SNPMiner Trials by Shray Alag

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SNPMiner SNPMiner Trials (Home Page)


Report for Mutation R135W

Developed by Shray Alag, 2020.
SNP Clinical Trial Gene

There is one clinical trial.

Clinical Trials


1 A Prospective, Multicenter, Longitudinal, Observational Natural History Study to Evaluate Disease Progression in Subjects With Autosomal Dominant Retinitis Pigmentosa (adRP) With Misfolded Rod Opsin Mutations

The purpose of this study is to gain an understanding of how adRP progresses over time in patients with misfolded rod opsin mutations.

NCT02926092
Conditions
  1. Retinitis Pigmentosa
Interventions
  1. Diagnostic Test: Observation
MeSH:Retinitis Retinitis Pigmentosa
HPO:Cone/cone-rod dystrophy Pigmentary retinopathy Rod-cone dystrophy

The subject has 1 documented pre-specified heterozygous rhodopsin gene (RHO) mutation confirmed by genetic testing (mutations will include P23H, T17M, and R135W). --- P23H --- --- T17M --- --- R135W ---

Primary Outcomes

Measure: Progression of disease over time in adRP patients with misfolded rod opsin mutations using ellipsoid zone (EZ) area measurements

Time: Baseline to 4 years

Secondary Outcomes

Measure: Progression of disease over time in adRP patients with misfolded rod opsin mutations as measured by EZ width

Time: Baseline to 4 years

Measure: Progression of disease over time in adRP patients with misfolded rod opsin mutations as measured by visual fields (kinetic and static)

Time: Baseline to 4 years

Measure: Progression of disease over time in adRP patients with misfolded rod opsin mutations as measured by dark-adapted rod visual fields

Time: Baseline to 4 years

Measure: Progression of disease over time in adRP patients with misfolded rod opsin mutations as measured by electroretinography (ERG): dark- and light-adapted

Time: Baseline to 4 years

Measure: Progression of disease over time in adRP patients with misfolded rod opsin mutations as measured by best corrected visual acuity (BCVA)

Time: Baseline to 4 years

Measure: Vision-related function and quality of life as measured by 25-item National Eye Institute Visual Function Questionnaire (NEI VFQ-25) plus its additional items

Time: Baseline to 4 years


HPO Nodes


HP:0000510: Rod-cone dystrophy
Genes 259
GAS8 PEX1 DNAL1 SNRNP200 CWC27 APOB ND4 ABCA4 POGZ CCDC40 RBP3 RSPH4A PEX5 PEX11B CEP290 NR2E3 DNAH9 FAM161A PHYH LRAT PEX7 PRPH2 ARL3 BBS10 NEK2 PDZD7 BBS7 CNGA1 RPGR CEP290 USH2A DNAAF2 ACBD5 BBS2 MVK CFAP221 RGR SPEF2 IFT140 CERKL C1QTNF5 CLDN19 SLC35A2 ODAD4 SEMA4A OFD1 SLC7A14 ARL6 IQCB1 C8ORF37 POGZ PRPF4 DRC1 TTC8 CC2D2A PEX12 DNAAF6 DNAH5 IFT172 WARS2 CA4 C8ORF37 TRNL1 AIPL1 CLRN1 PROM1 ATP6 TMEM67 DNAAF3 TRNT1 GAS2L2 CCDC103 ODAD1 NRL PCDH15 MKKS PMM2 CNGB1 BBS5 RHO CCDC65 PRCD KIF3B RP1 FSCN2 HGSNAT KLHL7 ATP6 CTSD DNAH11 CCNO HK1 ZNF513 ASPA PDE6A PEX19 ARL6 PEX2 CEP290 ABHD12 LRAT BEST1 RPGR PRPF31 HGSNAT CDHR1 ZNF408 CRX KIZ LRRC56 PRPF3 HYDIN USH1C MAK SDCCAG8 DHDDS IMPG2 PEX13 ND6 C8ORF37 IDH3B ARL6 PANK2 BBS12 PRPF8 SAG MTTP MERTK ATXN2 PDZD7 SPAG1 DNAAF5 BBS4 GUCA1B PPP2R3C PRPS1 GGCX CLRN1 ND5 PEX1 PEX12 KIF5A DHX38 MYO7A DNAJB13 CCDC39 TULP1 ODAD3 COQ2 OFD1 REEP6 HSPD1 ND1 TTC12 PEX3 ROM1 ROM1 MYO6 CFAP410 BBS1 ACOX1 ARL2BP NDUFA9 DNAI2 PANK2 FLVCR1 TOPORS CLRN1 DYNC2I2 CCDC28B BBS9 NME8 ODAD2 TRNV ATP6 PEX14 DNAAF4 GATA3 PCARE MDH2 BCS1L TRAF3IP1 EYS PMM2 FOXJ1 FLVCR1 MKS1 CLN3 TULP1 NPHP4 STK36 NPHP1 WDR19 USH1G PEX26 CRB1 OFD1 SRD5A3 PEX6 LRRC6 TRNW PEX6 RP9 ZMYND10 DNAI1 PEX2 CDH23 PRPF6 RPGR AHR WARS2 TRNK ARL6 CNGA1 RPE65 WHRN ADGRV1 DNAAF1 PEX7 PDE6B TMEM67 ND2 AP3B2 PEX16 PDE6G RBP3 KLHL7 SEMA4A NEK10 TTC8 DNAH1 USH2A BBS2 HMX1 CIB2 MFRP RSPH9 PCDH15 RSPH1 RP2 CFAP298 MCIDAS PEX10 IFT74 IMPDH1 PDE6G EXOSC2 BBIP1 RPL10 MAPKAPK3 TELO2 CFAP300 IFT27 RSPH3 RDH11 FDXR USH1C ND3 SH2B1
Protein Mutations 3
P23H R135W T17M
SNP 0