ID: 83755 | keratin associated protein 4-12 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41123091..41124182, complement) | KAP4.12, KRTAP4.12 | |
ID: 5159 | platelet derived growth factor receptor beta [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (150113839..150155845, complement) | CD140B, IBGC4, IMF1, JTK12, KOGS, PDGFR, PDGFR-1, PDGFR1, PENTT | 173410 |
ID: 358 | aquaporin 1 (Colton blood group) [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (30911853..30925516) | AQP-CHIP, CHIP28, CO | 107776 |
ID: 1045 | caudal type homeobox 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (27960918..27969315, complement) | CDX-3/AS, CDX3, CDX2 | 600297 |
ID: 6890 | transporter 1, ATP binding cassette subfamily B member [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (32845209..32853704, complement) | ABC17, ABCB2, APT1, D6S114E, MHC1D1, PSF-1, PSF1, RING4*0102N, TAP1N, TAP1 | 170260 |
ID: 8038 | ADAM metallopeptidase domain 12 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (126012391..126388477, complement) | ADAM12-OT1, CAR10, MCMP, MCMPMltna, MLTN, MLTNA | 602714 |
ID: 8312 | axin 1 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (287440..352723, complement) | AXIN, CMDOH, PPP1R49 | 603816 |
ID: 3609 | interleukin enhancer binding factor 3 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (10654346..10692400) | CBTF, DRBF, DRBP76, MMP4, MPHOSPH4, MPP4, MPP4110, NF-AT-90, NF110, NF110b, NF90, NF90a, NF90b, NF90c, NF90ctv, NFAR, NFAR-1, NFAR-2, NFAR110, NFAR2, NFAR90, TCP110, TCP80 | 603182 |
ID: 7704 | zinc finger and BTB domain containing 16 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (114059711..114256770) | PLZF, ZNF145 | 176797 |
ID: 10253 | sprouty RTK signaling antagonist 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (80335976..80341126, complement) | IGAN3, hSPRY2 | 602466 |
ID: 10020 | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase [Homo sapiens (human)] | Chromosome 9, NC_000009.12 (36214441..36276978, complement) | DMRV, GLCNE, IBM2, NM, THC12, Uae1 | 603824 |
ID: 7051 | transglutaminase 1 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (24249114..24263177, complement) | ARCI1, ICR2, KTG, LI, LI1, TGASE, TGK | 190195 |
ID: 3087 | hematopoietically expressed homeobox [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (92689955..92695647) | HEX, HMPH, HOX11L-PEN, PRH, PRHX | 604420 |
ID: 9075 | claudin 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (106900164..106930861) | OAZON, claudin-2 | 300520 |
ID: 5359 | phospholipid scramblase 1 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (146515180..146544607, complement) | MMTRA1B | 604170 |
ID: 1407 | cryptochrome circadian regulator 1 [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (106991364..107093549, complement) | DSPD, PHLL1 | 601933 |
ID: 3198 | homeobox A1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (27092993..27096000, complement) | BSAS, HOX1, HOX1F | 142955 |
ID: 250 | alkaline phosphatase, placental [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (232378751..232382889) | ALP, ALPI, IAP, PALP, PLAP, PLAP-1 | 171800 |
ID: 6687 | SPG7 matrix AAA peptidase subunit, paraplegin [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (89508388..89557768) | CAR, CMAR, PGN, SPG5C | 602783 |
ID: 293 | solute carrier family 25 member 6 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (1386152..1392113, complement); Chromosome Y, NC_000024.10 (1386152..1392113, complement) | AAC3, ANT, ANT 2, ANT 3, ANT3, ANT3Y | 300151, 403000 |