COMMD9 COMM domain containing 9

Information
Symbol
COMMD9
Type
protein-coding
Description
COMM domain containing 9
Entrez Gene ID
29099
Genome
hg19
Position
chr11:36,293,842-36,310,974
Genome
hg38
Position
chr11:36,272,292-36,289,424
MIM
612299 OMIM
HGNC
HGNC:25014 HGNC
Ensembl
ENSG00000110442 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
not provided 1 0
Uncertain significance 0 20
Ranking
ClinVar
0
0
0
24
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 C11orf55
SYNONYM HSPC166
SYNONYM LINC00610
MIM 612299 OMIM
HGNC HGNC:25014 HGNC
Ensembl ENSG00000110442 Ensembl
AllianceGenome HGNC:25014
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000532705.1 hg38 chr11 36,274,325 36,289,424 15,100
ENST00000263401.10 hg38 chr11 36,272,292 36,289,424 17,133
ENST00000452374.6 hg38 chr11 36,274,223 36,289,449 15,227
ENST00000263401.10 hg19 chr11 36,293,842 36,310,974 17,133
ENST00000452374.6 hg19 chr11 36,295,773 36,310,999 15,227
ENST00000532705.1 hg19 chr11 36,295,875 36,310,974 15,100
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