Genomic Map
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Target Gene Details
Entrez Gene ID: | 5654 |
Gene Name: | HtrA serine peptidase 1 |
Gene Aliases: |
ARMD7, CADASIL2, CARASIL, HtrA, L56, ORF480, PRSS11 |
Location: |
Chr.10:122461525-122514908 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HTRA1 | NM_002775.4 | NP_002766.1 | ||
| AF097709.1 | AAC97211.1 | |||
| AK091944.1 | ||||
| AK092476.1 | ||||
| AK290089.1 | ||||
| BC011352.1 | ||||
| D87258.1 | BAA13322.1 | |||
| DA633502.1 | ||||
| Y07921.1 | CAA69226.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv7580 | Chr.10:122446276 - 122490980 on Build GRCh38 | Deletion |
 HTRA1
ARMS2
|
| nsv825594 | Chr.10:122434264 - 122505709 on Build GRCh38 | Gain |
HTRA1
ARMS2
|
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Additional Information:
For this assay, SNP(s) [rs77802229] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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