Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131370 MIM: 176610 MIM: 610431 MIM: 610056 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ENO3 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
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CEPH (CEU)
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EAS
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African American
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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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ENO3 - enolase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193503.1 | 736 | Intron | NP_001180432.1 | |||
NM_001976.4 | 736 | Intron | NP_001967.3 | |||
NM_053013.3 | 736 | Intron | NP_443739.3 | |||
XM_005256521.2 | 736 | Missense Mutation | AAT,AGT | N,S 80 | XP_005256578.1 | |
XM_011523729.1 | 736 | Missense Mutation | AAT,AGT | N,S 71 | XP_011522031.1 | |
XM_017024346.1 | 736 | Missense Mutation | AAT,AGT | N,S 71 | XP_016879835.1 |
PFN1 - profilin 1 | ||||||
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There are no transcripts associated with this gene. |
RNF167 - ring finger protein 167 | ||||||
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There are no transcripts associated with this gene. |
SPAG7 - sperm associated antigen 7 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap Validated |