TSPYL2 TSPY like 2

Information
Symbol
TSPYL2
Type
protein-coding
Description
TSPY like 2
Entrez Gene ID
64061
Genome
hg19
Position
chrX:53,111,549-53,117,722
Genome
hg38
Position
chrX:53,082,367-53,088,540
MIM
300564 OMIM
HGNC
HGNC:24358 HGNC
Ensembl
ENSG00000184205 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 10
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 0 86
Ranking
ClinVar
0
0
0
98
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
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 CDA1
SYNONYM CINAP
SYNONYM CTCL
SYNONYM DENTT
SYNONYM HRIHFB2216
SYNONYM NP79
SYNONYM SE204
SYNONYM TSPX
MIM 300564 OMIM
HGNC HGNC:24358 HGNC
Ensembl ENSG00000184205 Ensembl
AllianceGenome HGNC:24358
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000375442.8 hg38 chrX 53,082,367 53,088,540 6,174
ENST00000375442.8 hg19 chrX 53,111,549 53,117,722 6,174
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