ARL6IP4 ADP ribosylation factor like GTPase 6 interacting protein 4

Information
Symbol
ARL6IP4
Type
protein-coding
Description
ADP ribosylation factor like GTPase 6 interacting protein 4
Entrez Gene ID
51329
Genome
hg19
Position
chr12:123,465,228-123,467,456
Genome
hg38
Position
chr12:122,980,681-122,982,909
MIM
607668 OMIM
HGNC
HGNC:18076 HGNC
Ensembl
ENSG00000182196 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 74
Ranking
ClinVar
0
0
0
76
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 SFRS20
SYNONYM SR-25
SYNONYM SRp25
SYNONYM SRrp37
MIM 607668 OMIM
HGNC HGNC:18076 HGNC
Ensembl ENSG00000182196 Ensembl
AllianceGenome HGNC:18076
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000357866.4 hg38 chr12 122,981,140 122,982,676 1,537
ENST00000453766.7 hg38 chr12 122,980,189 122,982,909 2,721
ENST00000426960.6 hg38 chr12 122,980,263 122,982,795 2,533
ENST00000456762.3 hg38 chr12 122,981,137 122,982,731 1,595
ENST00000315580.10 hg38 chr12 122,980,681 122,982,909 2,229
ENST00000543566.6 hg38 chr12 122,980,060 122,982,913 2,854
ENST00000454885.6 hg38 chr12 122,980,495 122,982,909 2,415
ENST00000439686.6 hg38 chr12 122,980,748 122,982,706 1,959
ENST00000392435.7 hg38 chr12 122,980,191 122,982,711 2,521
ENST00000412505.6 hg38 chr12 122,980,703 122,982,860 2,158
ENST00000453766.7 hg19 chr12 123,464,736 123,467,456 2,721
ENST00000543566.6 hg19 chr12 123,464,607 123,467,460 2,854
ENST00000357866.4 hg19 chr12 123,465,687 123,467,223 1,537
ENST00000392435.7 hg19 chr12 123,464,738 123,467,258 2,521
ENST00000426960.6 hg19 chr12 123,464,810 123,467,342 2,533
ENST00000454885.6 hg19 chr12 123,465,042 123,467,456 2,415
ENST00000315580.10 hg19 chr12 123,465,228 123,467,456 2,229
ENST00000412505.6 hg19 chr12 123,465,250 123,467,407 2,158
ENST00000439686.6 hg19 chr12 123,465,295 123,467,253 1,959
ENST00000456762.3 hg19 chr12 123,465,684 123,467,278 1,595
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