Assay Details
Target Gene Details
Entrez Gene ID: | 54733 |
Gene Name: | solute carrier family 35 member F2 |
Gene Aliases: |
HSNOV1 |
Location: |
Chr.11:107790991-107859188 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC35F2 | NM_017515.4 | NP_059985.2 | ||
AK023080.1 | BAB14394.1 | |||
AK128062.1 | BAC87256.1 | |||
AK300582.1 | ||||
AL833969.1 | CAI46204.1 | |||
BC039195.2 | AAH39195.1 | |||
BC048302.1 | AAH48302.1 | |||
DA840333.1 | ||||
DC352180.1 | ||||
X99961.1 | CAA68226.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv2175n54 | Chr.11:107773570 - 107826907 on Build GRCh38 | Loss | SLC35F2 |
dgv1277n100 | Chr.11:107816082 - 107862772 on Build GRCh38 | Gain | SLC35F2 |
nsv1035229 | Chr.11:107783005 - 107846464 on Build GRCh38 | Gain | SLC35F2 |
esv3627655 | Chr.11:107740978 - 107953197 on Build GRCh38 | Gain | SLC35F2 RAB39A |
nsv468867 | Chr.11:107778300 - 107826907 on Build GRCh38 | Loss | SLC35F2 |
dgv1274n100 | Chr.11:107597955 - 108083284 on Build GRCh38 | Gain | CUL5 SLN SLC35F2 RAB39A ELMOD1 |
nsv521771 | Chr.11:107719609 - 108033920 on Build GRCh38 | Gain | CUL5 SLC35F2 RAB39A |
dgv1276n100 | Chr.11:107693548 - 108059223 on Build GRCh38 | Gain | CUL5 SLN SLC35F2 RAB39A |
dgv230e214 | Chr.11:107682939 - 107838250 on Build GRCh38 | Gain | SLN SLC35F2 |
More Information
Additional Information:
For this assay, SNP(s) [rs73001550] 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 |