UTP14C UTP14C small subunit processome component

Information
Symbol
UTP14C
Type
protein-coding
Description
UTP14C small subunit processome component
Entrez Gene ID
9724
Genome
hg19
Position
chr13:52,598,827-52,607,736
Genome
hg38
Position
chr13:52,024,691-52,033,600
MIM
608969 OMIM
HGNC
HGNC:20321 HGNC
Ensembl
ENSG00000253797 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 6
Benign 0 16
Likely benign 0 32
Conflicting classifications of pathogenicity 0 8
Uncertain significance 0 128
Ranking
ClinVar
0
0
22
156
6
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 2700066J21Rik
SYNONYM KIAA0266
SYNONYM UTP14B
MIM 608969 OMIM
HGNC HGNC:20321 HGNC
Ensembl ENSG00000253797 Ensembl
AllianceGenome HGNC:20321
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000521776.2 hg38 chr13 52,024,691 52,033,600 8,910
ENST00000521776.2 hg19 chr13 52,598,827 52,607,736 8,910
Genome browser