Assay Details
Target Gene Details
Entrez Gene ID: | 54932 |
Gene Name: | exonuclease 3'-5' domain containing 3 |
Gene Aliases: |
mut-7 |
Location: |
Chr.9:137306894-137423262 on Build GRCh38 |
Assay Gene Location: | Within Intron 27 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
EXD3 | NM_017820.4 | NP_060290.3 | ||
XM_011518810.1 | XP_011517112.1 | |||
XM_011518814.1 | XP_011517116.1 | |||
XM_011518815.1 | XP_011517117.1 | |||
XM_017014861.1 | XP_016870350.1 | |||
XM_017014862.1 | XP_016870351.1 | |||
XM_017014863.1 | XP_016870352.1 | |||
XM_017014864.1 | XP_016870353.1 | |||
XM_017014865.1 | XP_016870354.1 | |||
XM_017014866.1 | XP_016870355.1 | |||
XM_017014867.1 | XP_016870356.1 | |||
AB061798.1 | BAC10986.1 | |||
AK055004.1 | BAB70838.1 | |||
AK094438.1 | BAC04356.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv13009n54 | Chr.9:137173890 - 137327859 on Build GRCh38 | Loss |
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dgv13011n54 | Chr.9:137223996 - 137338927 on Build GRCh38 | Loss |
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esv2759721 | Chr.9:137303332 - 137447299 on Build GRCh38 | Loss |
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nsv524322 | Chr.9:136795692 - 137482216 on Build GRCh38 | Loss |
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nsv951207 | Chr.9:137136949 - 137379148 on Build GRCh38 | Deletion |
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nsv6770 | Chr.9:137316337 - 137347440 on Build GRCh38 | Insertion |
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nsv1161918 | Chr.9:137118319 - 137438026 on Build GRCh38 | Duplication |
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nsv1037407 | Chr.9:137275904 - 137361369 on Build GRCh38 | Gain |
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esv2422220 | Chr.9:136584135 - 137350098 on Build GRCh38 | Deletion |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
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More Information
Additional Information:
For this assay, SNP(s) [rs144589250] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
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Gene Ontology Categories:
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