SPATA18 spermatogenesis associated 18

Information
Symbol
SPATA18
Type
protein-coding
Description
spermatogenesis associated 18
Entrez Gene ID
132671
Genome
hg19
Position
chr4:52,917,470-52,963,465
Genome
hg38
Position
chr4:52,051,304-52,097,299
MIM
612814 OMIM
HGNC
HGNC:29579 HGNC
Ensembl
ENSG00000163071 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
64
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
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 :
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 Mieap
SYNONYM SPETEX1
MIM 612814 OMIM
HGNC HGNC:29579 HGNC
Ensembl ENSG00000163071 Ensembl
AllianceGenome HGNC:29579
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000419395.6 hg38 chr4 52,051,416 52,095,893 44,478
ENST00000295213.9 hg38 chr4 52,051,304 52,097,299 45,996
ENST00000295213.9 hg19 chr4 52,917,470 52,963,465 45,996
ENST00000419395.6 hg19 chr4 52,917,582 52,962,059 44,478
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