Genomic Map
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Target Gene Details
Entrez Gene ID: | 196913 |
Gene Name: | long intergenic non-protein coding RNA 1599 |
Gene Aliases: |
C14orf183 |
Location: |
Chr.14:50007313-50105043 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LINC01599 | NR_131171.1 | |||
| BQ027525.1 | ||||
| BU927649.1 | ||||
| DA856251.1 | ||||
| T90102.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv564835 | Chr.14:50024482 - 50439753 on Build GRCh38 | Gain |
 MIR4504
LINC01599
CDKL1
MAP4K5
SOS2
L2HGDH
VCPKMT
ATP5S
|
| nsv1048869 | Chr.14:50020658 - 50056451 on Build GRCh38 | Gain |
LINC01599
|
| esv28926 | Chr.14:49426970 - 50475809 on Build GRCh38 | Gain+Loss |
RPL36AL
LRR1
DNAAF2
MIR6076
LINC01588
MAP4K5
POLE2
LOC100506446
SOS2
KLHDC1
MGAT2
VCPKMT
ATP5S
ARF6
MIR4504
LINC01599
RN7SL2
CDKL1
NEMF
L2HGDH
RPS29
KLHDC2
LOC100288910
RN7SL1
|
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Additional Information:
For this assay, SNP(s) [rs116141338] 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
DGV Variation
|
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