PXN paxillin

Information
Symbol
PXN
Type
protein-coding
Description
paxillin
Entrez Gene ID
5829
Genome
hg19
Position
chr12:120,648,250-120,703,533
Genome
hg38
Position
chr12:120,210,447-120,265,730
MIM
602505 OMIM
HGNC
HGNC:9718 HGNC
Ensembl
ENSG00000089159 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 6
Uncertain significance 0 86
Ranking
ClinVar
0
0
0
102
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 602505 OMIM
HGNC HGNC:9718 HGNC
Ensembl ENSG00000089159 Ensembl
AllianceGenome HGNC:9718
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000637617.2 hg38 chr12 120,210,447 120,265,730 55,284
ENST00000458477.6 hg38 chr12 120,210,447 120,250,161 39,715
ENST00000267257.11 hg38 chr12 120,210,439 120,265,771 55,333
ENST00000228307.11 hg38 chr12 120,210,447 120,265,771 55,325
ENST00000536957.5 hg38 chr12 120,210,448 120,226,844 16,397
ENST00000424649.6 hg38 chr12 120,210,447 120,265,771 55,325
ENST00000267257.11 hg19 chr12 120,648,242 120,703,574 55,333
ENST00000458477.6 hg19 chr12 120,648,250 120,687,964 39,715
ENST00000228307.11 hg19 chr12 120,648,250 120,703,574 55,325
ENST00000424649.6 hg19 chr12 120,648,250 120,703,574 55,325
ENST00000536957.5 hg19 chr12 120,648,251 120,664,647 16,397
ENST00000637617.2 hg19 chr12 120,648,250 120,703,533 55,284
Genome browser