PLXNB3 plexin B3

Information
Symbol
PLXNB3
Type
protein-coding
Description
plexin B3
Entrez Gene ID
5365
Genome
hg19
Position
chrX:153,029,651-153,044,801
Genome
hg38
Position
chrX:153,764,196-153,779,346
MIM
300214 OMIM
HGNC
HGNC:9105 HGNC
Ensembl
ENSG00000198753 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 42
Likely benign 0 80
Conflicting classifications of pathogenicity 0 12
not provided 6 2
Uncertain significance 0 206
Ranking
ClinVar
0
0
0
326
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 PLEXB3
SYNONYM PLEXR
SYNONYM PLXN6
MIM 300214 OMIM
HGNC HGNC:9105 HGNC
Ensembl ENSG00000198753 Ensembl
AllianceGenome HGNC:9105
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000361971.10 hg38 chrX 153,764,249 153,779,341 15,093
ENST00000538966.5 hg38 chrX 153,764,196 153,779,346 15,151
ENST00000538966.5 hg19 chrX 153,029,651 153,044,801 15,151
ENST00000361971.10 hg19 chrX 153,029,704 153,044,796 15,093
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