Genomic Map
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Target Gene Details
Entrez Gene ID: | 51340 |
Gene Name: | crooked neck pre-mRNA splicing factor 1 |
Gene Aliases: |
CLF, CRN, Clf1, HCRN, MSTP021, SYF3 |
Location: |
Chr.20:20034361-20056046 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CRNKL1 | NM_001278625.1 | 15 | 3293 | NP_001265554.1 |
| NM_001278626.1 | 15 | 3106 | NP_001265555.1 | |
| NM_001278627.1 | 15 | 3016 | NP_001265556.1 | |
| NM_001278628.1 | 14 | 2964 | NP_001265557.1 | |
| NM_016652.5 | 15 | 3329 | NP_057736.4 | |
| AF255443.2 | 15 | 3293 | AAF65571.2 | |
| AF318303.1 | 15 | 3329 | AAK01925.1 | |
| AF318304.1 | 15 | 3106 | AAK01926.1 | |
| AF318305.1 | 15 | 3016 | AAK01927.1 | |
| AK022908.1 | 13 | 2641 | BAB14303.1 | |
| AK023246.1 | 11 | 2476 | BAB14485.1 | |
| AK026342.1 | 4 | 1350 | ||
| AL832435.1 | 14 | 2938 | CAH10656.1 |
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Additional Information:
For this assay, SNP(s) [rs75503129] 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
|
Panther Classification:
Gene Ontology Categories:
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