ARL4A ADP ribosylation factor like GTPase 4A

Information
Symbol
ARL4A
Type
protein-coding
Description
ADP ribosylation factor like GTPase 4A
Entrez Gene ID
10124
Genome
hg19
Position
chr7:12,727,258-12,730,583
Genome
hg38
Position
chr7:12,687,633-12,690,958
MIM
604786 OMIM
HGNC
HGNC:695 HGNC
Ensembl
ENSG00000122644 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
8
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
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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 ARL4
MIM 604786 OMIM
HGNC HGNC:695 HGNC
Ensembl ENSG00000122644 Ensembl
AllianceGenome HGNC:695
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000396664.2 hg38 chr7 12,686,908 12,689,176 2,269
ENST00000396663.2 hg38 chr7 12,687,286 12,690,934 3,649
ENST00000396662.5 hg38 chr7 12,686,856 12,689,179 2,324
ENST00000651779.1 hg38 chr7 12,687,633 12,690,958 3,326
ENST00000404894.1 hg38 chr7 12,687,635 12,688,914 1,280
ENST00000356797.7 hg38 chr7 12,686,908 12,689,176 2,269
ENST00000396662.5 hg19 chr7 12,726,481 12,728,804 2,324
ENST00000356797.7 hg19 chr7 12,726,533 12,728,801 2,269
ENST00000396664.2 hg19 chr7 12,726,533 12,728,801 2,269
ENST00000396663.2 hg19 chr7 12,726,911 12,730,559 3,649
ENST00000651779.1 hg19 chr7 12,727,258 12,730,583 3,326
ENST00000404894.1 hg19 chr7 12,727,260 12,728,539 1,280
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