The GPR56 gene homepage

General information
Gene symbol GPR56
Gene name G protein-coupled receptor 56
Chromosome 16
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_011643.1
Transcript reference NM_001145770.1, NM_001145771.1, NM_001145772.1, NM_001145773.1, NM_001145774.1, NM_005682.5, NM_201524.2, NM_201525.2, XM_005256237.1, XM_005256238.1, XM_005256240.2, XM_005256242.2, XM_005256245.1, XM_005256247.1, XM_005256249.1, XM_005256251.2, XM_005256254.1, XM_005256255.1
Associated with diseases ID, Polymicrogyria, bilateral frontoparietal, polymicrogyria, bilateral perisylvian, autosomal recessive
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 208
Unique public DNA variants reported 23
Individuals with public variants 35
Hidden variants 193
Date created November 30, -0001
Date last updated September 28, 2016
Version GPR56:160928

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
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:4512
OMIM - Gene 604110
OMIM - Diseases Polymicrogyria, bilateral frontoparietal
polymicrogyria, bilateral perisylvian, autosomal recessive


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00011870 16 transcript variant 1 NM_005682.5 NP_005673.3 208
00011871 16 transcript variant 5 NM_001145770.1 NP_001139242.1 208
00011872 16 transcript variant 6 NM_001145772.1 NP_001139244.1 208
00011873 16 transcript variant 2 NM_201524.2 NP_958932.1 208
00011874 16 transcript variant 4 NM_001145771.1 NP_001139243.1 208
00011875 16 transcript variant 8 NM_001145773.1 NP_001139245.1 208
00011876 16 transcript variant 3 NM_201525.2 NP_958933.1 208
00011877 16 transcript variant 7 NM_001145774.1 NP_001139246.1 208
00037813 16 transcript variant X2 XM_005256238.1 XP_005256295.1 -
00037814 16 transcript variant X13 XM_005256249.1 XP_005256306.1 -
00037815 16 transcript variant X1 XM_005256237.1 XP_005256294.1 -
00037816 16 transcript variant X11 XM_005256247.1 XP_005256304.1 -
00037817 16 transcript variant X18 XM_005256254.1 XP_005256311.1 -
00037818 16 transcript variant X6 XM_005256242.2 XP_005256299.1 -
00037819 16 transcript variant X15 XM_005256251.2 XP_005256308.1 -
00037820 16 transcript variant X19 XM_005256255.1 XP_005256312.1 -
00037821 16 transcript variant X9 XM_005256245.1 XP_005256302.1 -
00037822 16 transcript variant X4 XM_005256240.2 XP_005256297.1 -