Endocrinology disorder panel (226 genes)
The genetic variants in 226 genes analyzed in this panel are closely related to or, potentially, the cause of major endocrinological conditions.
Genes included in the Endocrinology Disorder Panel include:
ABCA1, ABCC8, ABCG5, ABCG8, ACAT1, ACSF3, ADCY3, AGL, AIRE, ALDOA, ALDOB, ALMS1, AMH, AMHR2, ANOS1, AP2S1, APOA1, APOA5, APOB, APOC2, APOC3, APOE, AR, ARL6, ARMC5, ARX, ATRX, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BLK, BMP15, BSND, CASR, CDC73, CDKN1A, CDKN1B, CDKN1C, CDKN2B, CDKN2C, CEP290, CEP41, CHD7, CLCNKB, CLDN16, CLDN19, CNNM2, CNNM4, CREB3L3, CREBBP, CUL4B, CYP11A1, CYP11B1, CYP17A1, CYP19A1, CYP21A2, DHCR7, DHH, DUOX2, DUOXA2, DYNC2H1, DYRK1B, EGF, EIF2AK3, ENO3, EPM2A, ERCC3, FAM111A, FBP1, FGF8, FGFR1, FIG4, FOXE1, FOXL2, FOXP3, FRAS1, FSHR, FXYD2, GAA, GALT, GATA4, GATA6, GBE1, GCK, GCM2, GLIS3, GLUD1, GNA11, GNAS, GNRHR, GPIHBP1, GYG1, GYS1, GYS2, HADH, HESX1, HMGCL, HMGCS2, HNF1A, HNF1B, HNF4A, HSD17B3, HSD3B2, IGSF1, IL17RD, INS, INSR, IRF6, KCNA1, KCNJ10, KCNJ11, KISS1R, KLF11, KSR2, LAMP2, LDHA, LDLR, LDLRAP1, LEP, LEPR, LHCGR, LIPA, LMF1, LMNA, LPL, MAGEL2, MAGT1, MAMLD1, MAP3K1, MC2R, MC3R, MC4R, MEN1, MKKS, MKRN3, MKS1, MPV17, MRAP, NEUROD1, NEUROG3, NHLRC1, NIPA2, NKX2-1, NKX2-5, NNT, NOBOX, NR0B1, NR0B2, NR3C1, NR5A1, NTRK2, OXCT1, PAX4, PAX8, PC, PCBD1, PCK1, PCSK1, PCSK9, PDX1, PFKM, PGAM2, PGK1, PGM1, PHF6, PHKA1, PHKA2, PHKB, PHKG2, POLG, POMC, POR, POU1F1, PPARG, PRKAG2, PRKAG3, PRKAR1A, PROK2, PROKR2, PROP1, PTF1A, PTH, PYGL, PYGM, RBCK1, RET, RFX6, RSPO1, SARS2, SDCCAG8, SECISBP2, SIM1, SLC12A3, SLC16A1, SLC16A2, SLC26A4, SLC2A2, SLC37A4, SLC5A5, SOX9, SRD5A2, SRY, STAR, TACR3, TG, THRA, THRB, TPO, TRPM6, TSHB, TSHR, TTC8, UCP2, UCP3, VPS13B, WDPCP, WFS1, WT1, ZFP57, ZFPM2.
