INMT-MINDY4 INMT-MINDY4 readthrough (NMD candidate)

Information
Symbol
INMT-MINDY4
Type
ncRNA
Description
INMT-MINDY4 readthrough (NMD candidate)
Entrez Gene ID
100526825
Genome
hg19
Position
chr7:30,791,753-30,931,696
Genome
hg38
Position
chr7:30,752,137-30,892,081
HGNC
HGNC:41995 HGNC
Ensembl
ENSG00000254959 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 14
Likely benign 0 14
Uncertain significance 0 158
Ranking
ClinVar
0
0
0
184
2
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
SYNONYM INMT-FAM188B
HGNC HGNC:41995 HGNC
Ensembl ENSG00000254959 Ensembl
AllianceGenome HGNC:41995
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000458257.5 hg38 chr7 30,752,137 30,892,081 139,945
ENST00000458257.5 hg19 chr7 30,791,753 30,931,696 139,944
Genome browser