Genomic Map
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Target Gene Details
Entrez Gene ID: | 8462 |
Gene Name: | Kruppel like factor 11 |
Gene Aliases: |
FKLF, FKLF1, MODY7, TIEG2, Tieg3 |
Location: |
Chr.2:10043555-10054836 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KLF11 | NM_001177716.1 | 4 | 2037 | NP_001171187.1 |
| NM_001177718.1 | 4 | 2185 | NP_001171189.1 | |
| NM_003597.4 | 4 | 2182 | NP_003588.1 | |
| AK002186.1 | 1 | 242 | ||
| AK289816.1 | ||||
| AK302880.1 | ||||
| BC063286.1 | 4 | 2182 | AAH63286.1 | |
| BQ881155.1 | 1 | 210 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv828308 | Chr.2:10035398 - 10060201 on Build GRCh38 | Gain |
 LOC101929882
KLF11
CYS1
|
| nsv828297 | Chr.2:9969170 - 10096205 on Build GRCh38 | Loss |
LOC101929882
KLF11
GRHL1
CYS1
|
| dgv3715n100 | Chr.2:10014833 - 10135998 on Build GRCh38 | Gain |
RRM2
LOC101929882
KLF11
CYS1
|
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Additional Information:
For this assay, SNP(s) [rs72786612] 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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