Premature Ovarian Failure 5; Pof5

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Premature Ovarian Failure 5; Pof5

NOBOX

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Premature Ovarian Failure 5; Pof5

Primary amenorrhea
Premature ovarian insufficiency
Secondary amenorrhea

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Premature Ovarian Failure 5; Pof5 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Premature Ovarian Failure Sequencing Panel. By Genetic Services Laboratory University of Chicago (United States). BMP15, FOXL2, MCM8, PSMC3IP, HFM1, NOBOX, FIGLA, FSHR, LMNA, NR5A1 Specificity 10 % Genes 100 %
Premature Ovarian Failure Deletion/Duplication Panel. By Genetic Services Laboratory University of Chicago (United States). BMP15, FOXL2, MCM8, PSMC3IP, HFM1, NOBOX, FIGLA, FSHR, LMNA, NR5A1 Specificity 10 % Genes 100 %
Female Infertility Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). BMP15, SEMA3A, SEMA3E, FOXL2, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, TAC3, TACR3, WNT4, WT1, WWOX, ZP1, ARL6 , (...) View the complete list with 84 more genes Panel complete gene list BMP15, SEMA3A, SEMA3E, FOXL2, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, TAC3, TACR3, WNT4, WT1, WWOX, ZP1, ARL6, WDR11, CBX2, SPRY4, PROKR2, MCM8, TRIM32, IL17RD, PSMC3IP, ARX, PROK2, BBS7, TTC8, HFM1, PADI6, CHD7, CLPP, MCM9, RSPO1, LHX4, NOBOX, FEZF1, FIGLA, MAMLD1, CYP11A1, CYP17A1, CYP19A1, BBS10, BBS12, CCDC141, SOHLH1, DHH, SYCE1, DMRT1, DMRT2, NSMF, NUP107, BBS9, DUSP6, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, AIRE, FGF17, FGF8, FGFR1, FGFR2, FLRT3, AKR1C4, FSHB, FSHR, GALT, GNRH1, GNRHR, KISS1R, HESX1, HFE, HS6ST1, HSD17B3, ANOS1, KISS1, AR, LEP, LEPR, LHB, LHCGR, LHX3, LMNA, MAP3K1, MKKS, NR0B1, NR3C1, NR5A1, PCSK1, ATRX, AXL, POR, PRLR, PROP1, BBS1, BBS2, BBS4, BBS5 Specificity 1 % Genes 100 %
Disorders of Sex Development (DSD) and Infertility Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). ROR2, SALL1, BMP15, BMP4, SEMA3A, SEMA3E, BMP7, FOXL2, BRDT, SOS1, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, AURKC , (...) View the complete list with 187 more genes Panel complete gene list ROR2, SALL1, BMP15, BMP4, SEMA3A, SEMA3E, BMP7, FOXL2, BRDT, SOS1, SOX10, SOX2, SOX3, SOX9, SRA1, SRD5A2, SRY, STAG3, STAR, AURKC, TAC3, TACR3, TAF4B, TBX15, HNF1B, TEX11, MED12, CEP41, TSPYL1, WNT4, WNT5A, WNT7A, WT1, WWOX, ZP1, ARL6, FBXL4, WDR11, SLC26A8, ZEB2, CBX2, SPRY4, SETBP1, PROKR2, TOE1, TP63, PCNT, MCM8, SUN5, TRIM32, ZFPM2, UBR1, FIG4, CATSPER1, IL17RD, CDKN1C, PSMC3IP, ARX, SYCP3, HHAT, PROK2, GRIP1, BBS7, KLHL10, CFTR, FRAS1, CHD4, PLCZ1, EVC2, TTC8, HFM1, B3GLCT, PADI6, CHD7, TWIST2, CLPP, BCOR, ZMYND15, CUL7, ICK, MCM9, RSPO1, GALNTL5, LHX4, WDR60, NOBOX, FEZF1, NANOS1, FAT4, CREBBP, FIGLA, FREM2, CFAP44, MAMLD1, CYB5A, CYP11A1, CYP11B1, CYP17A1, CYP19A1, TMEM70, BBS10, SEPT12, BBS12, CFAP43, CCDC141, ESCO2, SOHLH1, CCNQ, DHCR24, DHCR7, DHH, SYCE1, SPECC1L, WDR35, EPG5, DMRT1, DMRT2, DNAH1, DYNC2H1, DNMT3B, NSMF, NUP107, SPATA16, BBS9, DUSP6, TRAIP, BNC2, EFNB1, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, EVC, AIRE, FGF10, FGF17, FGF8, FGFR1, FGFR2, FGFR3, FLNA, FLRT3, AKR1C4, FSHB, FSHR, GALT, GATA4, GLI3, GNRH1, GNRHR, GPC3, KISS1R, ADGRG2, AMH, AMHR2, HBA1, HCCS, HESX1, HFE, RIPK4, HOXA13, HOXA4, HOXB6, HS6ST1, HSD17B3, HSD17B4, HSD3B2, INSL3, IRF6, ANOS1, KISS1, AR, LEP, LEPR, LHB, LHCGR, LHX3, LMNA, MAP3K1, MID1, MKKS, MKS1, NEK1, ATF3, NPAS2, NR0B1, NR3C1, NR5A1, OPHN1, PCSK1, PDE4D, PEX1, ATRX, PITX2, AXL, POR, PICK1, PRLR, PROP1, PTDSS1, PTPN11, BBS1, BBS2, BBS4, BBS5, RBBP8 Specificity 1 % Genes 100 %
Premature Ovarian Failure (POF) Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). BMP15, FOXL2, STAG3, MCM8, PSMC3IP, HFM1, CLPP, MCM9, NOBOX, FIGLA, CYP17A1, CYP19A1, SOHLH1, EIF2B2, EIF2B4, EIF2B5, AIRE, FSHR, GALT, LMNA , (...) View the complete list with 1 more genes Panel complete gene list BMP15, FOXL2, STAG3, MCM8, PSMC3IP, HFM1, CLPP, MCM9, NOBOX, FIGLA, CYP17A1, CYP19A1, SOHLH1, EIF2B2, EIF2B4, EIF2B5, AIRE, FSHR, GALT, LMNA, NR5A1 Specificity 5 % Genes 100 %
Endocrine Disorders: Sequencing Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics (United States). BLK, BMP15, SLC2A2, TAC3, TACR3, HNF1A, HNF1B, KLF11, WFS1, ZMPSTE24, BSCL2, PROKR2, PSMC3IP, PROK2, IER3IP1, TBC1D4, CHD7, RFX6, NOBOX, PTF1A , (...) View the complete list with 37 more genes Panel complete gene list BLK, BMP15, SLC2A2, TAC3, TACR3, HNF1A, HNF1B, KLF11, WFS1, ZMPSTE24, BSCL2, PROKR2, PSMC3IP, PROK2, IER3IP1, TBC1D4, CHD7, RFX6, NOBOX, PTF1A, CISD2, CIDEC, FIGLA, CYP17A1, CYP19A1, GLIS3, NSMF, AGPAT2, EIF2AK3, FGF8, FGFR1, AKT2, FSHR, GATA6, GCK, GDF9, GNRH1, GNRHR, KISS1R, HADH, HNF4A, ABCC8, INS, INSR, FOXP3, PDX1, KCNJ11, KISS1, LHCGR, LMNA, NEUROD1, NR0B1, NR5A1, PAX4, POR, PPARG, CAVIN1 Specificity 2 % Genes 100 %
Endocrine Disorders: Deletion/Duplication Panel. By EGL Genetic Diagnostics Eurofins Clinical Diagnostics (United States). BLK, BMP15, SLC2A2, TAC3, TACR3, HNF1A, HNF1B, KLF11, WFS1, ZMPSTE24, BSCL2, PROKR2, PSMC3IP, PROK2, IER3IP1, TBC1D4, CHD7, RFX6, NOBOX, PTF1A , (...) View the complete list with 37 more genes Panel complete gene list BLK, BMP15, SLC2A2, TAC3, TACR3, HNF1A, HNF1B, KLF11, WFS1, ZMPSTE24, BSCL2, PROKR2, PSMC3IP, PROK2, IER3IP1, TBC1D4, CHD7, RFX6, NOBOX, PTF1A, CISD2, CIDEC, FIGLA, CYP17A1, CYP19A1, GLIS3, NSMF, AGPAT2, EIF2AK3, FGF8, FGFR1, AKT2, FSHR, GATA6, GCK, GDF9, GNRH1, GNRHR, KISS1R, HADH, HNF4A, ABCC8, INS, INSR, FOXP3, PDX1, KCNJ11, KISS1, LHCGR, LMNA, NEUROD1, NR0B1, NR5A1, PAX4, POR, PPARG, CAVIN1 Specificity 2 % Genes 100 %
NOBOX. By Fulgent Genetics Fulgent Genetics (United States). NOBOX Specificity 100 % Genes 100 %

You can get up to 4 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SMITH-MAGENIS SYNDROME MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL; CMS1A EPILEPSY, IDIOPATHIC GENERALIZED; EIG HYPERMANGANESEMIA WITH DYSTONIA 1; HMNDYT1 CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2H; CMT2H RUIJS-AALFS SYNDROME; RJALS POLYCYTHEMIA VERA; PV