Genomic Map
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Target Gene Details
Entrez Gene ID: | 2152 |
Gene Name: | coagulation factor III, tissue factor |
Gene Aliases: |
CD142, TF, TFA |
Location: |
Chr.1:94529176-94541857 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| F3 | NM_001178096.1 | 1 | 199 | NP_001171567.1 |
| NM_001993.4 | 1 | 199 | NP_001984.1 | |
| AF487337.1 | AAO61150.1 | |||
| AK310918.1 | 1 | 98 | ||
| AK312638.1 | 1 | 95 | ||
| AY940729.1 | 1 | 101 | ||
| BC011029.1 | 1 | 146 | AAH11029.1 | |
| BT019808.1 | AAV38611.1 | |||
| CR541792.1 | CAG46591.1 | |||
| DB203987.1 | 1 | 157 | ||
| DB499288.1 | 1 | 201 | ||
| J02931.1 | 1 | 89 | AAA61150.1 | |
| M16553.1 | 1 | 53 | AAA61151.1 | |
| M27436.1 | 1 | 77 | AAA36734.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1899 | Chr.1:94534821 - 94564202 on Build GRCh38 | Insertion |
 F3
|
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Additional Information:
For this assay, SNP(s) [rs117977816] 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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