ID: 4147 | matrilin 2 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (97869064..98036724) | | 602108 |
ID: 387804 | V-set and transmembrane domain containing 5 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (93818232..93850618, complement) | C11orf90 | |
ID: 283659 | protogenin [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (55611544..55743152, complement) | IGDCC5 | 613261 |
ID: 2245 | FYVE, RhoGEF and PH domain containing 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (54445454..54496234, complement) | AAS, FGDY, MRXS16, ZFYVE3 | 300546 |
ID: 4356 | MAGUK p55 scaffold protein 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (43800811..43833146, complement) | DLG3 | 601114 |
ID: 113235 | solute carrier family 46 member 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (28394642..28406592, complement) | G21, HCP1, HsPCFT, PCFT, hPCFT | 611672 |
ID: 10217 | CTD small phosphatase like [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (37861880..37984469) | C3orf8, HYA22, PSR1, RBSP3, SCP3 | 608592 |
ID: 6608 | smoothened, frizzled class receptor [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (129188633..129213545) | CRJS, FZD11, Gx, PHLSH, SMO | 601500 |
ID: 11248 | neurexophilin 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (49575871..49583827) | NPH3 | 604636 |
ID: 220963 | solute carrier family 16 member 9 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (59650764..59710079, complement) | C10orf36, MCT9 | 614242 |
ID: 161742 | sprouty related EVH1 domain containing 1 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (38252836..38357249) | LGSS, NFLS, PPP1R147, hSpred1, spred-1 | 609291 |
ID: 64283 | Rho guanine nucleotide exchange factor 28 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (73626196..73941990) | RGNEF, RIP2, p190RHOGEF | 612790 |
ID: 9495 | A-kinase anchoring protein 5 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (64465499..64474503) | AKAP75, AKAP79, H21 | 604688 |
ID: 9882 | TBC1 domain family member 4 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (75283503..75482169, complement) | AS160, NIDDM5 | 612465 |
ID: 50810 | HDGF like 3 [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (83112738..83207823, complement) | CGI-142, HDGF-2, HDGF2, HDGFRP3, HRP-3 | 616643 |
ID: 389136 | vestigial like family member 3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (86937973..86991149, complement) | VGL-3, VGL3 | 609980 |
ID: 387882 | chromosome 12 open reading frame 75 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (105330691..105371518) | AGD3, OCC-1, OCC1 | |
ID: 25814 | ataxin 10 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (45671834..45845307) | ATX10, E46L, HUMEEP, SCA10 | 611150 |
ID: 80303 | EF-hand domain family member D1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (232606057..232682776) | MST133, MSTP133, PP3051, SWS2 | 611617 |
ID: 1188 | chloride voltage-gated channel Kb [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16043782..16057326) | CLCKB, ClC-K2, ClC-Kb | 602023 |