Deafness, Autosomal Recessive 107; Dfnb107

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 Deafness, Autosomal Recessive 107; Dfnb107

WBP2

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Deafness, Autosomal Recessive 107; Dfnb107

Hearing impairment

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.

Deafness, Autosomal Recessive 107; Dfnb107 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
WBP2. By Fulgent Genetics Fulgent Genetics (United States). WBP2 Specificity 100 % Genes 100 %
Comprehensive Hearing Loss and Deafness Panel. By Blueprint Genetics (Finland). BCS1L, RPS6KA3, SALL1, SEMA3E, SIX1, SIX5, SLC19A2, SNAI2, SMPX, SOX10, BTD, SUCLA2, SUCLG1, TWNK, TCOF1, TECTA, TFAP2A, TIMM8A, TJP2, TMPRSS3 , (...) View the complete list with 157 more genes Panel complete gene list BCS1L, RPS6KA3, SALL1, SEMA3E, SIX1, SIX5, SLC19A2, SNAI2, SMPX, SOX10, BTD, SUCLA2, SUCLG1, TWNK, TCOF1, TECTA, TFAP2A, TIMM8A, TJP2, TMPRSS3, TYR, USH1C, USH2A, CLRN1, TSPEAR, WBP2, WFS1, ESPN, CLIC5, BDP1, CDH23, CABP2, RIPOR2, CACNA1D, ACTG1, PCDH15, P2RX2, DIAPH3, ANKH, OSBPL2, ABHD12, SALL4, STRC, SLC52A3, CD151, CD164, USH1G, WHRN, OTOA, NLRP3, BSND, TMC1, TRIOBP, LARS2, CDC14A, CHSY1, ADGRV1, HOMER2, CDKN1C, CCDC50, SPATA5, DCDC2, GIPC3, SLC17A8, POLR1C, CLDN14, POLR1D, CHD7, CLPP, RMND1, LHFPL5, EPS8L2, DIABLO, COCH, COL11A1, COL11A2, COL4A3, COL4A4, COL4A5, COL4A6, COL9A1, COL9A2, COL9A3, PEX26, SLC29A3, PNPT1, ADCY1, MYH14, SLITRK6, CRYM, CIB2, LRTOMT, TRMU, CEP78, DCAF17, ELMOD3, PDZD7, NARS2, MARVELD2, LOXHD1, SYNE4, TPRN, OTOGL, TMEM132E, MSRB3, GRHL2, GSDME, ILDR1, DIAPH1, DLX5, TBC1D24, GPSM2, PJVK, DNMT1, SLC52A2, DSPP, TMIE, MIR96, GRXCR1, S1PR2, EDN3, EDNRB, CEACAM16, GRXCR2, EPS8, ESRRB, EYA1, EYA4, FDXR, FGF3, FGFR3, FOXI1, GATA3, GJA1, ALMS1, GJB2, GJB6, HARS, HARS2, HGF, HOXB1, HSD17B4, TNC, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, LRP2, SMAD4, MAN2B1, MANBA, MET, MGP, MITF, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NDP, OTOF, OTOG, ATP6V1B1, ATP6V1B2, PAX3, AIFM1, SLC26A4, PEX1, PEX6, SERPINB6, POU3F4, POU4F3, SLC26A5, PRPS1, SLC33A1, RDX Specificity 1 % Genes 100 %
Non-Syndromic Hearing Loss Panel. By Blueprint Genetics (Finland). SIX1, SMPX, TECTA, TJP2, TMPRSS3, USH1C, TSPEAR, WBP2, WFS1, ESPN, CLIC5, BDP1, CDH23, CABP2, RIPOR2, ACTG1, PCDH15, P2RX2, DIAPH3, OSBPL2 , (...) View the complete list with 74 more genes Panel complete gene list SIX1, SMPX, TECTA, TJP2, TMPRSS3, USH1C, TSPEAR, WBP2, WFS1, ESPN, CLIC5, BDP1, CDH23, CABP2, RIPOR2, ACTG1, PCDH15, P2RX2, DIAPH3, OSBPL2, STRC, CD164, WHRN, OTOA, BSND, TMC1, TRIOBP, CDC14A, HOMER2, CCDC50, DCDC2, GIPC3, SLC17A8, CLDN14, LHFPL5, EPS8L2, DIABLO, COCH, COL11A2, COL4A6, PNPT1, ADCY1, MYH14, SLITRK6, CRYM, CIB2, LRTOMT, ELMOD3, NARS2, MARVELD2, LOXHD1, SYNE4, TPRN, OTOGL, TMEM132E, MSRB3, GRHL2, GSDME, ILDR1, DIAPH1, TBC1D24, GPSM2, PJVK, DSPP, TMIE, MIR96, GRXCR1, S1PR2, CEACAM16, GRXCR2, EPS8, ESRRB, EYA4, GJB2, GJB6, HGF, TNC, KARS, KCNQ4, MET, MYH9, MYO15A, MYO3A, MYO6, MYO7A, OTOF, OTOG, SLC26A4, SERPINB6, POU3F4, POU4F3, SLC26A5, PRPS1, RDX Specificity 2 % Genes 100 %
DEAFNESS, NONSYNDROMIC SENSORINEURAL (AUTOSOMAL RECESSIVE) NGS PANEL. By Laboratorio de Genetica Clinica SL (Spain). SLC12A1, SMPX, TECTA, TMPRSS3, USH1C, TSPEAR, WBP2, CLIC5, CDH23, CABP2, RIPOR2, PCDH15, STRC, WHRN, BSND, TMC1, TRIOBP, CDC14A, DCDC2, GIPC3 , (...) View the complete list with 42 more genes Panel complete gene list SLC12A1, SMPX, TECTA, TMPRSS3, USH1C, TSPEAR, WBP2, CLIC5, CDH23, CABP2, RIPOR2, PCDH15, STRC, WHRN, BSND, TMC1, TRIOBP, CDC14A, DCDC2, GIPC3, CLDN14, LHFPL5, COL11A2, COL4A6, PNPT1, ADCY1, CIB2, LRTOMT, ELMOD3, MARVELD2, LOXHD1, SYNE4, TPRN, OTOGL, MSRB3, ILDR1, GPSM2, PJVK, TMIE, GRXCR1, S1PR2, GRXCR2, EPS8, ESRRB, FOXI1, GJB2, GJB6, HGF, KCNJ10, MYO15A, MYO3A, MYO6, MYO7A, OTOF, OTOG, SLC26A4, SERPINB6, POU3F4, SLC26A5, PRPS1, PTPRQ, RDX Specificity 2 % 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 Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like SESSILE SERRATED POLYPOSIS CANCER SYNDROME; SSPCS WERNER SYNDROME; WRN ISOLATED BRACHYCEPHALY GLYCOGEN STORAGE DISEASE Ib; GSD1B CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE ANEMIA, X-LINKED, WITH OR WITHOUT NEUTROPENIA AND/OR PLATELET ABNORMALITIES; XLANP RETINITIS PIGMENTOSA 78; RP78