Genomic Map
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Target Gene Details
Entrez Gene ID: | 1508 |
Gene Name: | cathepsin B |
Gene Aliases: |
APPS, CPSB |
Location: |
Chr.8:11842524-11868150 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CTSB | NM_001317237.1 | NP_001304166.1 | ||
| NM_001908.4 | NP_001899.1 | |||
| NM_147780.3 | NP_680090.1 | |||
| NM_147781.3 | NP_680091.1 | |||
| NM_147782.3 | NP_680092.1 | |||
| NM_147783.3 | NP_680093.1 | |||
| AA516096.1 | ||||
| AK097384.1 | ||||
| AK098296.1 | ||||
| BC095408.1 | AAH95408.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1034132 | Chr.8:11799524 - 12340733 on Build GRCh38 | Gain |
 FAM66D
FDFT1
USP17L7
CTSB
LOC392196
USP17L2
DEFB134
ZNF705D
LOC100133267
DEFB135
DEFB130
DEFB136
FAM86B1
FAM90A2P
|
| esv2762727 | Chr.8:11842150 - 11843744 on Build GRCh38 | Loss |
CTSB
|
| nsv516685 | Chr.8:11841238 - 12712690 on Build GRCh38 | Gain+Loss |
FAM66D
USP17L7
CTSB
LOC392196
USP17L2
DEFB134
FAM90A25P
ZNF705D
LOC100133267
DEFB109P1
DEFB135
DEFB130
DEFB136
FAM86B1
FAM86B2
LOC729732
LOC100506990
LOC649352
FAM90A2P
FAM66A
|
| esv34042 | Chr.8:11840828 - 11869308 on Build GRCh38 | Loss |
CTSB
|
| nsv1018042 | Chr.8:11809987 - 12024876 on Build GRCh38 | Gain |
DEFB135
DEFB136
FDFT1
CTSB
DEFB134
|
| esv3616259 | Chr.8:11841916 - 11843836 on Build GRCh38 | Loss |
CTSB
|
| nsv1032739 | Chr.8:11786294 - 11858964 on Build GRCh38 | Loss |
NEIL2
FDFT1
CTSB
|
| esv2668269 | Chr.8:11841914 - 11843834 on Build GRCh38 | Deletion |
CTSB
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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