MAB21L2 mab-21 like 2

Information
Symbol
MAB21L2
Type
protein-coding
Description
mab-21 like 2
Entrez Gene ID
10586
Genome
hg19
Position
chr4:151,503,303-151,505,845
Genome
hg38
Position
chr4:150,582,151-150,584,693
MIM
604357 OMIM
HGNC
HGNC:6758 HGNC
Ensembl
ENSG00000181541 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 6
Likely pathogenic 0 14
Benign 0 8
Likely benign 0 22
Uncertain significance 0 24
Ranking
ClinVar
0
0
8
64
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
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 MCOPS14
SYNONYM MCSKS14
MIM 604357 OMIM
HGNC HGNC:6758 HGNC
Ensembl ENSG00000181541 Ensembl
AllianceGenome HGNC:6758
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000317605.6 hg38 chr4 150,582,151 150,584,693 2,543
ENST00000317605.6 hg19 chr4 151,503,303 151,505,845 2,543
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