SPANXN1 SPANX family member N1

Information
Symbol
SPANXN1
Type
protein-coding
Description
SPANX family member N1
Entrez Gene ID
494118
Genome
hg19
Position
chrX:144,329,023-144,337,728
Genome
hg38
Position
chrX:145,247,503-145,256,208
MIM
300664 OMIM
HGNC
HGNC:33174 HGNC
Ensembl
ENSG00000203923 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Uncertain significance 0 6
Ranking
ClinVar
0
0
0
6
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 CT11.6
MIM 300664 OMIM
HGNC HGNC:33174 HGNC
Ensembl ENSG00000203923 Ensembl
AllianceGenome HGNC:33174
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370493.4 hg38 chrX 145,247,503 145,256,208 8,706
ENST00000370493.4 hg19 chrX 144,329,023 144,337,728 8,706
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