Assay Details
Target Gene Details
Entrez Gene ID: | 2208 |
Gene Name: | Fc fragment of IgE receptor II |
Gene Aliases: |
BLAST-2, CD23, CD23A, CLEC4J, FCE2, IGEBF |
Location: |
Chr.19:7688757-7702755 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FCER2 | NM_001207019.2 | 10 | 1173 | NP_001193948.2 |
NM_001220500.1 | 11 | 1309 | NP_001207429.1 | |
NM_002002.4 | 11 | 1305 | NP_001993.2 | |
XM_005272462.4 | 11 | 1910 | XP_005272519.1 | |
AK223207.1 | 11 | 1274 | BAD96927.1 | |
AK310071.1 | 10 | 1454 | ||
BC014108.2 | 11 | 1270 | AAH14108.1 | |
BC062591.1 | 11 | 1263 | AAH62591.1 | |
DB333832.1 | ||||
M14766.1 | 11 | 1277 | AAA52435.1 | |
M15059.1 | 11 | 1305 | AAA52434.1 | |
X04772.1 | 11 | 1305 | CAA28465.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv953959 | Chr.19:7669315 - 7700414 on Build GRCh38 | Deletion | MCEMP1 TRAPPC5 RETN FCER2 |
nsv833731 | Chr.19:7589114 - 7739331 on Build GRCh38 | Loss | CAMSAP3 XAB2 PCP2 CLEC4G PET100 MCEMP1 STXBP2 TRAPPC5 RETN MIR6792 FCER2 |
nsv1060887 | Chr.19:7089546 - 7861087 on Build GRCh38 | Gain | CAMSAP3 ZNF358 INSR CLEC4M CLEC4G CD209 MCOLN1 MCEMP1 STXBP2 C19orf45 LOC107985283 PNPLA6 RETN CLEC4GP1 MIR6792 LOC100128573 XAB2 PCP2 PET100 EVI5L TRAPPC5 ARHGEF18 PEX11G FCER2 |
esv2718099 | Chr.19:7688726 - 7689169 on Build GRCh38 | Deletion | FCER2 |
esv2405737 | Chr.19:7688748 - 7689152 on Build GRCh38 | Deletion | FCER2 |
nsv833732 | Chr.19:7672656 - 7871329 on Build GRCh38 | Gain | CLEC4M CLEC4G CD209 PRR36 MCEMP1 EVI5L TRAPPC5 CLEC4GP1 FCER2 |
esv2751809 | Chr.19:6896369 - 7816144 on Build GRCh38 | Gain | CAMSAP3 MBD3L4 INSR LOC729458 CLEC4G CD209 ADGRE1 MCEMP1 STXBP2 LOC107985283 PNPLA6 RETN ZNF557 LOC100128573 PCP2 ADGRE4P ARHGEF18 FCER2 ZNF358 CLEC4M MBD3L2 MBD3L3 MCOLN1 C19orf45 CLEC4GP1 MIR6792 XAB2 PET100 MBD3L5 FLJ25758 TRAPPC5 PEX11G |
nsv1061452 | Chr.19:7657750 - 7785131 on Build GRCh38 | Gain | CLEC4M CLEC4G CD209 MCEMP1 TRAPPC5 RETN FCER2 |
More Information
Additional Information:
For this assay, SNP(s) [rs72558005] 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 Exonic DGV Variation |