Assay Details
Target Gene Details
Entrez Gene ID: | 137695 |
Gene Name: | transmembrane protein 68 |
Gene Aliases: |
- |
Location: |
Chr.8:55738744-55773407 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TMEM68 | NM_001286657.1 | NP_001273586.1 | ||
NM_001286661.1 | NP_001273590.1 | |||
NM_152417.2 | NP_689630.1 | |||
XM_005251150.1 | XP_005251207.1 | |||
XM_011517454.1 | XP_011515756.1 | |||
XM_011517455.2 | XP_011515757.1 | |||
XM_017013040.1 | XP_016868529.1 | |||
AK056932.1 | BAB71312.1 | |||
AL832935.1 | CAH56335.1 | |||
CN272366.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv459n21 | Chr.8:55676869 - 56030580 on Build GRCh38 | Gain |
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nsv527341 | Chr.8:55679732 - 55895699 on Build GRCh38 | Gain |
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esv2422388 | Chr.8:55707094 - 55812437 on Build GRCh38 | Duplication |
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nsv611392 | Chr.8:55741553 - 55878302 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs78883741] 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:
