Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AATTCTGTCAATAGCGGCATGATCC[A/G]TAAGATGTTTTCCTGAAGGCACTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613279 | ||||||||||||||||||||
Literature Links: |
EML5 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 |
EML5 - echinoderm microtubule associated protein like 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_183387.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1866 | NP_899243.1 | |
XM_006720070.3 | 5532 | Missense Mutation | ACG,ATG | T,M 1858 | XP_006720133.1 | |
XM_011536528.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1866 | XP_011534830.1 | |
XM_011536530.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1863 | XP_011534832.1 | |
XM_011536531.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1858 | XP_011534833.1 | |
XM_011536532.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1858 | XP_011534834.1 | |
XM_011536533.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1820 | XP_011534835.1 | |
XM_011536534.2 | 5532 | Missense Mutation | ACG,ATG | T,M 1807 | XP_011534836.1 | |
XM_011536536.2 | 5532 | Intron | XP_011534838.1 | |||
XM_011536538.2 | 5532 | Intron | XP_011534840.1 | |||
XM_017021062.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1866 | XP_016876551.1 | |
XM_017021063.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1859 | XP_016876552.1 | |
XM_017021064.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1828 | XP_016876553.1 | |
XM_017021065.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1851 | XP_016876554.1 | |
XM_017021066.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1810 | XP_016876555.1 | |
XM_017021067.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1809 | XP_016876556.1 | |
XM_017021068.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1808 | XP_016876557.1 | |
XM_017021069.1 | 5532 | Missense Mutation | ACG,ATG | T,M 1807 | XP_016876558.1 | |
XM_017021070.1 | 5532 | Intron | XP_016876559.1 |
ZC3H14 - zinc finger CCCH-type containing 14 | ||||||
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There are no transcripts associated with this gene. |