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The following information is based on the masked version of the consensus sequence. We have also generated data for the unmasked version of the assembly. There is also an Introduction available if you are looking for a place to get started.

All of the "Masked" resources were generated by running the RepeatMasker program on the assembled consensus sequence, and then filtering SNP loci which are determined to be too close to a repeat region for adequate primer design. This masked sequence and prettybase pair are then processed using our standard bioinformatics pipeline.



Information
Name GATA binding protein 3 isoform 2
Source PhAT
Chromosome chr10 (+) (chr10:8136673-8157170)
Accession NM_002051
SNPs 12
Indels 0
Populations 1
Subjects 0
Links [ SNPper ] [ GoldenPath ] [ Gene Image ] [ LocusLink ] [ Omim ] [ PubMed ]
Biological Significance ( See Omim for more ... )
SNP Discovery Data
Raw data
X
Prettybase
X
Refseq (FASTA)
X
Dynamic
X
SNPper Analysis
X
Flanking Sequences
X
Sequenom SNP Contexts
X
Annotated Refseq (FASTA)
X
Primers
X
Coverage
X
Archive
X
Genbank
 
Alleles
X
Allele Counts
X
Allele Frequencies
   
Genotypes
X
Genotype Counts
X
Genotype Frequencies
X
Genogram by Genotype
X
Genogram by ID
Haplotypes
X
Phase Output
    X
Phase2 Output
   
Linkage Disequlibrium
X
Combined
Additional Data ( Whitehead Dataset )
Raw data
X
Prettybase
X
Refseq (FASTA)
X
Dynamic
X
SNPper Analysis
X
Flanking Sequences
X
Sequenom SNP Contexts
X
Annotated Refseq (FASTA)
 
X
Coverage
X
Archive
X
Genbank
 
Alleles
X
Allele Counts
X
Allele Frequencies
   
Genotypes
X
Genotype Counts
X
Genotype Frequencies
X
Genogram by Genotype
X
Genogram by ID
Haplotypes
X
Phase Output
    X
Phase2 Output
   
Linkage Disequlibrium
X
Combined
Additional Data ( CAMP Dataset )
Raw data
X
Prettybase
X
Refseq (FASTA)
X
Dynamic
X
SNPper Analysis
X
Flanking Sequences
X
Sequenom SNP Contexts
X
Annotated Refseq (FASTA)
 
X
Coverage
X
Archive
X
Genbank
 
Alleles
X
Allele Counts
X
Allele Frequencies
   
Genotypes
X
Genotype Counts
X
Genotype Frequencies
X
Genogram by Genotype
X
Genogram by ID
Haplotypes
X
Phase Output
    X
Phase2 Output
   
Linkage Disequlibrium
X
Combined