Genomic Map
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Target Gene Details
Entrez Gene ID: | 6603 |
Gene Name: | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2 |
Gene Aliases: |
BAF60B, CRACD2, PRO2451, Rsc6p |
Location: |
Chr.17:63832081-63842991 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 13 - Exon 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SMARCD2 | NM_001098426.1 | NP_001091896.1 | ||
| XM_005257604.2 | XP_005257661.2 | |||
| XM_017024967.1 | XP_016880456.1 | |||
| AF113019.1 | AAF20280.1 | |||
| AK025917.1 | ||||
| AK300939.1 | ||||
| AK303951.1 | ||||
| AK307944.1 | ||||
| BC018953.2 | AAH18953.2 | |||
| BC136322.1 | ||||
| BC142963.1 | ||||
| U66618.1 | AAC50696.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833510 | Chr.17:63767293 - 63927790 on Build GRCh38 | Loss |
 CCDC47
GH2
DDX42
PSMC5
SMARCD2
LOC107987248
TCAM1P
GH1
CSH1
FTSJ3
CSHL1
CSH2
|
| nsv517272 | Chr.17:63814307 - 64020132 on Build GRCh38 | Gain+Loss |
GH2
PSMC5
LOC107987248
GH1
CD79B
PRR29-AS1
SCN4A
FTSJ3
CSHL1
PRR29
CSH2
DDX42
SMARCD2
TCAM1P
CSH1
ICAM2
|
| nsv510720 | Chr.17:63809351 - 63908780 on Build GRCh38 | Deletion |
GH2
DDX42
PSMC5
SMARCD2
LOC107987248
TCAM1P
CSH1
FTSJ3
CSH2
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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