RAMP2 receptor activity modifying protein 2

Information
Symbol
RAMP2
Type
protein-coding
Description
receptor activity modifying protein 2
Entrez Gene ID
10266
Genome
hg19
Position
chr17:40,913,245-40,915,059
Genome
hg38
Position
chr17:42,761,227-42,763,041
MIM
605154 OMIM
HGNC
HGNC:9844 HGNC
Ensembl
ENSG00000131477 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
24
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
MIM 605154 OMIM
HGNC HGNC:9844 HGNC
Ensembl ENSG00000131477 Ensembl
AllianceGenome HGNC:9844
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000253796.10 hg38 chr17 42,761,227 42,763,041 1,815
ENST00000588576.1 hg38 chr17 42,761,258 42,763,002 1,745
ENST00000587142.5 hg38 chr17 42,761,258 42,762,854 1,597
ENST00000589683.5 hg38 chr17 42,760,775 42,763,041 2,267
ENST00000589683.5 hg19 chr17 40,912,793 40,915,059 2,267
ENST00000253796.10 hg19 chr17 40,913,245 40,915,059 1,815
ENST00000587142.5 hg19 chr17 40,913,276 40,914,872 1,597
ENST00000588576.1 hg19 chr17 40,913,276 40,915,020 1,745
Genome browser