SPATA2L spermatogenesis associated 2 like

Information
Symbol
SPATA2L
Type
protein-coding
Description
spermatogenesis associated 2 like
Entrez Gene ID
124044
Genome
hg19
Position
chr16:89,762,765-89,768,113
Genome
hg38
Position
chr16:89,696,357-89,701,705
HGNC
HGNC:28393 HGNC
Ensembl
ENSG00000158792 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 62
Ranking
ClinVar
0
0
0
66
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
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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 :
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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 :
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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 C16orf76
SYNONYM tamo
HGNC HGNC:28393 HGNC
Ensembl ENSG00000158792 Ensembl
AllianceGenome HGNC:28393
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000335360.11 hg38 chr16 89,696,357 89,701,705 5,349
ENST00000289805.10 hg38 chr16 89,696,357 89,701,705 5,349
ENST00000289805.10 hg19 chr16 89,762,765 89,768,113 5,349
ENST00000335360.11 hg19 chr16 89,762,765 89,768,113 5,349
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