PLXNC1 plexin C1

Information
Symbol
PLXNC1
Type
protein-coding
Description
plexin C1
Entrez Gene ID
10154
Genome
hg19
Position
chr12:94,542,353-94,701,451
Genome
hg38
Position
chr12:94,148,577-94,307,675
MIM
604259 OMIM
HGNC
HGNC:9106 HGNC
Ensembl
ENSG00000136040 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 16
Likely benign 0 34
Uncertain significance 0 142
Ranking
ClinVar
0
0
4
186
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 :
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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 CD232
SYNONYM PLXN-C1
SYNONYM VESPR
MIM 604259 OMIM
HGNC HGNC:9106 HGNC
Ensembl ENSG00000136040 Ensembl
AllianceGenome HGNC:9106
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000545312.1 hg38 chr12 94,262,521 94,305,598 43,078
ENST00000258526.9 hg38 chr12 94,148,577 94,307,675 159,099
ENST00000547057.5 hg38 chr12 94,254,528 94,305,655 51,128
ENST00000258526.9 hg19 chr12 94,542,353 94,701,451 159,099
ENST00000547057.5 hg19 chr12 94,648,304 94,699,431 51,128
ENST00000545312.1 hg19 chr12 94,656,297 94,699,374 43,078
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