Assay Details
Target Gene Details
Entrez Gene ID: | 341880 |
Gene Name: | solute carrier family 35 member F4 |
Gene Aliases: |
C14orf36, c14_5373 |
Location: |
Chr.14:57563922-57982329 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 12 - Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC35F4 | NM_001206920.1 | NP_001193849.1 | ||
NM_001306087.1 | NP_001293016.1 | |||
XM_011536720.2 | XP_011535022.1 | |||
XM_011536721.2 | XP_011535023.1 | |||
XM_011536723.2 | XP_011535025.1 | |||
XM_011536724.2 | XP_011535026.1 | |||
XM_011536725.1 | XP_011535027.1 | |||
XM_017021258.1 | XP_016876747.1 | |||
XM_017021260.1 | XP_016876749.1 | |||
BC101318.1 | ||||
BC101320.1 | ||||
BC101321.1 | ||||
BX107164.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1046422 | Chr.14:57198718 - 58129812 on Build GRCh38 | Gain | AP5M1 C14orf37 EXOC5 SLC35F4 C14orf105 NAA30 |
nsv1043109 | Chr.14:57545677 - 57618153 on Build GRCh38 | Loss | SLC35F4 |
More Information
Additional Information:
For this assay, SNP(s) [rs113050860] 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 |