ID: 112609 | melanocortin 2 receptor accessory protein 2 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (84033178..84146282) | C6orf117, bA51G5.2 | 615410 |
ID: 84619 | zinc finger CCCH-type and G-patch domain containing [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63707442..63736142) | GPATC6, GPATCH6, KIAA1847, ZC3H9, ZC3HDC9, ZIP | 619577 |
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: 25825 | beta-secretase 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (41168160..41282530) | AEPLC, ALP56, ASP1, ASP21, BAE2, CDA13, CEAP1, DRAP | 605668 |
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: 23158 | TBC1 domain family member 9 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (140620782..140756385, complement) | GRAMD9, MDR1 | 618035 |
ID: 6536 | solute carrier family 6 member 9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (43996483..44031462, complement) | GCENSG, GLYT1 | 601019 |
ID: 387882 | chromosome 12 open reading frame 75 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (105330691..105371518) | AGD3, OCC-1, OCC1 | |
ID: 26064 | retinoic acid induced 14 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (34656328..34832612) | NORPEG, RAI13 | 606586 |
ID: 64283 | Rho guanine nucleotide exchange factor 28 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (73626196..73941990) | RGNEF, RIP2, p190RHOGEF | 612790 |
ID: 3912 | laminin subunit beta 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (107923799..108003161, complement) | CLM, LIS5 | 150240 |
ID: 83857 | transmembrane O-mannosyltransferase targeting cadherins 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (29500813..29784759, complement) | ARG99, OLFA, TMTC1 | 615855 |
ID: 5902 | RAN binding protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (20116104..20127355) | HTF9A | 601180 |
ID: 84553 | failed axon connections homolog, metaxin like GST domain containing [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (99271161..99350056, complement) | C6orf168, dJ273F20 | |
ID: 81031 | solute carrier family 2 member 10 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (46708320..46736347) | ATORS, ATS, GLUT10 | 606145 |
ID: 389136 | vestigial like family member 3 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (86937973..86991149, complement) | VGL-3, VGL3 | 609980 |
ID: 261729 | STEAP2 metalloreductase [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (90211740..90243408) | IPCA1, PCANAP1, PUMPCn, STAMP1, STMP | 605094 |
ID: 967 | CD63 molecule [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (55723535..55730041, complement) | AD1, HOP-26, ME491, MLA1, OMA81H, Pltgp40, TSPAN30 | 155740 |
ID: 137392 | CBY1 interacting BAR domain containing 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (93700550..93731527) | BARMR1, FAM92A, FAM92A1, PAPA9 | 617273 |
ID: 9037 | semaphorin 5A [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (9035033..9546075, complement) | SEMAF, semF | 609297 |