Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610073 MIM: 600258 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ORMDL1 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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ORMDL1 - ORMDL sphingolipid biosynthesis regulator 1 | ||||||
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There are no transcripts associated with this gene. |
PMS1 - PMS1 homolog 1, mismatch repair system component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000534.4 | Intron | NP_000525.1 | ||||
NM_001128143.1 | Intron | NP_001121615.1 | ||||
NM_001128144.1 | Intron | NP_001121616.1 | ||||
NM_001289408.1 | Intron | NP_001276337.1 | ||||
NM_001289409.1 | Intron | NP_001276338.1 | ||||
NM_001321044.1 | Intron | NP_001307973.1 | ||||
NM_001321045.1 | Intron | NP_001307974.1 | ||||
NM_001321046.1 | Intron | NP_001307975.1 | ||||
NM_001321047.1 | Intron | NP_001307976.1 | ||||
NM_001321048.1 | Intron | NP_001307977.1 | ||||
NM_001321049.1 | Intron | NP_001307978.1 | ||||
NM_001321051.1 | Intron | NP_001307980.1 | ||||
XM_006712596.1 | Intron | XP_006712659.1 | ||||
XM_011511356.2 | Intron | XP_011509658.1 | ||||
XM_017004344.1 | Intron | XP_016859833.1 | ||||
XM_017004345.1 | Intron | XP_016859834.1 | ||||
XM_017004346.1 | Intron | XP_016859835.1 | ||||
XM_017004347.1 | Intron | XP_016859836.1 | ||||
XM_017004348.1 | Intron | XP_016859837.1 | ||||
XM_017004349.1 | Intron | XP_016859838.1 | ||||
XM_017004350.1 | Intron | XP_016859839.1 | ||||
XM_017004351.1 | Intron | XP_016859840.1 |
Set Membership: |
HapMap |