FCGRT Fc gamma receptor and transporter
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
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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54 |
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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 |
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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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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 | FCRN |
SYNONYM | FcgammaRn |
SYNONYM | alpha-chain |
MIM | 601437 OMIM |
HGNC | HGNC:3621 HGNC |
Ensembl | ENSG00000104870 Ensembl |
AllianceGenome | HGNC:3621 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000426395.7 | hg38 | chr19 | 49,513,154 | 49,526,333 | 13,180 |
ENST00000599988.5 | hg38 | chr19 | 49,513,255 | 49,526,333 | 13,079 |
ENST00000596975.5 | hg38 | chr19 | 49,513,379 | 49,526,329 | 12,951 |
ENST00000221466.10 | hg38 | chr19 | 49,512,661 | 49,526,428 | 13,768 |
ENST00000221466.10 | hg19 | chr19 | 50,015,918 | 50,029,685 | 13,768 |
ENST00000426395.7 | hg19 | chr19 | 50,016,411 | 50,029,590 | 13,180 |
ENST00000596975.5 | hg19 | chr19 | 50,016,636 | 50,029,586 | 12,951 |
ENST00000599988.5 | hg19 | chr19 | 50,016,512 | 50,029,590 | 13,079 |
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