PCLAF PCNA clamp associated factor

Information
Symbol
PCLAF
Type
protein-coding
Description
PCNA clamp associated factor
Entrez Gene ID
9768
Genome
hg19
Position
chr15:64,656,503-64,673,640
Genome
hg38
Position
chr15:64,364,304-64,381,441
MIM
610696 OMIM
HGNC
HGNC:28961 HGNC
Ensembl
ENSG00000166803 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
12
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 KIAA0101
SYNONYM L5
SYNONYM NS5ATP9
SYNONYM OEATC
SYNONYM OEATC-1
SYNONYM OEATC1
SYNONYM PAF
SYNONYM PAF15
SYNONYM p15(PAF)
SYNONYM p15/PAF
SYNONYM p15PAF
MIM 610696 OMIM
HGNC HGNC:28961 HGNC
Ensembl ENSG00000166803 Ensembl
AllianceGenome HGNC:28961
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000380258.6 hg38 chr15 64,365,365 64,381,444 16,080
ENST00000558008.3 hg38 chr15 64,365,734 64,381,438 15,705
ENST00000300035.9 hg38 chr15 64,364,304 64,381,441 17,138
ENST00000559519.5 hg38 chr15 64,365,606 64,381,441 15,836
ENST00000300035.9 hg19 chr15 64,656,503 64,673,640 17,138
ENST00000380258.6 hg19 chr15 64,657,564 64,673,643 16,080
ENST00000559519.5 hg19 chr15 64,657,805 64,673,640 15,836
ENST00000558008.3 hg19 chr15 64,657,933 64,673,637 15,705
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