Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 9942 |
Gene Name: | xylulokinase |
Gene Aliases: |
- |
Location: |
Chr.3:38346760-38453041 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 4 - Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| XYLB | NM_005108.3 | NP_005099.2 | ||
| XM_011534325.2 | XP_011532627.1 | |||
| XM_011534327.1 | XP_011532629.1 | |||
| XM_011534328.2 | XP_011532630.1 | |||
| XM_011534329.1 | XP_011532631.1 | |||
| XM_011534330.2 | XP_011532632.1 | |||
| XM_017007595.1 | XP_016863084.1 | |||
| XM_017007596.1 | XP_016863085.1 | |||
| XM_017007598.1 | XP_016863087.1 | |||
| XM_017007599.1 | XP_016863088.1 | |||
| XM_017007600.1 | XP_016863089.1 | |||
| AB015046.1 | BAA31527.1 | |||
| AK025728.1 | ||||
| AK293325.1 | ||||
| AK314386.1 | ||||
| BC030231.2 | AAH30231.1 | |||
| BC137076.1 | ||||
| BC137080.1 | ||||
| BI090475.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv238024 | Chr.3:38358218 - 38360780 on Build GRCh38 | Deletion |
 XYLB
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs79369741] 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
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top