR, CD331, CEK, ECCL, FGFBR, FGFR-1, FLG, FLT-2, FLT2, HBGFR, HH2, HRTFDS, KAL2, N-SAM, OGD, bFGF-R-1 | 136350 |
ID: 2619 | growth arrest specific 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86944362..86947506, complement) | | 139185 |
ID: 9580 | SRY-box transcription factor 13 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (204073115..204127743) | ICA12, Sox-13 | 604748 |
ID: 23516 | solute carrier family 39 member 14 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (22367278..22434129) | HCIN, HMNDYT2, LZT-Hs4, NET34, ZIP14, cig19 | 608736 |
ID: 1981 | eukaryotic translation initiation factor 4 gamma 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (184314606..184335358) | EIF-4G1, EIF4F, EIF4G, EIF4GI, P220, PARK18 | 600495 |
ID: 100526783 | ARPIN-AP3S2 readthrough [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89830599..89912952, complement) | ARPIN, C15orf38, C15orf38-AP3S2 | |
ID: 348110 | actin related protein 2/3 complex inhibitor [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (89895006..89912952, complement) | C15orf38 | 615543 |
ID: 59277 | netrin 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95657807..95791155, complement) | PRO3091 | 610401 |
ID: 140735 | dynein light chain LC8-type 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (58083419..58095542) | DNCL1B, Dlc2, RSPH22 | 608942 |
ID: 9322 | thyroid hormone receptor interactor 10 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (6739680..6751530) | CIP4, HSTP, STOT, STP, TRIP-10 | 604504 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 2036 | erythrocyte membrane protein band 4.1 like 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (36091414..36232799) | 4.1N, MRD11 | 602879 |
ID: 26033 | attractin like 1 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (115093365..115948999) | ALP, bA338L11.1, bA454H24.1 | 612869 |
ID: 51126 | N-alpha-acetyltransferase 20, NatB catalytic subunit [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (20017290..20033655) | MRT73, NAT3, NAT3P, NAT5, NAT5P, dJ1002M8.1 | 610833 |
ID: 23176 | septin 8 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (132750819..132780083, complement) | SEP2, SEPT8, Septin-8 | 608418 |
ID: 132430 | poly(A) binding protein cytoplasmic 4 like [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (133948459..134201901, complement) | | |
ID: 10979 | FERM domain containing kindlin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (52857273..52951050, complement) | KIND2, MIG2, PLEKHC1, UNC112, UNC112B, mig-2 | 607746 |