SPANXD SPANX family member D

Information
Symbol
SPANXD
Type
protein-coding
Description
SPANX family member D
Entrez Gene ID
64648
Genome
hg19
Position
chrX:140,785,568-140,786,896
Genome
hg38
Position
chrX:141,697,411-141,698,739
MIM
300670 OMIM
HGNC
HGNC:14332 HGNC
Ensembl
ENSG00000196406 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
not provided 6 0
Uncertain significance 0 30
Ranking
ClinVar
0
0
0
36
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 CT11.3
SYNONYM CT11.4
SYNONYM SPANX-C
SYNONYM SPANX-D
SYNONYM SPANX-E
SYNONYM SPANXC
SYNONYM SPANXE
SYNONYM dJ171K16.1
MIM 300670 OMIM
HGNC HGNC:14332 HGNC
Ensembl ENSG00000196406 Ensembl
AllianceGenome HGNC:14332
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000370515.3 hg38 chrX 141,697,411 141,698,739 1,329
ENST00000370515.3 hg19 chrX 140,785,568 140,786,896 1,329
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