CELF6 CUGBP Elav-like family member 6

Information
Symbol
CELF6
Type
protein-coding
Description
CUGBP Elav-like family member 6
Entrez Gene ID
60677
Genome
hg19
Position
chr15:72,577,068-72,612,498
Genome
hg38
Position
chr15:72,284,727-72,320,157
MIM
612681 OMIM
HGNC
HGNC:14059 HGNC
Ensembl
ENSG00000140488 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 4
Uncertain significance 0 32
Ranking
ClinVar
0
0
2
42
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
Category :
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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 BRUNOL6
MIM 612681 OMIM
HGNC HGNC:14059 HGNC
Ensembl ENSG00000140488 Ensembl
AllianceGenome HGNC:14059
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000567083.2 hg38 chr15 72,286,248 72,319,882 33,635
ENST00000395258.7 hg38 chr15 72,285,951 72,306,292 20,342
ENST00000287202.10 hg38 chr15 72,284,727 72,320,157 35,431
ENST00000543764.6 hg38 chr15 72,285,905 72,306,315 20,411
ENST00000287202.10 hg19 chr15 72,577,068 72,612,498 35,431
ENST00000543764.6 hg19 chr15 72,578,246 72,598,656 20,411
ENST00000395258.7 hg19 chr15 72,578,292 72,598,633 20,342
ENST00000567083.2 hg19 chr15 72,578,589 72,612,223 33,635
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