Assay Details
Target Gene Details
Entrez Gene ID: | 6503 |
Gene Name: | Src-like-adaptor |
Gene Aliases: |
SLA1, SLAP |
Location: |
Chr.8:133036728-133103360 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLA | NM_001045556.2 | NP_001039021.1 | ||
NM_001045557.2 | NP_001039022.2 | |||
NM_001282964.1 | NP_001269893.1 | |||
NM_001282965.1 | NP_001269894.1 | |||
XM_017013739.1 | XP_016869228.1 | |||
AK297423.1 | ||||
AK297519.1 | ||||
AK309401.1 | ||||
AK312584.1 | ||||
BX648382.1 | ||||
DA483212.1 | ||||
DA522819.1 | ||||
DC313073.1 | ||||
U30473.1 | AAC50357.1 | |||
U44403.1 | AAC27662.1 |
Target Gene Details
Entrez Gene ID: | 7038 |
Gene Name: | thyroglobulin |
Gene Aliases: |
AITD3, TGN |
Location: |
Chr.8:132866943-133134902 on Build GRCh38 |
Assay Gene Location: | Within Exon 46 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TG | NM_003235.4 | 42 | 7326 | NP_003226.4 |
XM_005251038.4 | 41 | 7151 | XP_005251095.1 | |
XM_006716622.3 | 41 | 7280 | XP_006716685.1 | |
XM_017013793.1 | 41 | 7277 | XP_016869282.1 | |
XM_017013794.1 | 42 | 7343 | XP_016869283.1 | |
XM_017013795.1 | 41 | 7172 | XP_016869284.1 | |
XM_017013796.1 | 41 | 7124 | XP_016869285.1 | |
XM_017013797.1 | 41 | 7237 | XP_016869286.1 | |
AB209159.1 | 29 | 3940 | BAD92396.1 | |
AK299197.1 | 13 | 2002 | ||
AK303666.1 | ||||
AK303667.1 | 21 | 2651 | ||
BC127887.1 | 9 | 1172 | ||
BC140933.1 | 42 | 7319 | ||
U93033.2 | 42 | 7285 | AAC51924.1 | |
X05615.1 | 42 | 7323 | CAA29104.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv465818 | Chr.8:133093077 - 133122429 on Build GRCh38 | Loss | TG SLA |
nsv482993 | Chr.8:132994656 - 133137835 on Build GRCh38 | Loss | MIR7848 TG SLA |
More Information
Additional Information:
For this assay, SNP(s) [rs73354644] 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 Exonic Intronic Non-exonic DGV Variation |