ILF3 interleukin enhancer binding factor 3

Information
Symbol
ILF3
Type
protein-coding
Description
interleukin enhancer binding factor 3
Entrez Gene ID
3609
Genome
hg19
Position
chr19:10,765,022-10,803,076
Genome
hg38
Position
chr19:10,654,346-10,692,400
MIM
603182 OMIM
HGNC
HGNC:6038 HGNC
Ensembl
ENSG00000129351 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Uncertain significance 0 58
Ranking
ClinVar
0
0
0
66
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 :
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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 CBTF
SYNONYM DRBF
SYNONYM DRBP76
SYNONYM MMP4
SYNONYM MPHOSPH4
SYNONYM MPP4
SYNONYM MPP4110
SYNONYM NF-AT-90
SYNONYM NF110
SYNONYM NF110b
SYNONYM NF90
SYNONYM NF90a
SYNONYM NF90b
SYNONYM NF90c
SYNONYM NF90ctv
SYNONYM NFAR
SYNONYM NFAR-1
SYNONYM NFAR-2
SYNONYM NFAR110
SYNONYM NFAR2
SYNONYM NFAR90
SYNONYM TCP110
SYNONYM TCP80
MIM 603182 OMIM
HGNC HGNC:6038 HGNC
Ensembl ENSG00000129351 Ensembl
AllianceGenome HGNC:6038
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000250241.12 hg38 chr19 10,670,537 10,685,765 15,229
ENST00000588657.6 hg38 chr19 10,654,346 10,692,400 38,055
ENST00000590261.5 hg38 chr19 10,670,606 10,689,846 19,241
ENST00000592763.5 hg38 chr19 10,670,606 10,685,765 15,160
ENST00000589998.6 hg38 chr19 10,654,346 10,685,765 31,420
ENST00000407004.8 hg38 chr19 10,654,346 10,685,765 31,420
ENST00000407004.8 hg19 chr19 10,765,022 10,796,441 31,420
ENST00000250241.12 hg19 chr19 10,781,213 10,796,441 15,229
ENST00000588657.6 hg19 chr19 10,765,022 10,803,076 38,055
ENST00000589998.6 hg19 chr19 10,765,022 10,796,441 31,420
ENST00000590261.5 hg19 chr19 10,781,282 10,800,522 19,241
ENST00000592763.5 hg19 chr19 10,781,282 10,796,441 15,160
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