Assay Details
Target Gene Details
Entrez Gene ID: | 933 |
Gene Name: | CD22 molecule |
Gene Aliases: |
SIGLEC-2, SIGLEC2 |
Location: |
Chr.19:35329166-35347361 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 1 - Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CD22 | NM_001185099.1 | NP_001172028.1 | ||
NM_001185100.1 | NP_001172029.1 | |||
NM_001185101.1 | NP_001172030.1 | |||
NM_001278417.1 | NP_001265346.1 | |||
NM_001771.3 | NP_001762.2 | |||
AK026467.1 | BAB15489.1 | |||
AK225625.1 | ||||
AK225694.1 | ||||
AK301177.1 | ||||
BC109306.1 | AAI09307.1 | |||
CF138699.1 | ||||
DA931592.1 | ||||
DA989528.1 | ||||
X52785.1 | CAA36988.1 | |||
X59350.1 | CAA42006.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833810 | Chr.19:35291685 - 35481057 on Build GRCh38 | Gain | FFAR1 FFAR3 FFAR2 MAG CD22 MIR5196 LINC01531 |
esv2758758 | Chr.19:35220175 - 35396211 on Build GRCh38 | Loss | FFAR1 FFAR3 MAG FAM187B HAMP CD22 USF2 MIR5196 LSR |
nsv510765 | Chr.19:35217323 - 35399766 on Build GRCh38 | Deletion | FFAR1 FFAR3 MAG FAM187B HAMP CD22 USF2 MIR5196 LSR |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |