SPATA32 spermatogenesis associated 32

Information
Symbol
SPATA32
Type
protein-coding
Description
spermatogenesis associated 32
Entrez Gene ID
124783
Genome
hg19
Position
chr17:43,331,760-43,339,461
Genome
hg38
Position
chr17:45,254,393-45,262,094
HGNC
HGNC:26349 HGNC
Ensembl
ENSG00000184361 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
42
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 :
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 AEP2
SYNONYM C17orf46
SYNONYM TEX34
SYNONYM VAD1.2
HGNC HGNC:26349 HGNC
Ensembl ENSG00000184361 Ensembl
AllianceGenome HGNC:26349
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000331780.5 hg38 chr17 45,254,393 45,262,094 7,702
ENST00000331780.5 hg19 chr17 43,331,760 43,339,461 7,702
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