Genomic Map
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Target Gene Details
Entrez Gene ID: | 8178 |
Gene Name: | elongation factor for RNA polymerase II |
Gene Aliases: |
C19orf17, ELL1, MEN, PPP1R68 |
Location: |
Chr.19:18442663-18522129 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ELL | NM_006532.3 | 12 | 2565 | NP_006523.1 |
| XM_017027335.1 | 13 | 2549 | XP_016882824.1 | |
| XM_017027336.1 | 8 | 2301 | XP_016882825.1 | |
| XM_017027337.1 | 7 | 1741 | XP_016882826.1 | |
| AB208794.1 | 13 | 2546 | BAD92031.1 | |
| AK225481.1 | ||||
| AK309878.1 | 3 | 918 | ||
| U16282.1 | 12 | 2505 | AAA57120.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv952420 | Chr.19:18117791 - 18476990 on Build GRCh38 | Deletion |
 PGPEP1
ELL
MAST3
PIK3R2
GDF15
RAB3A
LSM4
JUND
LOC729966
MPV17L2
ISYNA1
LOC102725254
MIR3189
SSBP4
PDE4C
LRRC25
IFI30
KIAA1683
MIR3188
|
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Additional Information:
For this assay, SNP(s) [rs80253247] 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
|
Panther Classification:
Gene Ontology Categories:
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