Test Code: PNL231

Genes: ACE, ACTG2, ACTN4, AGT, AGTR1, AGXT, AHI1, ALG5, ALG8, ALG9, ALMS1, AMN, ANKS6, ANOS1, AP2S1, APOA1, APOA2, APOC2, APOE, APRT, AQP2, ARHGDIA, ARL13B, ARL6, ARMC9, ATP1A1, ATP6V0A4, ATP6V1B1, AVPR2, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BNC2, BSND, C3, CA2, CASR, CC2D2A, CD151, CD46, CENPF, CEP104, CEP164, CEP290, CEP41, CEP83, CFB, CFH, CFHR1, CFHR2, CFHR3, CFHR5, CFI, CHD7, CHRM3, CILK1, CLCN5, CLCNKB, CLDN10, CLDN16, CLDN19, CNNM2, COL4A1, COL4A3, COL4A4, COL4A5, COQ2, COQ6, COQ8B, CPLANE1, CRB2, CSPP1, CTNS, CUBN, CUL3, CYP24A1, DAAM2, DDX59, DGKE, DHCR7, DLC1, DLG5, DNAJB11, DSTYK, DYNC2H1, DYNC2I1, DZIP1L, EYA1, FAH, FAM20A, FAN1, FAT1, FGA, FLCN, FN1, FRAS1, FREM1, FREM2, GANAB, GATA3, GATM, GLA, GLI3, GLIS2, GNA11, GON7, GRHPR, GRIP1, GSN, HAAO, HNF1B, HNF4A, HOGA1, HPRT1, HPSE2, HYLS1, IFT122, IFT140, IFT172, IFT27, IFT43, INF2, INPP5E, INVS, IQCB1, ITGA3, ITGA8, ITSN1, KCNJ1, KCNJ10, KCNJ16, KIAA0586, KIAA0753, KIF7, KLHL3, KYNU, LAGE3, LAMB2, LCAT, LMX1B, LRIG2, LYZ, LZTFL1, MAGED2, MAGI2, MAPKBP1, MKKS, MKS1, MMACHC, MOCOS, MT-TF, MUC1, MYH9, MYO1E, NEK8, NOS1AP, NPHP1, NPHP3, NPHP4, NPHS1, NPHS2, NR3C2, NUP107, NUP133, NUP85, NUP93, OCRL, OFD1, OSGEP, PAX2, PBX1, PDSS2, PHEX, PKD1, PKD2, PKHD1, PLCE1, PMM2, PODXL, PRDM15, PRKCSH, PSKH1, REN, RET, RMND1, RPGRIP1L, RRAGD, RRM2B, SALL1, SARS2, SCARB2, SCNN1A, SCNN1B, SCNN1G, SDCCAG8, SEC61A1, SEC63, SGPL1, SIX5, SLC12A1, SLC12A3, SLC22A12, SLC2A2, SLC2A9, SLC34A1, SLC34A3, SLC3A1, SLC4A1, SLC4A4, SLC5A2, SLC7A9, SMARCAL1, STRADA, TBC1D8B, TBX18, TCTN1, TCTN2, TCTN3, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM67, TNS2, TP53RK, TPRKB, TRAF3IP1, TRAP1, TRIM8, TRPC6, TRPM6, TSC1, TSC2, TTC21B, TTC8, TTR, TULP3, TXNDC15, UMOD, VHL, VIPAS39, VPS33B, WDPCP, WDR19, WDR35, WDR72, WDR73, WNK4, WT1, XDH, XPNPEP3, YRDC (259 genes)

Sample Type: 3 ml peripheral blood in EDTA (purple/pink top) tube

Method: Capture-based target enrichment and Next Generation Sequencing.

Turnaround Time: 3 weeks

Courier: Ship overnight at room temperature to receive next day. Do not refrigerate or freeze. Maintain specimen at room temperature.

Price: 1800

Description:
The Renal Failure Gene Panel - Unexplained, is a broad genetic test that screens for mutations across ~259 genes implicated in diverse kidney disorders. It is particularly valuable for patients with early-onset or unexplained renal failure, offering diagnostic clarity, prognostic insight, and guidance for family counseling.