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When using or discussing LOVD please refer to:
Fokkema IFAC, Den Dunnen JT and Taschner PEM (2005). LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-Box" approach.
Hum Mutat. 2005 Aug;26(2):63-8.

LDLRAP1 @ www.ucl.ac.uk/ldlr/LOVDv.1.1.0/
General information
Gene name: LOW DENSITY LIPOPROTEIN RECEPTOR ADAPTOR PROTEIN 1
Gene symbol: LDLRAP1
Chromosome Location: 1p36-35
Database location: www.ucl.ac.uk/ldlr/LOVDv.1.1.0/
Curator: Sarah Leigh
Date of creation: February 12, 2010
Last update: November 22, 2010
Version: LDLRAP1 101122
Add allelic variant: Submit an allelic variant
First time submitters: Register here
Genomic reference sequence: LDLRAP1 reference sequence for describing allelic variants
Total number of allelic variants: 39
Number of unique allelic variants: 32
NOTE: We have used all reasonable efforts to ensure that the information displayed on these pages and contained in the databases is of high quality. We make no warranty, express or implied, as to its accuracy or that the information is fit for a particular purpose, and will not be held responsible for any consequences arising out of any inaccuracies or omissions. Individuals, organisations and companies which use this database do so on the understanding that no liability whatsoever either direct or indirect shall rest upon University College London or any of it's employees or agents for the effects of any product, process or method that may be produced or adopted by any part, notwithstanding that the formulation of such product, process or method may be based upon information here provided. If you find any errors or omissions, please contact the curator and every effort will be made to rectify the situation.

Allelic variant tables
Complete allelic variant table: Listing of all allelic variants in the LDLRAP1 database
Summary tables: Summary of all allelic variants in the LDLRAP1 database, sorted by type of variant (with graphical displays and statistics)
Polymorphism table: Listing of all LDLRAP1 variants reported to have no noticeable phenotypic effect

Search the database
By type of variant: View allelic variant table after selecting one type of variant
Simple search: Query the database by selecting the most important variables (exon number, type of variant, disease phenotype)
Advanced search: Query the database by selecting a combination of variables

Links to other resources:
Entrez Gene (LocusLink) 26119
OMIM - gene 605747
OMIM - disease 603813 (ARH)
HGMD LDLRAP1

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