PLAC4 placenta enriched 4

Information
Symbol
PLAC4
Type
ncRNA
Description
placenta enriched 4
Entrez Gene ID
191585
Genome
hg19
Position
chr21:42,548,249-42,558,700
Genome
hg38
Position
chr21:41,176,322-41,186,773
MIM
613770 OMIM
HGNC
HGNC:14616 HGNC
Ensembl
ENSG00000280109 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Ranking
ClinVar
0
0
0
0
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
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 C21orf115
SYNONYM PRED78
MIM 613770 OMIM
HGNC HGNC:14616 HGNC
Ensembl ENSG00000280109 Ensembl
AllianceGenome HGNC:14616
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000645185.1 hg38 chr21 41,175,231 41,185,239 10,009
ENST00000440221.2 hg38 chr21 41,176,446 41,186,788 10,343
ENST00000430327.6 hg38 chr21 41,176,322 41,186,773 10,452
ENST00000414699.1 hg38 chr21 41,180,532 41,186,320 5,789
ENST00000645185.1 hg19 chr21 42,547,158 42,557,166 10,009
ENST00000430327.6 hg19 chr21 42,548,249 42,558,700 10,452
ENST00000440221.2 hg19 chr21 42,548,373 42,558,715 10,343
ENST00000414699.1 hg19 chr21 42,552,459 42,558,247 5,789
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