SPAG7 sperm associated antigen 7

Information
Symbol
SPAG7
Type
protein-coding
Description
sperm associated antigen 7
Entrez Gene ID
9552
Genome
hg19
Position
chr17:4,862,521-4,871,112
Genome
hg38
Position
chr17:4,959,226-4,967,817
MIM
610056 OMIM
HGNC
HGNC:11216 HGNC
Ensembl
ENSG00000091640 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
28
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 :
Search word :
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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 ACRP
SYNONYM FSA-1
MIM 610056 OMIM
HGNC HGNC:11216 HGNC
Ensembl ENSG00000091640 Ensembl
AllianceGenome HGNC:11216
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000206020.8 hg38 chr17 4,959,226 4,967,817 8,592
ENST00000573366.5 hg38 chr17 4,959,256 4,967,191 7,936
ENST00000575142.5 hg38 chr17 4,959,226 4,967,790 8,565
ENST00000575142.5 hg19 chr17 4,862,521 4,871,085 8,565
ENST00000206020.8 hg19 chr17 4,862,521 4,871,112 8,592
ENST00000573366.5 hg19 chr17 4,862,551 4,870,486 7,936
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