Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 132880 MIM: 610675 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
NR2F6 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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NR2F6 - nuclear receptor subfamily 2 group F member 6 | ||||||
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There are no transcripts associated with this gene. |
OCEL1 - occludin/ELL domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024578.2 | 416 | Silent Mutation | GCC,GCT | A,A 124 | NP_078854.1 | |
XM_005260079.2 | 416 | Silent Mutation | GCC,GCT | A,A 68 | XP_005260136.1 | |
XM_006722899.3 | 416 | Silent Mutation | GCC,GCT | A,A 124 | XP_006722962.1 | |
XM_017027306.1 | 416 | Silent Mutation | GCC,GCT | A,A 68 | XP_016882795.1 |
USE1 - unconventional SNARE in the ER 1 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |