Genomic Map
Back To TopAssay 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 Intron 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FCER2 | NM_001207019.2 | NP_001193948.2 | ||
| NM_001220500.1 | NP_001207429.1 | |||
| NM_002002.4 | NP_001993.2 | |||
| XM_005272462.4 | XP_005272519.1 | |||
| AK223207.1 | BAD96927.1 | |||
| AK310071.1 | ||||
| BC014108.2 | AAH14108.1 | |||
| BC062591.1 | AAH62591.1 | |||
| M14766.1 | AAA52435.1 | |||
| M15059.1 | AAA52434.1 | |||
| X04772.1 | CAA28465.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833731 | Chr.19:7589114 - 7739331 on Build GRCh38 | Loss |
 PET100
XAB2
RETN
FCER2
PCP2
CAMSAP3
MCEMP1
MIR6792
CLEC4G
STXBP2
TRAPPC5
|
| dgv6251n54 | Chr.19:7692028 - 7694790 on Build GRCh38 | Loss |
FCER2
|
| nsv833732 | Chr.19:7672656 - 7871329 on Build GRCh38 | Gain |
FCER2
CD209
CLEC4M
MCEMP1
CLEC4G
EVI5L
PRR36
TRAPPC5
CLEC4GP1
|
| nsv1061452 | Chr.19:7657750 - 7785131 on Build GRCh38 | Gain |
RETN
FCER2
CD209
CLEC4M
MCEMP1
CLEC4G
TRAPPC5
|
| nsv953959 | Chr.19:7669315 - 7700414 on Build GRCh38 | Deletion |
RETN
FCER2
MCEMP1
TRAPPC5
|
| nsv1060887 | Chr.19:7089546 - 7861087 on Build GRCh38 | Gain |
PET100
PEX11G
C19orf45
CD209
ZNF358
MCOLN1
MIR6792
ARHGEF18
CLEC4G
LOC100128573
LOC107985283
INSR
XAB2
RETN
FCER2
PCP2
CAMSAP3
CLEC4M
PNPLA6
MCEMP1
EVI5L
STXBP2
TRAPPC5
CLEC4GP1
|
| dgv6248n54 | Chr.19:7690993 - 7693584 on Build GRCh38 | Loss |
FCER2
|
| esv3388356 | Chr.19:7690666 - 7693264 on Build GRCh38 | Duplication |
FCER2
|
| dgv502e201 | Chr.19:7691733 - 7692739 on Build GRCh38 | Deletion |
FCER2
|
| dgv6250n54 | Chr.19:7691712 - 7693584 on Build GRCh38 | Loss |
FCER2
|
| esv2751809 | Chr.19:6896369 - 7816144 on Build GRCh38 | Gain |
PET100
PEX11G
CD209
ZNF358
ARHGEF18
CLEC4G
LOC107985283
MBD3L4
RETN
FCER2
PCP2
CAMSAP3
PNPLA6
MBD3L2
FLJ25758
ADGRE1
STXBP2
MBD3L5
C19orf45
ZNF557
LOC729458
MCOLN1
MIR6792
LOC100128573
INSR
XAB2
ADGRE4P
CLEC4M
MCEMP1
MBD3L3
TRAPPC5
CLEC4GP1
|
| esv26340 | Chr.19:7690078 - 7698176 on Build GRCh38 | Gain |
FCER2
|
| nsv578522 | Chr.19:7691153 - 7694144 on Build GRCh38 | Loss |
FCER2
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs72998491,rs72998492] 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