MICALL2 MICAL like 2

Information
Symbol
MICALL2
Type
protein-coding
Description
MICAL like 2
Entrez Gene ID
79778
Genome
hg19
Position
chr7:1,473,995-1,499,106
Genome
hg38
Position
chr7:1,434,359-1,459,470
HGNC
HGNC:29672 HGNC
Ensembl
ENSG00000164877 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Benign 0 54
Likely benign 0 40
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 196
Ranking
ClinVar
0
0
2
286
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 :
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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 JRAB
SYNONYM MICAL-L2
HGNC HGNC:29672 HGNC
Ensembl ENSG00000164877 Ensembl
AllianceGenome HGNC:29672
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000297508.8 hg38 chr7 1,434,359 1,459,470 25,112
ENST00000297508.8 hg19 chr7 1,473,995 1,499,106 25,112
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