Assay Details
Target Gene Details
Entrez Gene ID: | 29883 |
Gene Name: | CCR4-NOT transcription complex subunit 7 |
Gene Aliases: |
CAF-1, CAF1, Caf1a, hCAF-1 |
Location: |
Chr.8:17226030-17246909 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CNOT7 | NM_001322087.1 | 7 | 1274 | NP_001309016.1 |
NM_001322088.1 | 6 | 1059 | NP_001309017.1 | |
NM_001322089.1 | 6 | 1265 | NP_001309018.1 | |
NM_001322090.1 | NP_001309019.1 | |||
NM_001322091.1 | NP_001309020.1 | |||
NM_001322092.1 | NP_001309021.1 | |||
NM_001322093.1 | NP_001309022.1 | |||
NM_001322094.1 | NP_001309023.1 | |||
NM_001322095.1 | NP_001309024.1 | |||
NM_001322096.1 | NP_001309025.1 | |||
NM_001322097.1 | NP_001309026.1 | |||
NM_001322098.1 | 7 | 1303 | NP_001309027.1 | |
NM_001322099.1 | 7 | 1380 | NP_001309028.1 | |
NM_001322100.1 | 8 | 1238 | NP_001309029.1 | |
NM_013354.6 | NP_037486.2 | |||
NM_054026.3 | 6 | 1199 | NP_473367.2 | |
XM_005273481.2 | XP_005273538.1 | |||
AA134869.1 | ||||
AF086915.1 | AAP97145.1 | |||
AK001209.1 | ||||
AK021808.1 | ||||
AK023466.1 | 6 | 1168 | ||
AK225893.1 | ||||
AL528251.3 | ||||
AL833642.1 | ||||
BC007315.2 | AAH07315.1 | |||
BC060852.1 | AAH60852.1 | |||
BC070187.1 | AAH70187.1 | |||
BI094365.1 | 2 | 309 | ||
BT006685.1 | AAP35331.1 | |||
DA695885.1 | ||||
L46722.1 | AAF01500.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831244 | Chr.8:17105917 - 17270710 on Build GRCh38 | Gain | LOC105379298 CNOT7 ZDHHC2 MICU3 VPS37A |
More Information
Additional Information:
For this assay, SNP(s) [rs77250415] 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 |