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MYH9 and renal failure are reported together in 3 articles.
Gene
MYH9
- HGNC
- HGNC:7579
6articles
6mentions
4variants with confirmed gene link
Most co-reported phenotypes (articles)
Reported variants (articles · ClinVar status)
Phenotype
Renal failure
523articles
523mentions
12co-reported genes shown
Most co-reported genes (articles)
Counts are literature co-mentions in SaudiVarKB, not clinical or causal assertions. Gene details: HGNC; variant status: ClinVar via dbSNP.
Publications
3 records shown · first 60Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.
PMID 32011449 | PMCID PMC7220318 | DOI 10.1097/MD.0000000000018722 · Medicine · 2020 · 6 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYH9 | “Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.” | 0.98 | hgnc_dict_v1 |
| phenotype | renal failure | “Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | UMOD | “Non-diabetic end-stage renal disease in Saudis associated with polymorphism of MYH9 gene but not UMOD gene.” | 0.98 | hgnc_dict_v1 |
| population | Saudi Arabia | “The prevalence of risk factors of chronic kidney disease in Saudi Arabia has augmented an already serious public health problem, therefore, determination of genetic variants associated with the risk of the disease presents potential screening tools that help reducing the incidence rates and promote effective disease management.The aim of the present study is to determine the association of UMOD and MYH9 genetic variants with the risk of non-diabetic end-stage renal disease (ESRD) in the Saudi population.Two single nucleotide polymorphisms (SNP), rs12917707 in gene UMOD and rs4821480 in gene MYH9 were genotyped in 154 non-diabetic ESRD Saudi patients and 123 age-matched healthy controls using Primers and Polymerase chain reaction conditions (PCR), Sanger sequencing, and TaqMan Pre-designed SNP Genotyping Assay.” | 0.95 | saudi_context_rules_v1 |
Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients.
PMID 31534799 | PMCID PMC6724424 | DOI 10.1155/2019/1095215 · International journal of nephrology · 2019 · 14 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYH9 | “Single-nucleotide polymorphisms at the proximity of SHROOM3, CST3, SLC7A9, and MYH9 genes have been associated with an increased risk of developing CKD and ESRD.” | 0.98 | hgnc_dict_v1 |
| phenotype | renal failure | “Novel Haplotype Indicator for End-Stage Renal Disease Progression among Saudi Patients.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | SHROOM3 | “Single-nucleotide polymorphisms at the proximity of SHROOM3, CST3, SLC7A9, and MYH9 genes have been associated with an increased risk of developing CKD and ESRD.” | 0.98 | hgnc_dict_v1 |
| gene | CST3 | “Single-nucleotide polymorphisms at the proximity of SHROOM3, CST3, SLC7A9, and MYH9 genes have been associated with an increased risk of developing CKD and ESRD.” | 0.98 | hgnc_dict_v1 |
Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations.
PMID 29665793 | PMCID PMC5905143 | DOI 10.1186/s12882-018-0890-9 · BMC nephrology · 2018 · 8 validated mentions
Evidence preview
| Type | Entity | Source evidence | Confidence | Extractor |
|---|---|---|---|---|
| gene | MYH9 | “METHODS: Eight genetic variants in four genes (SHROOM3, MYH9, SLC7A9, and CST3) were genotyped in 160 CKD patients and 189 ethnicity-matched healthy controls.” | 0.98 | hgnc_dict_v1 |
| phenotype | renal failure | “Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations.” | 0.93 | phenotype_alias_lexicon_v2 |
| gene | SHROOM3 | “METHODS: Eight genetic variants in four genes (SHROOM3, MYH9, SLC7A9, and CST3) were genotyped in 160 CKD patients and 189 ethnicity-matched healthy controls.” | 0.98 | hgnc_dict_v1 |
| gene | SLC7A9 | “METHODS: Eight genetic variants in four genes (SHROOM3, MYH9, SLC7A9, and CST3) were genotyped in 160 CKD patients and 189 ethnicity-matched healthy controls.” | 0.98 | hgnc_dict_v1 |