ID: 169026 | solute carrier family 30 member 8 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (116950217..117176714) | ZNT8, ZnT-8 | 611145 |
ID: 56729 | resistin [Homo sapiens (human)] | Chromosome 19, NC_000019.10 (7669049..7670455) | ADSF, FIZZ3, RENT1, RSTN, XCP1, RETN | 605565 |
ID: 10644 | insulin like growth factor 2 mRNA binding protein 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (185643130..185825042, complement) | IMP-2, IMP2, VICKZ2 | 608289 |
ID: 9479 | mitogen-activated protein kinase 8 interacting protein 1 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (45885651..45906465) | IB1, JIP-1, JIP1, PRKM8IP | 604641 |
ID: 8660 | insulin receptor substrate 2 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (109752695..109786583, complement) | IRS-2 | 600797 |
ID: 7466 | wolframin ER transmembrane glycoprotein [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (6269850..6303265) | CTRCT41, WFRS, WFS, WFSL | 606201 |
ID: 6934 | transcription factor 7 like 2 [Homo sapiens (human)] | Chromosome 10, NC_000010.11 (112950247..113167678) | TCF-4, TCF4 | 602228 |
ID: 6928 | HNF1 homeobox B [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (37686431..37745059, complement) | ADTKD3, FJHN, HNF-1-beta, HNF-1B, HNF1beta, HNF2, HPC11, LF-B3, LFB3, MODY5, RCAD, T2D, TCF-2, TCF2, VHNF1 | 189907 |
ID: 6927 | HNF1 homeobox A [Homo sapiens (human)] | Chromosome 12, NC_000012.12 (120978543..121002512) | HNF-1-alpha, HNF-1A, HNF1, HNF1alpha, HNF4A, IDDM20, LFB1, MODY3, TCF-1, TCF1 | 142410 |
ID: 6833 | ATP binding cassette subfamily C member 8 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17392498..17476845, complement) | ABC36, HHF1, HI, HRINS, MRP8, PHHI, PNDM3, SUR, SUR1, SUR1delta2, TNDM2 | 600509 |
ID: 6514 | solute carrier family 2 member 2 [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (170996347..171026720, complement) | GLUT2 | 138160 |
ID: 5770 | protein tyrosine phosphatase non-receptor type 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50510383..50585241) | PTP1B | 176885 |
ID: 5506 | protein phosphatase 1 regulatory subunit 3A [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (113876777..113919009, complement) | GM, PP1G, PPP1R3 | 600917 |
ID: 5468 | peroxisome proliferator activated receptor gamma [Homo sapiens (human)] | Chromosome 3, NC_000003.12 (12287368..12434344) | CIMT1, GLM1, NR1C31, PPARG2, PPARG5, PPARgamma, PPARG | 601487 |
ID: 5167 | ectonucleotide pyrophosphatase/phosphodiesterase 1 [Homo sapiens (human)] | Chromosome 6, NC_000006.12 (131808020..131895155) | ARHR2, COLED, M6S1, NPP1, NPPS, PC-1, PCA1, PDNP1 | 173335 |
ID: 5078 | paired box 4 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (127610292..127618142, complement) | KPD, MODY9 | 167413 |
ID: 4760 | neuronal differentiation 1 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (181668295..181680517, complement) | BETA2, BHF-1, MODY6, NEUROD, T2D, bHLHa3 | 601724 |
ID: 4544 | melatonin receptor 1B [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (92969651..92984960) | FGQTL2, MEL-1B-R, MT2 | 600804 |
ID: 3990 | lipase C, hepatic type [Homo sapiens (human)] | Chromosome 15, NC_000015.10 (58431991..58569844) | HDLCQ12, HL, HTGL, LIPH | 151670 |
ID: 3767 | potassium inwardly rectifying channel subfamily J member 11 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (17385248..17389346, complement) | BIR, HHF2, IKATP, KIR6.2, MODY13, PHHI, PNDM2, TNDM3 | 600937 |