ARL6IP6 ADP ribosylation factor like GTPase 6 interacting protein 6

Information
Symbol
ARL6IP6
Type
protein-coding
Description
ADP ribosylation factor like GTPase 6 interacting protein 6
Entrez Gene ID
151188
Genome
hg19
Position
chr2:153,575,134-153,618,910
Genome
hg38
Position
chr2:152,718,620-152,762,396
MIM
616495 OMIM
HGNC
HGNC:24048 HGNC
Ensembl
ENSG00000177917 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely pathogenic 0 2
Benign 0 4
Uncertain significance 0 44
Ranking
ClinVar
0
0
2
46
2
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 AIP-6
SYNONYM AIP6
SYNONYM PFAAP1
MIM 616495 OMIM
HGNC HGNC:24048 HGNC
Ensembl ENSG00000177917 Ensembl
AllianceGenome HGNC:24048
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000686839.1 hg38 chr2 152,717,893 152,760,764 42,872
ENST00000688012.1 hg38 chr2 152,718,461 152,760,662 42,202
ENST00000688293.1 hg38 chr2 152,717,726 152,760,662 42,937
ENST00000686080.1 hg38 chr2 152,718,597 152,761,151 42,555
ENST00000463690.2 hg38 chr2 152,719,399 152,760,595 41,197
ENST00000687504.1 hg38 chr2 152,718,461 152,760,216 41,756
ENST00000689155.1 hg38 chr2 152,717,932 152,760,890 42,959
ENST00000326446.10 hg38 chr2 152,718,620 152,762,396 43,777
ENST00000690727.1 hg38 chr2 152,717,647 152,760,890 43,244
ENST00000691523.1 hg38 chr2 152,718,324 152,760,662 42,339
ENST00000692399.1 hg38 chr2 152,718,510 152,760,662 42,153
ENST00000326446.10 hg19 chr2 153,575,134 153,618,910 43,777
ENST00000463690.2 hg19 chr2 153,575,913 153,617,109 41,197
ENST00000688012.1 hg19 chr2 153,574,975 153,617,176 42,202
ENST00000690727.1 hg19 chr2 153,574,161 153,617,404 43,244
ENST00000688293.1 hg19 chr2 153,574,240 153,617,176 42,937
ENST00000686080.1 hg19 chr2 153,575,111 153,617,665 42,555
ENST00000686839.1 hg19 chr2 153,574,407 153,617,278 42,872
ENST00000687504.1 hg19 chr2 153,574,975 153,616,730 41,756
ENST00000689155.1 hg19 chr2 153,574,446 153,617,404 42,959
ENST00000692399.1 hg19 chr2 153,575,024 153,617,176 42,153
ENST00000691523.1 hg19 chr2 153,574,838 153,617,176 42,339
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