Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 84275 |
Gene Name: | solute carrier family 25 member 33 |
Gene Aliases: |
BMSC-MCP, PNC1 |
Location: |
Chr.1:9539469-9582773 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC25A33 | NM_032315.2 | NP_115691.1 | ||
| XM_011542296.1 | XP_011540598.1 | |||
| AF495714.1 | AAM18051.1 | |||
| AJ880283.1 | CAI54244.1 | |||
| BC004991.1 | AAH04991.1 | |||
| BC073135.1 | AAH73135.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv545363 | Chr.1:9435512 - 9617795 on Build GRCh38 | Loss |
 TMEM201
LOC107985734
SLC25A33
RPL9P11
|
| nsv545377 | Chr.1:9537178 - 9542904 on Build GRCh38 | Gain |
SLC25A33
|
| nsv2076 | Chr.1:9537159 - 9571375 on Build GRCh38 | Insertion |
SLC25A33
|
| nsv1013224 | Chr.1:9380981 - 9639710 on Build GRCh38 | Gain |
TMEM201
LOC107985734
SLC25A33
RPL9P11
PIK3CD
LOC100506022
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs78601306] 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:
Back To Top