Assay Details
Target Gene Details
Entrez Gene ID: | 256297 |
Gene Name: | pancreas specific transcription factor, 1a |
Gene Aliases: |
PACA, PAGEN2, PTF1-p48, bHLHa29 |
Location: |
Chr.10:23192531-23194252 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PTF1A | NM_178161.2 | 1 | 153 | NP_835455.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv825302 | Chr.10:23168093 - 23208400 on Build GRCh38 | Gain | C10orf67 PTF1A |
nsv1068293 | Chr.10:23189170 - 23194971 on Build GRCh38 | Deletion | PTF1A |
nsv825301 | Chr.10:23151675 - 23216917 on Build GRCh38 | Gain | C10orf67 PTF1A |
nsv831810 | Chr.10:23156718 - 23316341 on Build GRCh38 | Gain | C10orf67 PTF1A |
More Information
Additional Information:
For this assay, SNP(s) [rs117678424] 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 DGV Variation |