YIF1B Yip1 interacting factor homolog B, membrane trafficking protein
Information
- Symbol
- YIF1B
- Type
- protein-coding
- Description
- Yip1 interacting factor homolog B, membrane trafficking protein
- Entrez Gene ID
- 90522
- Genome
- hg19
- Position
- chr19:38,794,198-38,806,587
- Genome
- hg38
- Position
- chr19:38,303,558-38,315,947
- MIM
- 619109 OMIM
- HGNC
- HGNC:30511 HGNC
- Ensembl
- ENSG00000167645 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 12 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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66 |
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6 |
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 | FinGER8 |
SYNONYM | KABAMAS |
MIM | 619109 OMIM |
HGNC | HGNC:30511 HGNC |
Ensembl | ENSG00000167645 Ensembl |
AllianceGenome | HGNC:30511 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000592694.5 | hg38 | chr19 | 38,305,104 | 38,315,914 | 10,811 |
ENST00000392124.7 | hg38 | chr19 | 38,305,115 | 38,309,923 | 4,809 |
ENST00000591755.5 | hg38 | chr19 | 38,306,697 | 38,315,920 | 9,224 |
ENST00000592246.5 | hg38 | chr19 | 38,305,198 | 38,309,643 | 4,446 |
ENST00000591784.5 | hg38 | chr19 | 38,305,352 | 38,315,799 | 10,448 |
ENST00000329420.12 | hg38 | chr19 | 38,305,352 | 38,315,793 | 10,442 |
ENST00000337679.12 | hg38 | chr19 | 38,305,114 | 38,315,923 | 10,810 |
ENST00000339413.11 | hg38 | chr19 | 38,303,558 | 38,315,947 | 12,390 |
ENST00000339413.11 | hg19 | chr19 | 38,794,198 | 38,806,587 | 12,390 |
ENST00000592694.5 | hg19 | chr19 | 38,795,744 | 38,806,554 | 10,811 |
ENST00000337679.12 | hg19 | chr19 | 38,795,754 | 38,806,563 | 10,810 |
ENST00000392124.7 | hg19 | chr19 | 38,795,755 | 38,800,563 | 4,809 |
ENST00000592246.5 | hg19 | chr19 | 38,795,838 | 38,800,283 | 4,446 |
ENST00000329420.12 | hg19 | chr19 | 38,795,992 | 38,806,433 | 10,442 |
ENST00000591784.5 | hg19 | chr19 | 38,795,992 | 38,806,439 | 10,448 |
ENST00000591755.5 | hg19 | chr19 | 38,797,337 | 38,806,560 | 9,224 |
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