ID: 59277 | netrin 4 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (95657807..95791155, complement) | PRO3091 | 610401 |
ID: 5727 | patched 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (95442980..95516971, complement) | BCNS, BCNS1, NBCCS, PTC, PTC1, PTCH | 601309 |
ID: 84952 | cingulin like 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (57376505..57550717) | JACOP, PCING | 607856 |
ID: 5738 | prostaglandin F2 receptor inhibitor [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (116909916..116990353) | CD315, CD9P-1, EWI-F, FPRP, SMAP-6 | 601204 |
ID: 23158 | TBC1 domain family member 9 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (140620782..140756385, complement) | GRAMD9, MDR1 | 618035 |
ID: 126969 | solute carrier family 44 member 3 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (94820357..94895247) | CTL3 | 620328 |
ID: 657 | bone morphogenetic protein receptor type 1A [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (86755763..86932844) | 10q23del, ACVRLK3, ALK-3, ALK3, BMPR-1A, CD292, SKR5 | 601299 |
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: 64423 | inverted formin 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104689618..104722535) | C14orf151, C14orf173, CMTDIE, FSGS5, pp9484 | 610982 |
ID: 283638 | centrosomal protein 170B [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (104864513..104896747) | CEP170R, FAM68C, KIAA0284 | 620251 |
ID: 4430 | myosin IB [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (191245404..191425386) | MMI-alpha, MMIa, MYH-1c, myr1 | 606537 |
ID: 57475 | pleckstrin homology, MyTH4 and FERM domain containing H1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (67533290..67589612) | | |
ID: 2619 | growth arrest specific 1 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (86944362..86947506, complement) | | 139185 |
ID: 5774 | protein tyrosine phosphatase non-receptor type 3 [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (109375694..109538420, complement) | PTP-H1, PTPH1 | 176877 |
ID: 23286 | WW and C2 domain containing 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (168291645..168472303) | HBEBP3, HBEBP36, KIBRA, MEMRYQTL, PPP1R168 | 610533 |
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 |
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: 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: 4891 | solute carrier family 11 member 2 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (50952263..51028886, complement) | AHMIO1, DCT1, DMT1, NRAMP2 | 600523 |
ID: 2036 | erythrocyte membrane protein band 4.1 like 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (36091414..36232799) | 4.1N, MRD11 | 602879 |