FERRY3 FERRY endosomal RAB5 effector complex subunit 3
Information
- Symbol
- FERRY3
- Type
- protein-coding
- Description
- FERRY endosomal RAB5 effector complex subunit 3
- Entrez Gene ID
- 57102
- Genome
- hg19
- Position
- chr12:4,596,901-4,647,635
- Genome
- hg38
- Position
- chr12:4,487,735-4,538,469
- MIM
- 616082 OMIM
- HGNC
- HGNC:1184 HGNC
- Ensembl
- ENSG00000047621 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 12 |
Likely pathogenic | 0 | 14 |
Benign | 0 | 4 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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4 |
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44 |
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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C12orf4 |
SYNONYM | Fy-3 |
SYNONYM | MRT66 |
MIM | 616082 OMIM |
HGNC | HGNC:1184 HGNC |
Ensembl | ENSG00000047621 Ensembl |
AllianceGenome | HGNC:1184 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000545746.5 | hg38 | chr12 | 4,489,415 | 4,538,508 | 49,094 |
ENST00000261250.8 | hg38 | chr12 | 4,487,735 | 4,538,469 | 50,735 |
ENST00000261250.8 | hg19 | chr12 | 4,596,901 | 4,647,635 | 50,735 |
ENST00000545746.5 | hg19 | chr12 | 4,598,581 | 4,647,674 | 49,094 |
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