Genomic Map
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Target Gene Details
Entrez Gene ID: | 64943 |
Gene Name: | 5'-nucleotidase domain containing 2 |
Gene Aliases: |
- |
Location: |
Chr.3:52524369-52535077 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 17 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NT5DC2 | NM_001134231.1 | NP_001127703.1 | ||
| NM_022908.2 | NP_075059.1 | |||
| XM_005265406.2 | XP_005265463.1 | |||
| XM_006713303.3 | XP_006713366.1 | |||
| XM_006713305.2 | XP_006713368.1 | |||
| AF131781.1 | AAD20044.1 | |||
| AK022504.1 | BAB14064.1 | |||
| AK023995.1 | BAB14763.1 | |||
| AK092469.1 | ||||
| BC014550.1 | AAH14550.1 | |||
| BM982658.1 |
Target Gene Details
Entrez Gene ID: | 23166 |
Gene Name: | stabilin 1 |
Gene Aliases: |
CLEVER-1, FEEL-1, FELE-1, FEX1, SCARH2, STAB-1 |
Location: |
Chr.3:52495338-52524496 on Build GRCh38 |
Assay Gene Location: | Within Exon 69 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| STAB1 | NM_015136.2 | 69 | 7829 | NP_055951.2 |
| XM_005264973.3 | 68 | 7906 | XP_005265030.1 | |
| XM_005264974.2 | 69 | 7828 | XP_005265031.1 | |
| XM_017005998.1 | 68 | 7966 | XP_016861487.1 | |
| XM_017005999.1 | 69 | 7891 | XP_016861488.1 | |
| XM_017006000.1 | 69 | 7888 | XP_016861489.1 | |
| XM_017006001.1 | 67 | 7870 | XP_016861490.1 | |
| XM_017006002.1 | 67 | 7816 | XP_016861491.1 | |
| XM_017006003.1 | 68 | 7786 | XP_016861492.1 | |
| AB052956.1 | 69 | 7816 | BAC15606.1 | |
| AJ275213.1 | 69 | 7785 | CAB61827.1 | |
| AK091600.1 | 19 | 2768 | ||
| AK093774.1 | 12 | 2065 | ||
| AK097061.1 | ||||
| BC150250.1 | 69 | 7835 | ||
| BI001474.1 | 2 | 180 | ||
| D87433.2 | 69 | 7814 | ||
| DQ786774.1 | 69 | 7779 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv954862 | Chr.3:52476885 - 52530884 on Build GRCh38 | Deletion |
 NISCH
STAB1
NT5DC2
|
| nsv834697 | Chr.3:52366562 - 52545401 on Build GRCh38 | Loss |
SEMA3G
PHF7
NISCH
SMIM4
BAP1
STAB1
TNNC1
NT5DC2
PBRM1
DNAH1
|
| dgv8326n54 | Chr.3:52501570 - 52538040 on Build GRCh38 | Loss |
SMIM4
STAB1
NT5DC2
|
| nsv3820 | Chr.3:52496531 - 52530448 on Build GRCh38 | Insertion |
STAB1
NT5DC2
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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