Genomic Map
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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: | Overlaps - Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC7A8 | NM_001267036.1 | NP_001253965.1 | ||
| NM_001267037.1 | NP_001253966.1 | |||
| NM_012244.3 | NP_036376.2 | |||
| NM_182728.2 | NP_877392.1 | |||
| NR_049767.1 | ||||
| AB037669.1 | BAB21519.1 | |||
| AF135830.1 | AAF05697.1 | |||
| AF171669.1 | AAF20381.1 | |||
| AK094550.1 | ||||
| AL365342.1 | ||||
| AL365344.1 | ||||
| AL365345.1 | ||||
| AL365346.1 | ||||
| AL365347.1 | ||||
| BC036825.1 | AAH36825.1 | |||
| BC052250.1 | AAH52250.1 | |||
| Y18483.1 | CAB40137.1 |
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Additional Information:
For this assay, SNP(s) [rs114646676] 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
Non-exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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