ITFG2 integrin alpha FG-GAP repeat containing 2

Information
Symbol
ITFG2
Type
protein-coding
Description
integrin alpha FG-GAP repeat containing 2
Entrez Gene ID
55846
Genome
hg19
Position
chr12:2,921,834-2,934,242
Genome
hg38
Position
chr12:2,812,668-2,825,076
MIM
617421 OMIM
HGNC
HGNC:30879 HGNC
Ensembl
ENSG00000111203 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
60
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 FGGAP1
SYNONYM KICS3
SYNONYM MDS028
MIM 617421 OMIM
HGNC HGNC:30879 HGNC
Ensembl ENSG00000111203 Ensembl
AllianceGenome HGNC:30879
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000228799.7 hg38 chr12 2,812,668 2,825,076 12,409
ENST00000228799.7 hg19 chr12 2,921,834 2,934,242 12,409
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