C2CD4D C2 calcium dependent domain containing 4D

Information
Symbol
C2CD4D
Type
protein-coding
Description
C2 calcium dependent domain containing 4D
Entrez Gene ID
100191040
Genome
hg19
Position
chr1:151,810,295-151,813,033
Genome
hg38
Position
chr1:151,837,819-151,840,557
HGNC
HGNC:37210 HGNC
Ensembl
ENSG00000225556 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 50
Ranking
ClinVar
0
0
0
50
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 :
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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 FAM148D
HGNC HGNC:37210 HGNC
Ensembl ENSG00000225556 Ensembl
AllianceGenome HGNC:37210
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000454109.1 hg38 chr1 151,837,819 151,840,557 2,739
ENST00000694869.1 hg38 chr1 151,837,821 151,840,164 2,344
ENST00000694868.1 hg38 chr1 151,837,818 151,839,820 2,003
ENST00000694868.1 hg19 chr1 151,810,294 151,812,296 2,003
ENST00000454109.1 hg19 chr1 151,810,295 151,813,033 2,739
ENST00000694869.1 hg19 chr1 151,810,297 151,812,640 2,344
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