C2CD2L C2CD2 like

Information
Symbol
C2CD2L
Type
protein-coding
Description
C2CD2 like
Entrez Gene ID
9854
Genome
hg19
Position
chr11:118,978,093-118,989,254
Genome
hg38
Position
chr11:119,107,383-119,118,544
MIM
617582 OMIM
HGNC
HGNC:29000 HGNC
Ensembl
ENSG00000172375 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 86
Ranking
ClinVar
0
0
0
94
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 DLNB23
SYNONYM TMEM24
MIM 617582 OMIM
HGNC HGNC:29000 HGNC
Ensembl ENSG00000172375 Ensembl
AllianceGenome HGNC:29000
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000336702.7 hg38 chr11 119,107,383 119,118,544 11,162
ENST00000648610.2 hg38 chr11 119,107,344 119,118,544 11,201
ENST00000648610.2 hg19 chr11 118,978,054 118,989,254 11,201
ENST00000336702.7 hg19 chr11 118,978,093 118,989,254 11,162
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