Genomic Map
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Target Gene Details
Entrez Gene ID: | 7401 |
Gene Name: | clarin 1 |
Gene Aliases: |
RP61, USH3, USH3A |
Location: |
Chr.3:150926163-150972999 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CLRN1 | NM_001195794.1 | NP_001182723.1 | ||
| NM_001256819.1 | NP_001243748.1 | |||
| NM_052995.2 | NP_443721.1 | |||
| NM_174878.2 | NP_777367.1 | |||
| NR_046380.2 | ||||
| AF388366.1 | AAL09581.1 | |||
| AF388368.1 | AAL09582.1 | |||
| AF482697.1 | AAN07148.1 | |||
| AF495717.1 | AAM88774.1 | |||
| BC074970.2 | AAH74970.1 | |||
| BC074971.2 | AAH74971.1 | |||
| BM666773.1 | ||||
| HM626132.1 |
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Additional Information:
For this assay, SNP(s) [rs73009136] 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
non-DGV Variation
|
Gene Ontology Categories:
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