NMU neuromedin U

Information
Symbol
NMU
Type
protein-coding
Description
neuromedin U
Entrez Gene ID
10874
Genome
hg19
Position
chr4:56,461,398-56,502,465
Genome
hg38
Position
chr4:55,595,231-55,636,298
MIM
605103 OMIM
HGNC
HGNC:7859 HGNC
Ensembl
ENSG00000109255 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
22
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
MIM 605103 OMIM
HGNC HGNC:7859 HGNC
Ensembl ENSG00000109255 Ensembl
AllianceGenome HGNC:7859
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000511469.5 hg38 chr4 55,595,229 55,636,284 41,056
ENST00000264218.7 hg38 chr4 55,595,231 55,636,298 41,068
ENST00000505262.5 hg38 chr4 55,595,234 55,636,259 41,026
ENST00000507338.1 hg38 chr4 55,595,284 55,636,268 40,985
ENST00000511469.5 hg19 chr4 56,461,396 56,502,451 41,056
ENST00000264218.7 hg19 chr4 56,461,398 56,502,465 41,068
ENST00000505262.5 hg19 chr4 56,461,401 56,502,426 41,026
ENST00000507338.1 hg19 chr4 56,461,451 56,502,435 40,985
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