Assay Details
Target Gene Details
Entrez Gene ID: | 102724050 |
Gene Name: | uncharacterized LOC102724050 |
Gene Aliases: |
- |
Location: |
Chr.12:54353691-54467030 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC102724050 | NR_120486.1 | |||
NR_120487.1 | ||||
DA746386.1 | ||||
DA746474.1 | ||||
DA757660.1 |
Target Gene Details
Entrez Gene ID: | 25946 |
Gene Name: | zinc finger protein 385A |
Gene Aliases: |
HZF, RZF, ZFP385, ZNF385 |
Location: |
Chr.12:54369129-54391609 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 10 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
ZNF385A | NM_001130967.2 | NP_001124439.1 | ||
NM_001130968.2 | NP_001124440.1 | |||
NM_001290001.1 | NP_001276930.1 | |||
NM_001290002.1 | NP_001276931.1 | |||
NM_001290004.1 | NP_001276933.1 | |||
NM_015481.2 | NP_056296.1 | |||
XM_005268783.4 | XP_005268840.1 | |||
XM_006719342.2 | XP_006719405.1 | |||
XM_011538168.2 | XP_011536470.1 | |||
XM_011538169.2 | XP_011536471.1 | |||
XM_011538170.1 | XP_011536472.1 | |||
XM_011538171.2 | XP_011536473.1 | |||
XM_017019174.1 | XP_016874663.1 | |||
AB593085.1 | ||||
AF304052.1 | AAL08625.1 | |||
AK024404.1 | BAB14910.1 | |||
AK092724.1 | ||||
AK296564.1 | ||||
AK315613.1 | ||||
AL117462.1 | CAB55938.1 | |||
AY461717.1 | AAS19275.1 | |||
BC029752.1 | AAH29752.1 | |||
CR457327.1 | CAG33608.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv559000 | Chr.12:54343917 - 54396183 on Build GRCh38 | Loss | ITGA5 LOC102724050 GPR84 ZNF385A COPZ1 |
More Information
Additional Information:
For this assay, SNP(s) [rs114673110] 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 |