SPANXN4 SPANX family member N4

Information
Symbol
SPANXN4
Type
protein-coding
Description
SPANX family member N4
Entrez Gene ID
441525
Genome
hg19
Position
chrX:142,113,714-142,122,097
Genome
hg38
Position
chrX:143,025,928-143,034,311
MIM
300667 OMIM
HGNC
HGNC:33177 HGNC
Ensembl
ENSG00000189326 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 6 0
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
20
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
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 CT11.9
MIM 300667 OMIM
HGNC HGNC:33177 HGNC
Ensembl ENSG00000189326 Ensembl
AllianceGenome HGNC:33177
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370504.3 hg38 chrX 143,025,932 143,034,702 8,771
ENST00000446864.2 hg38 chrX 143,025,928 143,034,311 8,384
ENST00000446864.2 hg19 chrX 142,113,714 142,122,097 8,384
ENST00000370504.3 hg19 chrX 142,113,718 142,122,488 8,771
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