MOB4 MOB family member 4, phocein

Information
Symbol
MOB4
Type
protein-coding
Description
MOB family member 4, phocein
Entrez Gene ID
25843
Genome
hg19
Position
chr2:198,380,790-198,418,423
Genome
hg38
Position
chr2:197,516,066-197,553,699
MIM
609361 OMIM
HGNC
HGNC:17261 HGNC
Ensembl
ENSG00000115540 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 4
Ranking
ClinVar
0
0
0
4
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 :
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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 2C4D
SYNONYM CGI-95
SYNONYM MOB1
SYNONYM MOB3
SYNONYM MOBKL3
SYNONYM PHOCN
SYNONYM PREI3
MIM 609361 OMIM
HGNC HGNC:17261 HGNC
Ensembl ENSG00000115540 Ensembl
AllianceGenome HGNC:17261
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000233892.8 hg38 chr2 197,515,571 197,553,699 38,129
ENST00000409360.1 hg38 chr2 197,516,160 197,551,279 35,120
ENST00000323303.9 hg38 chr2 197,516,066 197,553,699 37,634
ENST00000448447.6 hg38 chr2 197,516,047 197,551,012 34,966
ENST00000409916.5 hg38 chr2 197,515,581 197,550,816 35,236
ENST00000233892.8 hg19 chr2 198,380,295 198,418,423 38,129
ENST00000409916.5 hg19 chr2 198,380,305 198,415,540 35,236
ENST00000448447.6 hg19 chr2 198,380,771 198,415,736 34,966
ENST00000323303.9 hg19 chr2 198,380,790 198,418,423 37,634
ENST00000409360.1 hg19 chr2 198,380,884 198,416,003 35,120
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