Genomic Map
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Target Gene Details
Entrez Gene ID: | 2272 |
Gene Name: | fragile histidine triad |
Gene Aliases: |
AP3Aase, FRA3B |
Location: |
Chr.3:59747278-61251474 on Build GRCh38 |
Assay Gene Location: | Within Intron 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FHIT | NM_001166243.2 | NP_001159715.1 | ||
| NM_001320899.1 | NP_001307828.1 | |||
| NM_001320900.1 | NP_001307829.1 | |||
| NM_001320901.1 | NP_001307830.1 | |||
| NM_002012.3 | NP_002003.1 | |||
| NR_135491.1 | ||||
| XM_017005880.1 | XP_016861369.1 | |||
| XM_017005881.1 | XP_016861370.1 | |||
| XM_017005882.1 | XP_016861371.1 | |||
| XM_017005883.1 | XP_016861372.1 | |||
| XM_017005884.1 | XP_016861373.1 | |||
| XM_017005885.1 | XP_016861374.1 | |||
| XM_017005886.1 | XP_016861375.1 | |||
| AK127931.1 | ||||
| AK289824.1 | ||||
| BC032336.1 | AAH32336.1 | |||
| DB131595.1 | ||||
| DQ120721.1 | AAZ23623.1 | |||
| KJ534835.1 | ||||
| U46922.1 | AAA99013.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv4749n100 | Chr.3:58504269 - 60219035 on Build GRCh38 | Gain |
 FAM107A
LOC339902
C3orf67
FAM3D-AS1
FHIT
ACOX2
C3orf67-AS1
FAM3D
|
| nsv1014601 | Chr.3:59680883 - 59902440 on Build GRCh38 | Loss |
FHIT
|
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Additional Information:
For this assay, SNP(s) [rs72886605] 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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