U2AF1L4 U2 small nuclear RNA auxiliary factor 1 like 4

Information
Symbol
U2AF1L4
Type
protein-coding
Description
U2 small nuclear RNA auxiliary factor 1 like 4
Entrez Gene ID
199746
Genome
hg19
Position
chr19:36,233,433-36,236,346
Genome
hg38
Position
chr19:35,742,532-35,745,445
MIM
601080 OMIM
HGNC
HGNC:23020 HGNC
Ensembl
ENSG00000161265 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 42
Ranking
ClinVar
0
0
0
48
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 U2AF1-RS3
SYNONYM U2AF1L3
SYNONYM U2AF1L3V1
SYNONYM U2AF1RS3
SYNONYM U2af26
MIM 601080 OMIM
HGNC HGNC:23020 HGNC
Ensembl ENSG00000161265 Ensembl
AllianceGenome HGNC:23020
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000378975.8 hg38 chr19 35,742,527 35,745,418 2,892
ENST00000292879.9 hg38 chr19 35,742,532 35,745,445 2,914
ENST00000412391.6 hg38 chr19 35,742,529 35,745,442 2,914
ENST00000378975.8 hg19 chr19 36,233,428 36,236,319 2,892
ENST00000412391.6 hg19 chr19 36,233,430 36,236,343 2,914
ENST00000292879.9 hg19 chr19 36,233,433 36,236,346 2,914
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