RNF32-DT RNF32 divergent transcript

Information
Symbol
RNF32-DT
Type
ncRNA
Description
RNF32 divergent transcript
Entrez Gene ID
100506380
Genome
hg19
Position
chr7:156,225,046-156,433,261
Genome
hg38
Position
chr7:156,432,352-156,640,567
MIM
610242 OMIM
HGNC
HGNC:48971 HGNC
Ensembl
ENSG00000182648 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 C7orf13
SYNONYM LINC01006
SYNONYM MY040
MIM 610242 OMIM
HGNC HGNC:48971 HGNC
Ensembl ENSG00000182648 Ensembl
AllianceGenome HGNC:48971
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000436670.2 hg38 chr7 156,436,980 156,445,588 8,609
ENST00000663891.1 hg38 chr7 156,479,683 156,640,520 160,838
ENST00000660473.1 hg38 chr7 156,472,116 156,640,535 168,420
ENST00000671433.1 hg38 chr7 156,472,127 156,639,057 166,931
ENST00000458645.5 hg38 chr7 156,584,160 156,640,592 56,433
ENST00000656505.1 hg38 chr7 156,471,126 156,640,296 169,171
ENST00000652322.1 hg38 chr7 156,432,352 156,640,567 208,216
ENST00000652322.1 hg19 chr7 156,225,046 156,433,261 208,216
ENST00000436670.2 hg19 chr7 156,229,674 156,238,282 8,609
ENST00000458645.5 hg19 chr7 156,376,854 156,433,286 56,433
ENST00000656505.1 hg19 chr7 156,263,820 156,432,990 169,171
ENST00000660473.1 hg19 chr7 156,264,810 156,433,229 168,420
ENST00000671433.1 hg19 chr7 156,264,821 156,431,751 166,931
ENST00000663891.1 hg19 chr7 156,272,377 156,433,214 160,838
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