C1QTNF6 C1q and TNF related 6

Information
Symbol
C1QTNF6
Type
protein-coding
Description
C1q and TNF related 6
Entrez Gene ID
114904
Genome
hg19
Position
chr22:37,576,206-37,584,287
Genome
hg38
Position
chr22:37,180,166-37,188,247
MIM
614910 OMIM
HGNC
HGNC:14343 HGNC
Ensembl
ENSG00000133466 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 2
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
44
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
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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 :
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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 CTFP6
SYNONYM CTRP6
SYNONYM ZACRP6
MIM 614910 OMIM
HGNC HGNC:14343 HGNC
Ensembl ENSG00000133466 Ensembl
AllianceGenome HGNC:14343
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000397110.6 hg38 chr22 37,180,167 37,188,286 8,120
ENST00000434784.1 hg38 chr22 37,182,174 37,188,236 6,063
ENST00000337843.7 hg38 chr22 37,180,166 37,188,247 8,082
ENST00000337843.7 hg19 chr22 37,576,206 37,584,287 8,082
ENST00000397110.6 hg19 chr22 37,576,207 37,584,326 8,120
ENST00000434784.1 hg19 chr22 37,578,214 37,584,276 6,063
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