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OXTR
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 167055
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Literature Links: |
OXTR PubMed Links | ||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| Applied Biosystems® |
|---|
| Caucasian - Not Available |
| African American - Not Available |
| Chinese - Not Available |
| Japanese - Not Available |
| OXTR - oxytocin receptor | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000916.3 | Intron | NP_000907.2 | ||||
| XM_011533762.2 | Intron | XP_011532064.1 | ||||
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Additional Information:
For this assay, SNP(s) [rs75943879] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Panther Classification:
Gene Ontology Categories:
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