IMP4 IMP U3 small nucleolar ribonucleoprotein 4

Information
Symbol
IMP4
Type
protein-coding
Description
IMP U3 small nucleolar ribonucleoprotein 4
Entrez Gene ID
92856
Genome
hg19
Position
chr2:131,100,470-131,105,540
Genome
hg38
Position
chr2:130,342,897-130,347,967
MIM
612981 OMIM
HGNC
HGNC:30856 HGNC
Ensembl
ENSG00000136718 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 1 0
Uncertain significance 0 46
Ranking
ClinVar
0
0
0
46
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 BXDC4
MIM 612981 OMIM
HGNC HGNC:30856 HGNC
Ensembl ENSG00000136718 Ensembl
AllianceGenome HGNC:30856
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000409935.5 hg38 chr2 130,342,877 130,346,519 3,643
ENST00000259239.8 hg38 chr2 130,342,897 130,347,967 5,071
ENST00000409935.5 hg19 chr2 131,100,450 131,104,092 3,643
ENST00000259239.8 hg19 chr2 131,100,470 131,105,540 5,071
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