HNRNPM heterogeneous nuclear ribonucleoprotein M

Information
Symbol
HNRNPM
Type
protein-coding
Description
heterogeneous nuclear ribonucleoprotein M
Entrez Gene ID
4670
Genome
hg19
Position
chr19:8,509,859-8,553,998
Genome
hg38
Position
chr19:8,444,975-8,489,114
MIM
160994 OMIM
HGNC
HGNC:5046 HGNC
Ensembl
ENSG00000099783 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 4
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
72
4
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 :
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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 CEAR
SYNONYM HNRNPM4
SYNONYM HNRPM
SYNONYM HNRPM4
SYNONYM HTGR1
SYNONYM NAGR1
SYNONYM hnRNP M
MIM 160994 OMIM
HGNC HGNC:5046 HGNC
Ensembl ENSG00000099783 Ensembl
AllianceGenome HGNC:5046
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000325495.9 hg38 chr19 8,444,975 8,489,114 44,140
ENST00000348943.7 hg38 chr19 8,444,767 8,489,114 44,348
ENST00000348943.7 hg19 chr19 8,509,651 8,553,998 44,348
ENST00000325495.9 hg19 chr19 8,509,859 8,553,998 44,140
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