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TTCAATTGTGTGCAGCTTCAAGTAG[C/T]GGCATTCCACGCTGCCCATGCCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611165 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DPRX PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DPRX - divergent-paired related homeobox | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012728.1 | Intron | NP_001012746.1 | ||||
XM_011527011.2 | Intron | XP_011525313.1 | ||||
XM_011527012.2 | Intron | XP_011525314.1 |
LOC284379 - solute carrier family 7 member 3 pseudogene | ||||||
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There are no transcripts associated with this gene. |