Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614179 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ISLR2 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)
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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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ISLR2 - immunoglobulin superfamily containing leucine rich repeat 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130136.1 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | NP_001123608.1 | |
NM_001130137.1 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | NP_001123609.1 | |
NM_001130138.1 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | NP_001123610.1 | |
NM_020851.2 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | NP_065902.1 | |
XM_011521840.2 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | XP_011520142.1 | |
XM_011521841.1 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | XP_011520143.1 | |
XM_017022446.1 | 1018 | Missense Mutation | TCT,TTT | S,F 137 | XP_016877935.1 |
LOC283731 - uncharacterized LOC283731 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |