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Search Thermo Fisher Scientific
GTCCATTCACATTTCTTATCTCTGA[A/C]CAAGGGGCAATTTGAAATTCGATAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615532 MIM: 186977 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ERMARD 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) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ERMARD - ER membrane associated RNA degradation | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278531.1 | 1378 | Missense Mutation | AAC,ACC | N,T 86 | NP_001265460.1 | |
NM_001278532.1 | 1378 | UTR 5 | NP_001265461.1 | |||
NM_001278533.1 | 1378 | Missense Mutation | AAC,ACC | N,T 86 | NP_001265462.1 | |
NM_018341.2 | 1378 | Missense Mutation | AAC,ACC | N,T 86 | NP_060811.1 | |
XM_011535938.2 | 1378 | Missense Mutation | AAC,ACC | N,T 86 | XP_011534240.1 | |
XM_011535939.2 | 1378 | UTR 5 | XP_011534241.1 | |||
XM_011535940.2 | 1378 | UTR 5 | XP_011534242.1 | |||
XM_017011027.1 | 1378 | UTR 5 | XP_016866516.1 | |||
XM_017011028.1 | 1378 | UTR 5 | XP_016866517.1 | |||
XM_017011029.1 | 1378 | UTR 5 | XP_016866518.1 | |||
XM_017011030.1 | 1378 | UTR 5 | XP_016866519.1 | |||
XM_017011031.1 | 1378 | UTR 5 | XP_016866520.1 | |||
XM_017011032.1 | 1378 | UTR 5 | XP_016866521.1 | |||
XM_017011033.1 | 1378 | UTR 5 | XP_016866522.1 |
TCTE3 - t-complex-associated-testis-expressed 3 | ||||||
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There are no transcripts associated with this gene. |