CXXC5 CXXC finger protein 5

Information
Symbol
CXXC5
Type
protein-coding
Description
CXXC finger protein 5
Entrez Gene ID
51523
Genome
hg19
Position
chr5:139,027,934-139,063,467
Genome
hg38
Position
chr5:139,648,349-139,683,882
MIM
612752 OMIM
HGNC
HGNC:26943 HGNC
Ensembl
ENSG00000171604 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
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 :
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 CF5
SYNONYM HSPC195
SYNONYM RINF
SYNONYM WID
MIM 612752 OMIM
HGNC HGNC:26943 HGNC
Ensembl ENSG00000171604 Ensembl
AllianceGenome HGNC:26943
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000302517.8 hg38 chr5 139,648,349 139,683,882 35,534
ENST00000511048.1 hg38 chr5 139,648,933 139,683,593 34,661
ENST00000302517.8 hg19 chr5 139,027,934 139,063,467 35,534
ENST00000511048.1 hg19 chr5 139,028,518 139,063,178 34,661
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