UNC93B1 unc-93 homolog B1, TLR signaling regulator

Information
Symbol
UNC93B1
Type
protein-coding
Description
unc-93 homolog B1, TLR signaling regulator
Entrez Gene ID
81622
Genome
hg19
Position
chr11:67,758,571-67,771,567
Genome
hg38
Position
chr11:67,991,100-68,004,097
MIM
608204 OMIM
HGNC
HGNC:13481 HGNC
Ensembl
ENSG00000110057 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 8
Likely pathogenic 0 4
Benign 0 54
Likely benign 0 322
Conflicting classifications of pathogenicity 0 2
risk factor 0 2
Uncertain significance 0 374
Ranking
ClinVar
0
0
66
678
2
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 IIAE1
SYNONYM UNC93
SYNONYM UNC93B
SYNONYM Unc-93B1
MIM 608204 OMIM
HGNC HGNC:13481 HGNC
Ensembl ENSG00000110057 Ensembl
AllianceGenome HGNC:13481
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000227471.7 hg38 chr11 67,991,100 68,004,097 12,998
ENST00000227471.7 hg19 chr11 67,758,571 67,771,567 12,997
Genome browser