Source: CLINVAR

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 25906
Gene Symbol: ANAPC15
ANAPC15
anaphase promoting complex subunit 15 1.000 0.115 0.30
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 1
Entrez Id: 286262
Gene Symbol: TPRN
TPRN
taperin 0.839 0.115 7.2E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 strong 1.000 0 2 2010 2010
Entrez Id: 389207
Gene Symbol: GRXCR1
GRXCR1
glutaredoxin and cysteine rich domain containing 1 0.861 0.115 3.9E-11
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.410 strong 1.000 0 1 2010 2010
Entrez Id: 494513
Gene Symbol: PJVK
PJVK
pejvakin 0.769 0.115 3.7E-08
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.420 strong 1.000 0 1 2007 2007
Entrez Id: 113444
Gene Symbol: SMIM12
SMIM12
small integral membrane protein 12 0.780 0.192 0.57
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 1
Entrez Id: 161497
Gene Symbol: STRC
STRC
stereocilin 0.700 0.192 1.8E-15
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.150 None 1.000 0 1 2012 2019
Entrez Id: 220074
Gene Symbol: LRTOMT
LRTOMT
leucine rich transmembrane and O-methyltransferase domain containing 0.792 0.192 7.0E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.430 strong 1.000 0 1 2007 2012
Entrez Id: 222662
Gene Symbol: LHFPL5
LHFPL5
LHFPL tetraspan subfamily member 5 0.861 0.192 4.0E-04
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.120 None 1.000 0 1 2018 2019
Entrez Id: 126326
Gene Symbol: GIPC3
GIPC3
GIPC PDZ domain containing family member 3 0.780 0.231 9.3E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 strong 1.000 0 1 1997 1997
Entrez Id: 414152
Gene Symbol: C10orf105
C10orf105
chromosome 10 open reading frame 105 0.861 0.231 8.4E-02
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 1
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP
TRIO and F-actin binding protein 0.743 0.269 2.0E-28
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.430 strong 1.000 0 6 2006 2017
Entrez Id: 283310
Gene Symbol: OTOGL
OTOGL
otogelin like 0.805 0.269 4.7E-52
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.120 None 1.000 0 1 2013 2019
Entrez Id: 286002
Gene Symbol: SLC26A4-AS1
SLC26A4-AS1
SLC26A4 antisense RNA 1 0.861 0.269
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 5
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A
myosin IIIA 0.780 0.269 1.8E-45
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.410 strong 1.000 0 4 2011 2016
Entrez Id: 253827
Gene Symbol: MSRB3
MSRB3
methionine sulfoxide reductase B3 0.729 0.308 3.8E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.600 strong 1.000 0 1 2011 2014
Entrez Id: 5435
Gene Symbol: POLR2F
POLR2F
RNA polymerase II subunit F 0.722 0.308 1.3E-02
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 1
Entrez Id: 1159
Gene Symbol: CKMT1B
CKMT1B
creatine kinase, mitochondrial 1B 0.729 0.346 3.2E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 1
Entrez Id: 117531
Gene Symbol: TMC1
TMC1
transmembrane channel like 1 0.769 0.346 9.2E-19
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.450 strong 0.833 0 4 2004 2015
Entrez Id: 124590
Gene Symbol: USH1G
USH1G
USH1 protein network component sans 0.659 0.346 3.7E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.620 strong 1.000 0 3 2014 2019
Entrez Id: 286676
Gene Symbol: ILDR1
ILDR1
immunoglobulin like domain containing receptor 1 0.729 0.346 2.6E-12
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.420 strong 1.000 0 3 2011 2019
Entrez Id: 388939
Gene Symbol: PCARE
PCARE
photoreceptor cilium actin regulator 0.674 0.346 3.0E-18
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.100 None 0 1
Entrez Id: 51168
Gene Symbol: MYO15A
MYO15A
myosin XVA 0.722 0.346 1.3E-56
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.430 strong 1.000 0 15 1998 2019
Entrez Id: 25861
Gene Symbol: WHRN
WHRN
whirlin 0.670 0.385 7.7E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.430 strong 1.000 0 1 2009 2019
Entrez Id: 7007
Gene Symbol: TECTA
TECTA
tectorin alpha 0.700 0.385 3.0E-16
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.500 strong 1.000 0 4 1998 2018
Entrez Id: 83715
Gene Symbol: ESPN
ESPN
espin 0.700 0.385 2.9E-09
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.120 None 1.000 0 1 2006 2008