NOC4L nucleolar complex associated 4 homolog

Information
Symbol
NOC4L
Type
protein-coding
Description
nucleolar complex associated 4 homolog
Entrez Gene ID
79050
Genome
hg19
Position
chr12:132,629,002-132,637,013
Genome
hg38
Position
chr12:132,144,457-132,152,468
MIM
612819 OMIM
HGNC
HGNC:28461 HGNC
Ensembl
ENSG00000184967 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 116
Ranking
ClinVar
0
0
0
124
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
SYNONYM NET49
SYNONYM NOC4
SYNONYM UTP19
MIM 612819 OMIM
HGNC HGNC:28461 HGNC
Ensembl ENSG00000184967 Ensembl
AllianceGenome HGNC:28461
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000330579.6 hg38 chr12 132,144,457 132,152,468 8,012
ENST00000330579.6 hg19 chr12 132,629,002 132,637,013 8,012
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