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: | Within Exon 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CTSB | NM_001317237.1 | 7 | 704 | NP_001304166.1 |
| NM_001908.4 | 7 | 735 | NP_001899.1 | |
| NM_147780.3 | 9 | 897 | NP_680090.1 | |
| NM_147781.3 | 8 | 854 | NP_680091.1 | |
| NM_147782.3 | 8 | 823 | NP_680092.1 | |
| NM_147783.3 | 8 | 809 | NP_680093.1 | |
| XM_006716244.2 | 9 | 921 | XP_006716307.1 | |
| XM_006716245.2 | 7 | 1025 | XP_006716308.1 | |
| XM_011543812.2 | 9 | 830 | XP_011542114.1 | |
| XM_017013097.1 | 8 | 811 | XP_016868586.1 | |
| XM_017013098.1 | 8 | 811 | XP_016868587.1 | |
| XM_017013099.1 | 9 | 853 | XP_016868588.1 | |
| XM_017013100.1 | 8 | 755 | XP_016868589.1 | |
| XM_017013101.1 | 4 | 278 | XP_016868590.1 | |
| AK075393.1 | 7 | 711 | ||
| AK092070.1 | 8 | 746 | ||
| AK097384.1 | 2 | 665 | ||
| AK130184.1 | 7 | 672 | ||
| AK290239.1 | 7 | 672 | ||
| AK296845.1 | ||||
| AK297687.1 | 5 | 436 | ||
| AL543654.3 | 8 | 783 | ||
| BC010240.1 | 8 | 752 | AAH10240.1 | |
| BC095408.1 | 7 | 672 | AAH95408.1 | |
| BM008741.1 | ||||
| BX647765.1 | 7 | 595 | CAI46053.1 | |
| BX647952.1 | 7 | 675 | ||
| BX648239.1 | 4 | 4746 | ||
| L16510.1 | 8 | 737 | AAC37547.1 | |
| M13230.1 | 3 | 170 | AAA52125.1 | |
| M14221.1 | 8 | 754 | AAA52129.1 | |
| Y18460.1 | 3 | 242 | CAA77178.1 |
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 |
 ZNF705D
DEFB136
DEFB130
DEFB134
LOC100133267
FDFT1
USP17L2
DEFB135
USP17L7
FAM66D
FAM90A2P
CTSB
LOC392196
FAM86B1
|
| nsv610293 | Chr.8:11841238 - 12072225 on Build GRCh38 | Gain |
DEFB136
DEFB134
CTSB
LOC100133267
DEFB135
|
| esv34042 | Chr.8:11840828 - 11869308 on Build GRCh38 | Loss |
CTSB
|
| nsv1018042 | Chr.8:11809987 - 12024876 on Build GRCh38 | Gain |
DEFB136
DEFB134
CTSB
FDFT1
DEFB135
|
| esv3572516 | Chr.8:11844191 - 11853761 on Build GRCh38 | Loss |
CTSB
|
| nsv1032739 | Chr.8:11786294 - 11858964 on Build GRCh38 | Loss |
CTSB
FDFT1
NEIL2
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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