The HTRA1 gene homepage

General information
Gene symbol HTRA1
Gene name HtrA serine peptidase 1
Chromosome 10
Chromosomal band q26.3
Imprinted Unknown
Genomic reference NG_011554.1
Transcript reference NM_002775.4
Associated with diseases ARMD-7, Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 27
Unique public DNA variants reported 23
Individuals with public variants 2
Hidden variants 15
Date created May 03, 2013
Date last updated February 08, 2021
Version HTRA1:210208

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 9476
Entrez Gene 5654
PubMed articles HTRA1
OMIM - Gene 602194
OMIM - Diseases ARMD-7 (macular degeneration, age-related, type 7 (ARMD-7))
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
Orphanet HTRA1

Active transcripts




NCBI ID     

NCBI Protein ID     

00009733 10 HtrA serine peptidase 1 NM_002775.4 NP_002766.1 27

Copyright & disclaimer
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