ZC3H12C zinc finger CCCH-type containing 12C

Information
Symbol
ZC3H12C
Type
protein-coding
Description
zinc finger CCCH-type containing 12C
Entrez Gene ID
85463
Genome
hg19
Position
chr11:110,001,729-110,036,659
Genome
hg38
Position
chr11:110,131,004-110,165,934
MIM
615001 OMIM
HGNC
HGNC:29362 HGNC
Ensembl
ENSG00000149289 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 82
Ranking
ClinVar
0
0
0
86
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 MCPIP3
MIM 615001 OMIM
HGNC HGNC:29362 HGNC
Ensembl ENSG00000149289 Ensembl
AllianceGenome HGNC:29362
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000528673.5 hg38 chr11 110,131,004 110,165,934 34,931
ENST00000453089.2 hg38 chr11 110,135,854 110,171,839 35,986
ENST00000278590.8 hg38 chr11 110,093,392 110,171,841 78,450
ENST00000278590.8 hg19 chr11 109,964,118 110,042,566 78,449
ENST00000528673.5 hg19 chr11 110,001,729 110,036,659 34,931
ENST00000453089.2 hg19 chr11 110,006,579 110,042,564 35,986
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