IthaID: 2638
Names and Sequences
| Functionality: | Disease modifying mutation | Pathogenicity: | N/A |
|---|---|---|---|
| Common Name: | rs1557529 | HGVS Name: | NG_011884.2:g.83535T>C |
Context nucleotide sequence:
TCCGGAGCACAGGCTAACCCCATGC [A/G] TGGAAAAGTCAGAAAACGTGAAGAC (Strand: +)
Also known as:
Comments: SNP associated with proteinuria in individuals with sickle cell disease acquired from the Duke University Medical Center, the University of North Carolina at Chapel Hill, the East Carolina University and the Emory University Sickle Cell Centers (n=521).
We follow the HGVS sequence variant nomenclature and IUPAC standards.
External Links
Phenotype
| Allele Phenotype (Cis): | N/A |
|---|---|
| Allele Phenotype (Trans): | N/A |
| Associated Phenotypes: | Proteinuria [HP:0000093] |
Location
| Chromosome: | 22 |
|---|---|
| Locus: | NG_011884.2 |
| Locus Location: | 83535 |
| Size: | 1 bp |
| Located at: | MYH9 |
| Specific Location: | Intron 14 |
Other details
| Type of Mutation: | Point-Mutation(Substitution) |
|---|---|
| Effect on Gene/Protein Function: | N/A |
| Ethnic Origin: | African American |
| Molecular mechanism: | N/A |
| Inheritance: | Quantitative trait |
| DNA Sequence Determined: | Yes |
In silico pathogenicity prediction
Publications / Origin
- Ashley-Koch AE, Okocha EC, Garrett ME, Soldano K, De Castro LM, Jonassaint JC, Orringer EP, Eckman JR, Telen MJ, MYH9 and APOL1 are both associated with sickle cell disease nephropathy., Br. J. Haematol. , 155(3), 386-94, 2011
Created on 2016-05-10 15:38:26,
Last reviewed on (Show full history)
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