Assay Details
Target Gene Details
Entrez Gene ID: | 23428 |
Gene Name: | solute carrier family 7 member 8 |
Gene Aliases: |
LAT2, LPI-PC1 |
Location: |
Chr.14:23125295-23183660 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC7A8 | NM_001267036.1 | 9 | 2703 | NP_001253965.1 |
NM_001267037.1 | 8 | 2448 | NP_001253966.1 | |
NM_012244.3 | 11 | 3664 | NP_036376.2 | |
NM_182728.2 | 9 | 2602 | NP_877392.1 | |
NR_049767.1 | 7 | 2643 | ||
AB037669.1 | 11 | 3627 | BAB21519.1 | |
AF135830.1 | 7 | 2245 | AAF05697.1 | |
AF171669.1 | 11 | 3141 | AAF20381.1 | |
AK094550.1 | 3 | 2149 | ||
AL365342.1 | 6 | 2996 | ||
AL365344.1 | 5 | 1979 | ||
AL365345.1 | 7 | 2281 | ||
AL365346.1 | 3 | 1867 | ||
AL365347.1 | 2 | 1255 | ||
BC036825.1 | 7 | 2494 | AAH36825.1 | |
BC052250.1 | 11 | 2947 | AAH52250.1 | |
Y18483.1 | 11 | 3648 | CAB40137.1 |
More Information
Additional Information:
For this assay, SNP(s) [rs117878694] 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 non-DGV Variation |