ID: 79192 | iroquois homeobox 1 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (3595832..3601403) | IRX-5, IRXA1 | 606197 |
ID: 3159 | high mobility group AT-hook 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (34236873..34246231) | HMG-RA, HMGIY, HMGA1 | 600701 |
ID: 114897 | C1q and TNF related 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (79022934..79049788) | CTRP1, GIP, ZSIG37 | 610365 |
ID: 50805 | iroquois homeobox 4 [Homo sapiens (human)] | Chromosome 5, NC_000005.10 (1877413..1887179, complement) | IRXA3 | 606199 |
ID: 122786 | FERM domain containing 6 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (51396431..51730727) | C14orf31, EX1, Willin, c14_5320 | 614555 |
ID: 84109 | pyroglutamylated RFamide peptide receptor [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (121328642..121381018, complement) | AQ27, GPR103, SP9155 | 606925 |
ID: 3861 | keratin 14 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41582279..41586895, complement) | CK14, EBS1, EBS1A, EBS1B, EBS1C, EBS1D, EBS3, EBS4, K14, NFJ | 148066 |
ID: 55287 | transmembrane protein 40 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (12733528..12769457, complement) | | |
ID: 374 | amphiregulin [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (74445136..74455005) | ARB, CRDGF, SDGF, AREG | 104640 |
ID: 3872 | keratin 17 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (41619442..41624575, complement) | 39.1, CK-17, K17, PC, PC2, PCHC1 | 148069 |
ID: 11202 | kallikrein related peptidase 8 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50996008..51001604, complement) | HNP, NP, NRPN, PRSS19, TADG14 | 605644 |
ID: 7020 | transcription factor AP-2 alpha [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (10396677..10419659, complement) | AP-2, AP-2alpha, AP2TF, BOFS, TFAP2 | 107580 |
ID: 25818 | kallikrein related peptidase 5 [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (50943303..50953038, complement) | KLK-L2, KLKL2, SCTE | 605643 |