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 | |
---|---|
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0 |
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0 |
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0 |
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76 |
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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 |
Search Word
Target data | : |
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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Search word | : | |
Filtering | : |
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 |
---|---|
SYNONYM | SFRS20 |
SYNONYM | SR-25 |
SYNONYM | SRp25 |
SYNONYM | SRrp37 |
MIM | 607668 OMIM |
HGNC | HGNC:18076 HGNC |
Ensembl | ENSG00000182196 Ensembl |
AllianceGenome | HGNC:18076 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
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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