ARL16 ADP ribosylation factor like GTPase 16
Information
- Symbol
- ARL16
- Type
- protein-coding
- Description
- ADP ribosylation factor like GTPase 16
- Entrez Gene ID
- 339231
- Genome
- hg19
- Position
- chr17:79,648,217-79,650,827
- Genome
- hg38
- Position
- chr17:81,681,187-81,683,797
- MIM
- 619117 OMIM
- HGNC
- HGNC:27902 HGNC
- Ensembl
- ENSG00000214087 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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34 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
MIM | 619117 OMIM |
HGNC | HGNC:27902 HGNC |
Ensembl | ENSG00000214087 Ensembl |
AllianceGenome | HGNC:27902 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000574938.5 | hg38 | chr17 | 81,681,369 | 81,683,659 | 2,291 |
ENST00000622299.5 | hg38 | chr17 | 81,681,187 | 81,683,797 | 2,611 |
ENST00000576135.5 | hg38 | chr17 | 81,681,492 | 81,683,668 | 2,177 |
ENST00000570561.5 | hg38 | chr17 | 81,681,466 | 81,683,659 | 2,194 |
ENST00000573392.5 | hg38 | chr17 | 81,681,201 | 81,683,666 | 2,466 |
ENST00000573715.2 | hg38 | chr17 | 81,681,608 | 81,683,668 | 2,061 |
ENST00000622299.5 | hg19 | chr17 | 79,648,217 | 79,650,827 | 2,611 |
ENST00000573392.5 | hg19 | chr17 | 79,648,231 | 79,650,696 | 2,466 |
ENST00000574938.5 | hg19 | chr17 | 79,648,399 | 79,650,689 | 2,291 |
ENST00000570561.5 | hg19 | chr17 | 79,648,496 | 79,650,689 | 2,194 |
ENST00000576135.5 | hg19 | chr17 | 79,648,522 | 79,650,698 | 2,177 |
ENST00000573715.2 | hg19 | chr17 | 79,648,638 | 79,650,698 | 2,061 |
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