ARFIP2 ADP ribosylation factor interacting protein 2
Information
- Symbol
- ARFIP2
- Type
- protein-coding
- Description
- ADP ribosylation factor interacting protein 2
- Entrez Gene ID
- 23647
- Genome
- hg19
- Position
- chr11:6,495,913-6,502,709
- Genome
- hg38
- Position
- chr11:6,474,683-6,481,479
- MIM
- 601638 OMIM
- HGNC
- HGNC:17160 HGNC
- Ensembl
- ENSG00000132254 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
28 |
![]() |
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 | : |
|
Search word | : | |
Filtering | : |
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 |
Type | ID |
---|---|
SYNONYM | POR1 |
MIM | 601638 OMIM |
HGNC | HGNC:17160 HGNC |
Ensembl | ENSG00000132254 Ensembl |
AllianceGenome | HGNC:17160 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000525235.1 | hg38 | chr11 | 6,478,084 | 6,481,314 | 3,231 |
ENST00000445086.6 | hg38 | chr11 | 6,476,734 | 6,481,343 | 4,610 |
ENST00000423813.6 | hg38 | chr11 | 6,476,814 | 6,481,434 | 4,621 |
ENST00000396777.8 | hg38 | chr11 | 6,476,519 | 6,481,331 | 4,813 |
ENST00000614314.4 | hg38 | chr11 | 6,474,683 | 6,481,479 | 6,797 |
ENST00000254584.6 | hg38 | chr11 | 6,475,680 | 6,481,312 | 5,633 |
ENST00000614314.4 | hg19 | chr11 | 6,495,913 | 6,502,709 | 6,797 |
ENST00000254584.6 | hg19 | chr11 | 6,496,910 | 6,502,542 | 5,633 |
ENST00000396777.8 | hg19 | chr11 | 6,497,749 | 6,502,561 | 4,813 |
ENST00000445086.6 | hg19 | chr11 | 6,497,964 | 6,502,573 | 4,610 |
ENST00000423813.6 | hg19 | chr11 | 6,498,044 | 6,502,664 | 4,621 |
ENST00000525235.1 | hg19 | chr11 | 6,499,314 | 6,502,544 | 3,231 |
Genome browser