PSMD7-DT PSMD7 divergent transcript

Information
Symbol
PSMD7-DT
Type
ncRNA
Description
PSMD7 divergent transcript
Entrez Gene ID
101928035
Genome
hg19
Position
chr16:74,195,178-74,330,396
Genome
hg38
Position
chr16:74,161,279-74,296,498
HGNC
HGNC:53056 HGNC
Ensembl
ENSG00000261404 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
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
[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
HGNC HGNC:53056 HGNC
Ensembl ENSG00000261404 Ensembl
AllianceGenome HGNC:53056
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000641127.1 hg38 chr16 73,943,078 74,206,165 263,088
ENST00000641872.1 hg38 chr16 73,948,811 74,181,935 233,125
ENST00000641894.1 hg38 chr16 73,996,801 74,019,971 23,171
ENST00000641560.1 hg38 chr16 74,103,086 74,296,756 193,671
ENST00000650425.1 hg38 chr16 74,161,279 74,296,498 135,220
ENST00000641127.1 hg19 chr16 73,976,977 74,240,064 263,088
ENST00000641872.1 hg19 chr16 73,982,710 74,215,834 233,125
ENST00000641894.1 hg19 chr16 74,030,700 74,053,870 23,171
ENST00000641560.1 hg19 chr16 74,136,985 74,330,654 193,670
ENST00000650425.1 hg19 chr16 74,195,178 74,330,396 135,219
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