DENND2B DENN domain containing 2B

Information
Symbol
DENND2B
Type
protein-coding
Description
DENN domain containing 2B
Entrez Gene ID
6764
Genome
hg19
Position
chr11:8,714,898-8,932,498
Genome
hg38
Position
chr11:8,693,351-8,910,951
MIM
140750 OMIM
HGNC
HGNC:11350 HGNC
Ensembl
ENSG00000166444 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 14
Likely benign 0 14
not provided 1 0
Uncertain significance 0 140
Ranking
ClinVar
0
0
4
162
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
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 HTS1
SYNONYM ST5
SYNONYM p126
MIM 140750 OMIM
HGNC HGNC:11350 HGNC
Ensembl ENSG00000166444 Ensembl
AllianceGenome HGNC:11350
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000526757.5 hg38 chr11 8,693,351 8,811,341 117,991
ENST00000626808.2 hg38 chr11 8,711,968 8,766,701 54,734
ENST00000313726.11 hg38 chr11 8,693,352 8,810,674 117,323
ENST00000530438.5 hg38 chr11 8,694,096 8,811,016 116,921
ENST00000534278.5 hg38 chr11 8,693,899 8,708,081 14,183
ENST00000526099.5 hg38 chr11 8,693,748 8,718,477 24,730
ENST00000530991.5 hg38 chr11 8,693,353 8,719,143 25,791
ENST00000534127.5 hg38 chr11 8,693,351 8,910,951 217,601
ENST00000313726.11 hg19 chr11 8,714,899 8,832,221 117,323
ENST00000526099.5 hg19 chr11 8,715,295 8,740,024 24,730
ENST00000526757.5 hg19 chr11 8,714,898 8,832,888 117,991
ENST00000530991.5 hg19 chr11 8,714,900 8,740,690 25,791
ENST00000530438.5 hg19 chr11 8,715,643 8,832,563 116,921
ENST00000534127.5 hg19 chr11 8,714,898 8,932,498 217,601
ENST00000534278.5 hg19 chr11 8,715,446 8,729,628 14,183
ENST00000626808.2 hg19 chr11 8,733,515 8,788,248 54,734
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