Identification of two single nucleotide polymorphisms in exon 8 of PAX2.
Mol Genet Metab
; 68(4): 507-10, 1999 Dec.
Article
in En
| MEDLINE
| ID: mdl-10607481
We estimate the allele frequencies of two single nucleotide polymorphisms (1410 C --> T) and (1521 A --> C) in the coding region of PAX2. The coding region single nucleotide polymorphisms (cSNPs) were identified by sequencing of amplimers of PAX2 exon 8 exhibiting variant migration patterns in the course of genomic DNA mutation screening from patients with renal-coloboma syndrome. Allele frequencies of the two polymorphisms were 0.94 for 1410C and 0.72 for 1521A. Cosegregation analyses of both alleles suggest that they are each in Hardy-Weinberg equilibrium and jointly in linkage equilibrium and may represent ancient polymorphisms. Characterization of PAX2 exon 8 cSNPs will serve as useful tools for mapping at the PAX2 locus.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Transcription Factors
/
Abnormalities, Multiple
/
Coloboma
/
DNA-Binding Proteins
/
Kidney
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Animals
/
Humans
/
Newborn
Language:
En
Journal:
Mol Genet Metab
Journal subject:
BIOLOGIA MOLECULAR
/
BIOQUIMICA
/
METABOLISMO
Year:
1999
Document type:
Article
Affiliation country:
United States
Country of publication:
United States