RAB11FIP4 RAB11 family interacting protein 4
Information
- Symbol
- RAB11FIP4
- Type
- protein-coding
- Description
- RAB11 family interacting protein 4
- Entrez Gene ID
- 84440
- Genome
- hg19
- Position
- chr17:29,718,693-29,865,230
- Genome
- hg38
- Position
- chr17:31,391,675-31,538,211
- MIM
- 611999 OMIM
- HGNC
- HGNC:30267 HGNC
- Ensembl
- ENSG00000131242 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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
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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 | FIP4-Rab11 |
SYNONYM | RAB11-FIP4 |
MIM | 611999 OMIM |
HGNC | HGNC:30267 HGNC |
Ensembl | ENSG00000131242 Ensembl |
AllianceGenome | HGNC:30267 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000621161.5 | hg38 | chr17 | 31,391,675 | 31,538,211 | 146,537 |
ENST00000394744.6 | hg38 | chr17 | 31,488,000 | 31,531,849 | 43,850 |
ENST00000621161.5 | hg19 | chr17 | 29,718,693 | 29,865,230 | 146,538 |
ENST00000394744.6 | hg19 | chr17 | 29,815,018 | 29,858,867 | 43,850 |
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