SPANXC SPANX family member C

Information
Symbol
SPANXC
Type
protein-coding
Description
SPANX family member C
Entrez Gene ID
64663
Genome
hg19
Position
chrX:140,335,596-140,336,650
Genome
hg38
Position
chrX:141,241,463-141,242,517
MIM
300330 OMIM
HGNC
HGNC:14331 HGNC
Ensembl
ENSG00000198573 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 6 0
Ranking
ClinVar
0
0
0
4
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 CTp11
SYNONYM SPANX-C
SYNONYM SPANX-E
SYNONYM SPANXE
MIM 300330 OMIM
HGNC HGNC:14331 HGNC
Ensembl ENSG00000198573 Ensembl
AllianceGenome HGNC:14331
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000358993.3 hg38 chrX 141,241,463 141,242,517 1,055
ENST00000358993.3 hg19 chrX 140,335,596 140,336,650 1,055
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