SPATA9 spermatogenesis associated 9

Information
Symbol
SPATA9
Type
protein-coding
Description
spermatogenesis associated 9
Entrez Gene ID
83890
Genome
hg19
Position
chr5:94,994,019-95,018,695
Genome
hg38
Position
chr5:95,658,315-95,682,991
MIM
608039 OMIM
HGNC
HGNC:22988 HGNC
Ensembl
ENSG00000145757 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
36
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 NYD-SP16
MIM 608039 OMIM
HGNC HGNC:22988 HGNC
Ensembl ENSG00000145757 Ensembl
AllianceGenome HGNC:22988
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000274432.13 hg38 chr5 95,658,315 95,682,991 24,677
ENST00000274432.13 hg19 chr5 94,994,019 95,018,695 24,677
Genome browser