Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608791 MIM: 600691 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
NXNL1 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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NXNL1 - nucleoredoxin-like 1 | ||||||
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There are no transcripts associated with this gene. |
SLC27A1 - solute carrier family 27 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_198580.2 | Intron | NP_940982.1 | ||||
XM_011528000.1 | Intron | XP_011526302.1 | ||||
XM_011528001.2 | Intron | XP_011526303.1 | ||||
XM_011528002.2 | Intron | XP_011526304.1 | ||||
XM_011528003.2 | Intron | XP_011526305.1 | ||||
XM_017026781.1 | Intron | XP_016882270.1 |
Set Membership: |
HapMap |