Source: GENOMICS_ENGLAND

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: 87178
Gene Symbol: PNPT1
PNPT1
polyribonucleotide nucleotidyltransferase 1 0.653 0.462 4.0E-04
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 None 1.000 2 0 2012 2016
Entrez Id: 4330
Gene Symbol: MN1
MN1
MN1 proto-oncogene, transcriptional regulator 0.682 0.385 1.00
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 None 1.000 1 0 2005 2005
Entrez Id: 51399
Gene Symbol: TRAPPC4
TRAPPC4
trafficking protein particle complex 4 0.805 0.308 4.1E-06
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 None 1.000 1 0 2020 2020
Entrez Id: 686
Gene Symbol: BTD
BTD
biotinidase 0.628 0.654 1.5E-07
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 None 0 0
Entrez Id: 5308
Gene Symbol: PITX2
PITX2
paired like homeodomain 2 0.489 0.808 0.98
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 None 0 0
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
fibroblast growth factor receptor 3 0.391 0.846 1.6E-05
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.410 None 1.000 0 0 2015 2015
Entrez Id: 411
Gene Symbol: ARSB
ARSB
arylsulfatase B 0.595 0.692 7.0E-09
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 None 0 0
Entrez Id: 51099
Gene Symbol: ABHD5
ABHD5
abhydrolase domain containing 5 0.641 0.538 6.4E-07
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 None 0 0
Entrez Id: 493856
Gene Symbol: CISD2
CISD2
CDGSH iron sulfur domain 2 0.590 0.692 0.42
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 None 0 0
Entrez Id: 6197
Gene Symbol: RPS6KA3
RPS6KA3
ribosomal protein S6 kinase A3 0.491 0.846 1.00
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 None 0 0
Entrez Id: 2189
Gene Symbol: FANCG
FANCG
FA complementation group G 0.556 0.769 2.5E-14
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 strong 1.000 2 0 1998 2006
Entrez Id: 2176
Gene Symbol: FANCC
FANCC
FA complementation group C 0.507 0.808 2.8E-13
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 strong 1.000 2 0 1992 2006
Entrez Id: 2175
Gene Symbol: FANCA
FANCA
FA complementation group A 0.505 0.731 1.6E-68
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.400 strong 1.000 2 0 1996 2006
Entrez Id: 64699
Gene Symbol: TMPRSS3
TMPRSS3
transmembrane serine protease 3 0.650 0.538 6.1E-11
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.460 strong 1.000 1 0 2003 2014
Entrez Id: 7399
Gene Symbol: USH2A
USH2A
usherin 0.579 0.692 1.6E-94
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.480 strong 1.000 1 0 1998 2019
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 1 0 1998 2019
Entrez Id: 7401
Gene Symbol: CLRN1
CLRN1
clarin 1 0.633 0.423 1.7E-08
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.330 strong 1.000 1 0 1998 2019
Entrez Id: 7809
Gene Symbol: BSND
BSND
barttin CLCNK type accessory subunit beta 0.603 0.692 1.1E-10
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 strong 1.000 1 0 1998 1998
Entrez Id: 79977
Gene Symbol: GRHL2
GRHL2
grainyhead like transcription factor 2 0.590 0.731 1.00
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.330 strong 0.750 1 0 2008 2019
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
myosin VIIA 0.585 0.423 1.6E-38
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.500 strong 1.000 1 0 1998 2019
Entrez Id: 84059
Gene Symbol: ADGRV1
ADGRV1
adhesion G protein-coupled receptor V1 0.572 0.731 3.2E-39
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.410 strong 1.000 1 0 1998 2019
Entrez Id: 7466
Gene Symbol: WFS1
WFS1
wolframin ER transmembrane glycoprotein 0.528 0.846 1.6E-38
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.500 strong 1.000 1 0 1998 2017
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 1 0 2010 2010
Entrez Id: 375611
Gene Symbol: SLC26A5
SLC26A5
solute carrier family 26 member 5 0.666 0.615 7.0E-08
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.320 strong 1.000 1 0 2005 2016
Entrez Id: 3295
Gene Symbol: HSD17B4
HSD17B4
hydroxysteroid 17-beta dehydrogenase 4 0.546 0.654 2.4E-10
CUI: C1384666
Disease: hearing impairment
hearing impairment
phenotype 0.300 strong 1.000 1 0 1999 1999