MAB21L1 mab-21 like 1

Information
Symbol
MAB21L1
Type
protein-coding
Description
mab-21 like 1
Entrez Gene ID
4081
Genome
hg19
Position
chr13:36,047,556-36,052,901
Genome
hg38
Position
chr13:35,473,419-35,478,764
MIM
601280 OMIM
HGNC
HGNC:6757 HGNC
Ensembl
ENSG00000180660 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 2
Likely benign 0 4
not provided 1 0
Uncertain significance 0 18
Ranking
ClinVar
0
0
0
24
12
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 CAGR1
SYNONYM COFG
SYNONYM Nbla00126
MIM 601280 OMIM
HGNC HGNC:6757 HGNC
Ensembl ENSG00000180660 Ensembl
AllianceGenome HGNC:6757
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000707125.1 hg38 chr13 35,473,419 35,478,764 5,346
ENST00000379919.6 hg38 chr13 35,473,789 35,476,689 2,901
ENST00000707125.1 hg19 chr13 36,047,556 36,052,901 5,346
ENST00000379919.6 hg19 chr13 36,047,926 36,050,826 2,901
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