C1QTNF9B C1q and TNF related 9B

Information
Symbol
C1QTNF9B
Type
protein-coding
Description
C1q and TNF related 9B
Entrez Gene ID
387911
Genome
hg19
Position
chr13:24,465,238-24,471,641
Genome
hg38
Position
chr13:23,891,099-23,897,502
MIM
614148 OMIM
HGNC
HGNC:34072 HGNC
Ensembl
ENSG00000205863 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 8
not provided 2 0
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
54
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 :
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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 CTRP9B
MIM 614148 OMIM
HGNC HGNC:34072 HGNC
Ensembl ENSG00000205863 Ensembl
AllianceGenome HGNC:34072
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000382137.8 hg38 chr13 23,891,099 23,897,055 5,957
ENST00000713589.1 hg38 chr13 23,891,099 23,897,502 6,404
ENST00000382145.5 hg38 chr13 23,891,099 23,897,502 6,404
ENST00000382137.8 hg19 chr13 24,465,238 24,471,194 5,957
ENST00000382145.5 hg19 chr13 24,465,238 24,471,641 6,404
ENST00000713589.1 hg19 chr13 24,465,238 24,471,641 6,404
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