MAB21L4 mab-21 like 4

Information
Symbol
MAB21L4
Type
protein-coding
Description
mab-21 like 4
Entrez Gene ID
79919
Genome
hg19
Position
chr2:241,825,465-241,835,573
Genome
hg38
Position
chr2:240,886,048-240,896,156
HGNC
HGNC:26216 HGNC
Ensembl
ENSG00000172478 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
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
[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 C2orf54
HGNC HGNC:26216 HGNC
Ensembl ENSG00000172478 Ensembl
AllianceGenome HGNC:26216
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000388934.5 hg38 chr2 240,886,048 240,896,156 10,109
ENST00000402775.6 hg38 chr2 240,886,048 240,892,035 5,988
ENST00000307486.12 hg38 chr2 240,886,049 240,892,038 5,990
ENST00000402775.6 hg19 chr2 241,825,465 241,831,452 5,988
ENST00000388934.5 hg19 chr2 241,825,465 241,835,573 10,109
ENST00000307486.12 hg19 chr2 241,825,466 241,831,455 5,990
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