MSL3 MSL complex subunit 3

Information
Symbol
MSL3
Type
protein-coding
Description
MSL complex subunit 3
Entrez Gene ID
10943
Genome
hg19
Position
chrX:11,776,356-11,793,891
Genome
hg38
Position
chrX:11,758,237-11,775,772
MIM
300609 OMIM
HGNC
HGNC:7370 HGNC
Ensembl
ENSG00000005302 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 32
Likely pathogenic 0 22
Benign 0 8
Likely benign 0 36
not provided 7 0
Uncertain significance 0 84
Ranking
ClinVar
0
0
14
156
4
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 MRSXBA
SYNONYM MRXS36
SYNONYM MRXSBA
SYNONYM MSL3L1
MIM 300609 OMIM
HGNC HGNC:7370 HGNC
Ensembl ENSG00000005302 Ensembl
AllianceGenome HGNC:7370
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000648614.1 hg38 chrX 11,759,772 11,767,960 8,189
ENST00000649685.1 hg38 chrX 11,759,634 11,775,407 15,774
ENST00000649602.1 hg38 chrX 11,759,604 11,775,736 16,133
ENST00000650628.1 hg38 chrX 11,759,648 11,775,699 16,052
ENST00000482871.6 hg38 chrX 11,760,043 11,775,677 15,635
ENST00000312196.10 hg38 chrX 11,758,237 11,775,772 17,536
ENST00000337339.7 hg38 chrX 11,758,203 11,767,977 9,775
ENST00000647857.1 hg38 chrX 11,758,250 11,769,102 10,853
ENST00000361672.6 hg38 chrX 11,758,159 11,775,747 17,589
ENST00000647869.1 hg38 chrX 11,758,205 11,775,628 17,424
ENST00000648120.1 hg38 chrX 11,758,631 11,759,320 690
ENST00000649649.1 hg38 chrX 11,759,634 11,775,720 16,087
ENST00000649797.1 hg38 chrX 11,759,687 11,767,979 8,293
ENST00000398527.7 hg38 chrX 11,758,556 11,775,726 17,171
ENST00000649851.1 hg38 chrX 11,759,657 11,767,950 8,294
ENST00000380693.8 hg38 chrX 11,759,634 11,775,726 16,093
ENST00000649078.1 hg38 chrX 11,759,424 11,775,753 16,330
ENST00000649271.1 hg38 chrX 11,760,093 11,775,731 15,639
ENST00000648013.1 hg38 chrX 11,760,048 11,775,665 15,618
ENST00000650215.1 hg38 chrX 11,759,626 11,775,731 16,106
ENST00000361672.6 hg19 chrX 11,776,278 11,793,866 17,589
ENST00000337339.7 hg19 chrX 11,776,322 11,786,096 9,775
ENST00000312196.10 hg19 chrX 11,776,356 11,793,891 17,536
ENST00000380693.8 hg19 chrX 11,777,753 11,793,845 16,093
ENST00000398527.7 hg19 chrX 11,776,675 11,793,845 17,171
ENST00000647857.1 hg19 chrX 11,776,369 11,787,221 10,853
ENST00000482871.6 hg19 chrX 11,778,162 11,793,796 15,635
ENST00000648013.1 hg19 chrX 11,778,167 11,793,784 15,618
ENST00000649271.1 hg19 chrX 11,778,212 11,793,850 15,639
ENST00000648614.1 hg19 chrX 11,777,891 11,786,079 8,189
ENST00000647869.1 hg19 chrX 11,776,324 11,793,747 17,424
ENST00000648120.1 hg19 chrX 11,776,750 11,777,439 690
ENST00000649078.1 hg19 chrX 11,777,543 11,793,872 16,330
ENST00000649602.1 hg19 chrX 11,777,723 11,793,855 16,133
ENST00000649649.1 hg19 chrX 11,777,753 11,793,839 16,087
ENST00000649685.1 hg19 chrX 11,777,753 11,793,526 15,774
ENST00000649797.1 hg19 chrX 11,777,806 11,786,098 8,293
ENST00000649851.1 hg19 chrX 11,777,776 11,786,069 8,294
ENST00000650215.1 hg19 chrX 11,777,745 11,793,850 16,106
ENST00000650628.1 hg19 chrX 11,777,767 11,793,818 16,052
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