Table 1a: Female gene panel information.
Detection item |
Detection gene |
Premature ovarian failure related genes (35) |
PSMC3IP, FSHR, NOBOX, BMP15, FIGLA, FMR1, ERCC6, FOXL2, HFM1, MCM8, POF1B, STAG3, NR5A1, SYCE1, EIF2B2, EIF2B4, EIF2B5, MSH5, MCM9, SOHLH1, CLPP, ERAL1, HSD17B4, AMH, SOX9, DIAPH2, LMNA, FANCM, POF1B, GDF9, AARS2, ESR2, MRPS22, NUP107, BRCA2 |
Genes related to oocyte maturation defects, fertilization and embryo development abnormalities (11) |
TUBB8, ZP1, PATL2, ZP3, ZP2, PADI6, WEE2, TLE6, ZP4, KHDC3L, PANX1 |
Genes related to idiopathic hypogonadotropic hypogonadism (33) |
TACR3, TAC3, WDR11, KISS1, KISS1R, SPRY4, IL17RD, FEZF1, FGF17, FLRT3, GNRH1, GNRHR, DUSP6, LHB, FGFR1, PROKR2, FGF8, PROK2, CHD7, ANOS1, LHCGR, POR, HS6ST1, SEMA3A, NSMF, NR0B1, PNPLA6, SMCHD1, POLR3B, POLR3A, RNF216, SOX2, SOX10 |