The REEP1 gene homepage

General information
Gene symbol REEP1
Gene name receptor accessory protein 1
Chromosome 2
Chromosomal band p11.2
Imprinted Unknown
Genomic reference NG_013037.1
Transcript reference NM_022912.2
Exon/intron information NM_022912.2 exon/intron table
Associated with diseases HMN5B, SPG31
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 326
Unique public DNA variants reported 94
Individuals with public variants 510
Hidden variants 11
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
We gratefully acknowledge the role of Christian Beetz in curating this database (2016-2018).
Date created May 03, 2013
Date last updated February 26, 2024
Version REEP1:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_022912.2.
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
Homepage URL http://www.LOVD.nl/REEP1
HGNC 25786
Entrez Gene 65055
PubMed articles REEP1
OMIM - Gene 609139
OMIM - Diseases HMN5B (neuropathy, motor, distal, hereditary, type Vb (HMN-5B))
SPG31 (paraplegia, spastic, autosomal dominant, type 31 (SPG-31))
HGMD REEP1
GeneCards REEP1
GeneTests REEP1
Orphanet REEP1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00017606 2 transcript variant 2 NM_022912.2 NP_075063.1 326


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