SPANXN2 SPANX family member N2

Information
Symbol
SPANXN2
Type
protein-coding
Description
SPANX family member N2
Entrez Gene ID
494119
Genome
hg19
Position
chrX:142,795,055-142,803,846
Genome
hg38
Position
chrX:143,711,955-143,720,752
MIM
300665 OMIM
HGNC
HGNC:33175 HGNC
Ensembl
ENSG00000268988 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
24
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
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 CT11.7
SYNONYM SPANX-N2
MIM 300665 OMIM
HGNC HGNC:33175 HGNC
Ensembl ENSG00000268988 Ensembl
AllianceGenome HGNC:33175
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598475.2 hg38 chrX 143,711,955 143,720,752 8,798
ENST00000598475.2 hg19 chrX 142,795,055 142,803,846 8,792
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