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CTGTAGCACACTGGTGTCCTTGCCC[C/G]CTGTGGTCAGGGCCATGCTGTCATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600551 | ||||||||||||||||||||
Literature Links: |
EML2 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
EML2 - echinoderm microtubule associated protein like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193268.1 | 2667 | Missense Mutation | GCG,GGG | A,G 838 | NP_001180197.1 | |
NM_001193269.1 | 2667 | Missense Mutation | GCG,GGG | A,G 784 | NP_001180198.1 | |
NM_012155.2 | 2667 | Missense Mutation | GCG,GGG | A,G 637 | NP_036287.1 | |
XM_006723125.2 | 2667 | Missense Mutation | GCG,GGG | A,G 837 | XP_006723188.1 | |
XM_006723126.2 | 2667 | Missense Mutation | GCG,GGG | A,G 783 | XP_006723189.1 | |
XM_011526694.2 | 2667 | Missense Mutation | GCG,GGG | A,G 806 | XP_011524996.1 | |
XM_011526695.2 | 2667 | Missense Mutation | GCG,GGG | A,G 793 | XP_011524997.1 | |
XM_011526698.2 | 2667 | Missense Mutation | GCG,GGG | A,G 615 | XP_011525000.1 | |
XM_011526700.2 | 2667 | Missense Mutation | GCG,GGG | A,G 521 | XP_011525002.1 | |
XM_011526701.2 | 2667 | Missense Mutation | GCG,GGG | A,G 452 | XP_011525003.1 | |
XM_017026550.1 | 2667 | Missense Mutation | GCG,GGG | A,G 605 | XP_016882039.1 | |
XM_017026551.1 | 2667 | Intron | XP_016882040.1 |
GPR4 - G protein-coupled receptor 4 | ||||||
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There are no transcripts associated with this gene. |