Genomic Map
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Target Gene Details
Entrez Gene ID: | 54982 |
Gene Name: | ceroid-lipofuscinosis, neuronal 6, late infantile, variant |
Gene Aliases: |
CLN4A, HsT18960, nclf |
Location: |
Chr.15:68206992-68229742 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CLN6 | NM_017882.2 | NP_060352.1 | ||
| AK000568.1 | BAA91260.1 | |||
| AK027604.1 | BAB55226.1 | |||
| AK074753.1 | BAC11181.1 | |||
| AK291175.1 | ||||
| AK293155.1 | ||||
| AK293197.1 | ||||
| BC010849.1 | AAH10849.1 | |||
| BC013130.1 | AAH13130.1 | |||
| CR457244.1 | CAG33525.1 | |||
| KU178671.1 | ||||
| KU178672.1 | ||||
| KU178673.1 | ||||
| KU178674.1 |
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Additional Information:
For this assay, SNP(s) [rs116956347] 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
|
Gene Ontology Categories:
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