ID: 26748 | G antigen 12I [Homo sapiens (human)] | | AL4, CT4.7, GAGE-7B, GAGE7B | 300637 |
ID: 9071 | claudin 10 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95433755..95579759) | CPETRL3, HELIX, OSP-L, OSPL | 617579 |
ID: 134288 | transmembrane protein 174 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (73173193..73175143) | | 614909 |
ID: 84141 | eva-1 homolog A, regulator of programmed cell death [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (75492318..75569719, complement) | FAM176A, TMEM166 | 618990 |
ID: 9476 | napsin A aspartic peptidase [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50358477..50365639, complement) | KAP, Kdap, NAP1, NAPA, SNAPA | 605631 |
ID: 3233 | homeobox D4 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (176151550..176153226) | HHO.C13, HOX-5.1, HOX4, HOX4B, Hox-4.2 | 142981 |
ID: 6540 | solute carrier family 6 member 13 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (220622..262836, complement) | GAT-2, GAT2, GAT3 | 615097 |
ID: 8029 | cubilin [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (16823966..17129811, complement) | IFCR, IGS, IGS1, MGA1, gp280 | 602997 |
ID: 9376 | solute carrier family 22 member 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (62992824..63015841, complement) | OAT3 | 607581 |
ID: 80333 | potassium voltage-gated channel interacting protein 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (20728606..21948772, complement) | CALP, KCHIP4 | 608182 |
ID: 6569 | solute carrier family 34 member 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (177384434..177398848) | FRTS2, HCINF2, NAPI-3, NPHLOP1, NPT2, NPTIIa, SLC11, SLC17A2 | 182309 |
ID: 9390 | solute carrier family 22 member 13 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (38265812..38278757) | OAT10, OCTL1, OCTL3, ORCTL-3, ORCTL3 | 604047 |
ID: 22797 | transcription factor EC [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (115935152..116159896, complement) | TCFEC, TFE-C-L, TFECL, bHLHe34, hTFEC-L, TFEC | 604732 |
ID: 2326 | flavin containing dimethylaniline monoxygenase 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (171248494..171285978) | | 136130 |
ID: 50617 | ATPase H+ transporting V0 subunit a4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (138706294..138798196, complement) | A4, ATP6N1B, ATP6N2, DRTA3, RDRTA2, RTA1C, RTADR, STV1, VPH1, VPP2 | 605239 |
ID: 283238 | solute carrier family 22 member 24 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (63079940..63144221, complement) | NET46 | 611698 |
ID: 3758 | potassium inwardly rectifying channel subfamily J member 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (128838020..128867296, complement) | KIR1.1, ROMK, ROMK1 | 600359 |
ID: 285848 | patatin like phospholipase domain containing 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (36243168..36313955) | ARCI10, dJ50J22.1 | 612121 |
ID: 7849 | paired box 8 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (113215997..113278921, complement) | PAX-8 | 167415 |
ID: 7809 | barttin CLCNK type accessory subunit beta [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (54998933..55017172) | BART, DFNB73 | 606412 |