Genomic Map
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Target Gene Details
Entrez Gene ID: | 22890 |
Gene Name: | zinc finger and BTB domain containing 1 |
Gene Aliases: |
ZNF909 |
Location: |
Chr.14:64504574-64533690 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ZBTB1 | NM_001123329.1 | NP_001116801.1 | ||
| NM_014950.2 | NP_055765.2 | |||
| XM_005267410.1 | XP_005267467.1 | |||
| XM_011536566.2 | XP_011534868.1 | |||
| XM_011536568.2 | XP_011534870.1 | |||
| XM_017021094.1 | XP_016876583.1 | |||
| XM_017021095.1 | XP_016876584.1 | |||
| AB023214.1 | ||||
| AK291743.1 | ||||
| BC050719.1 | AAH50719.1 | |||
| BX248777.1 | CAD66584.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv521823 | Chr.14:64502624 - 64528976 on Build GRCh38 | Loss |
 ZBTB25
ZBTB1
LOC102723809
|
| esv3634753 | Chr.14:64507850 - 64510486 on Build GRCh38 | Loss |
ZBTB1
|
| esv2748779 | Chr.14:63663324 - 66595809 on Build GRCh38 | Deletion |
ZBTB25
CHURC1-FNTB
SPTB
LOC102723809
MIR4708
MIR4706
LINC00238
SGPP1
LOC100506321
MAX
MIR548H1
AKAP5
MIR625
ESR2
GPHN
FUT8
LOC100128233
ZBTB1
FNTB
HSPA2
GPX2
MTHFD1
FUT8-AS1
RAB15
TEX21P
CHURC1
SYNE2
PPP1R36
PLEKHG3
MIR7855
|
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Additional Information:
For this assay, SNP(s) [rs74056444] 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
|
Panther Classification:
Gene Ontology Categories:
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