CSAG2 CSAG family member 2

Information
Symbol
CSAG2
Type
protein-coding
Description
CSAG family member 2
Entrez Gene ID
102723547
Genome
hg38
Position
chrX:152,708,261-152,709,273
MIM
301096 OMIM
HGNC
HGNC:16847 HGNC
Ensembl
ENSG00000268902 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Ranking
ClinVar
0
0
0
0
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
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 CSAG3B
SYNONYM CT24.2
SYNONYM TRAG-3
SYNONYM TRAG3
MIM 301096 OMIM
HGNC HGNC:16847 HGNC
Ensembl ENSG00000268902 Ensembl
AllianceGenome HGNC:16847
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000638741.2 hg38 chrX 152,708,261 152,709,273 1,013
ENST00000640702.1 hg38 chrX 152,708,264 152,709,265 1,002
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