Genomic Map
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Target Gene Details
Entrez Gene ID: | 1512 |
Gene Name: | cathepsin H |
Gene Aliases: |
ACC-4, ACC-5, ACC4, ACC5, CPSB |
Location: |
Chr.15:78921750-78945098 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CTSH | NM_001319137.1 | NP_001306066.1 | ||
| NM_004390.4 | NP_004381.2 | |||
| XM_005254181.2 | XP_005254238.1 | |||
| XM_011521276.1 | XP_011519578.1 | |||
| XM_017021951.1 | XP_016877440.1 | |||
| XM_017021952.1 | XP_016877441.1 | |||
| AF426247.1 | AAL23961.1 | |||
| AF426248.1 | AAL23962.1 | |||
| AK130158.1 | ||||
| AK295583.1 | ||||
| AK309491.1 | ||||
| AK314698.1 | ||||
| AL110099.1 | ||||
| BC002479.2 | AAH02479.1 | |||
| BG775606.1 | ||||
| BM849425.1 | ||||
| CR456881.1 | CAG33162.1 | |||
| X07549.1 | CAA30428.1 | |||
| X16832.1 | CAA34734.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3636994 | Chr.15:78934166 - 78940717 on Build GRCh38 | Loss |
 CTSH
|
| esv3552725 | Chr.15:78928018 - 78941559 on Build GRCh38 | Deletion |
CTSH
|
| nsv1629 | Chr.15:78910014 - 78940030 on Build GRCh38 | Insertion |
CTSH
|
| esv33573 | Chr.15:78761142 - 79001539 on Build GRCh38 | Gain+Loss |
ADAMTS7
MORF4L1
CTSH
RASGRF1
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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