GPRIN3 GPRIN family member 3

Information
Symbol
GPRIN3
Type
protein-coding
Description
GPRIN family member 3
Entrez Gene ID
285513
Genome
hg19
Position
chr4:90,157,534-90,229,088
Genome
hg38
Position
chr4:89,236,383-89,307,937
MIM
611241 OMIM
HGNC
HGNC:27733 HGNC
Ensembl
ENSG00000185477 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 90
Ranking
ClinVar
0
0
0
98
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM GRIN3
MIM 611241 OMIM
HGNC HGNC:27733 HGNC
Ensembl ENSG00000185477 Ensembl
AllianceGenome HGNC:27733
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000715382.1 hg38 chr4 89,236,383 89,307,937 71,555
ENST00000609438.2 hg38 chr4 89,236,383 89,307,800 71,418
ENST00000333209.4 hg38 chr4 89,244,935 89,251,194 6,260
ENST00000609438.2 hg19 chr4 90,157,534 90,228,951 71,418
ENST00000715382.1 hg19 chr4 90,157,534 90,229,088 71,555
ENST00000333209.4 hg19 chr4 90,166,086 90,172,345 6,260
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