Assay Details
Target Gene Details
Entrez Gene ID: | 54868 |
Gene Name: | transmembrane protein 104 |
Gene Aliases: |
- |
Location: |
Chr.17:74776483-74839783 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TMEM104 | NM_001321264.1 | NP_001308193.1 | ||
NM_017728.3 | NP_060198.3 | |||
XM_006721963.1 | XP_006722026.1 | |||
XM_017024797.1 | XP_016880286.1 | |||
XM_017024798.1 | XP_016880287.1 | |||
XM_017024799.1 | XP_016880288.1 | |||
AK000262.1 | BAA91039.1 | |||
AK074029.1 | ||||
AK291159.1 | ||||
AK296621.1 | ||||
BC037278.1 | AAH37278.1 | |||
DN999695.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv952367 | Chr.17:74751962 - 74961105 on Build GRCh38 | Deletion | HID1 GRIN2C FADS6 SLC9A3R1 USH1G OTOP2 OTOP3 NAT9 FDXR TMEM104 |
nsv457907 | Chr.17:74778036 - 74818437 on Build GRCh38 | Loss | TMEM104 |
More Information
Additional Information:
For this assay, SNP(s) [rs112031124] 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: |
Intragenic Intronic Non-exonic DGV Variation |