GHRL ghrelin and obestatin prepropeptide
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 4 |
risk factor | 0 | 2 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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36 |
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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 |
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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 |
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SYNONYM | MTLRP |
MIM | 605353 OMIM |
HGNC | HGNC:18129 HGNC |
Ensembl | ENSG00000157017 Ensembl |
AllianceGenome | HGNC:18129 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000429122.1 | hg38 | chr3 | 10,285,754 | 10,292,933 | 7,180 |
ENST00000335542.13 | hg38 | chr3 | 10,285,666 | 10,292,947 | 7,282 |
ENST00000430179.5 | hg38 | chr3 | 10,285,750 | 10,292,917 | 7,168 |
ENST00000439975.6 | hg38 | chr3 | 10,285,754 | 10,292,917 | 7,164 |
ENST00000437422.6 | hg38 | chr3 | 10,285,754 | 10,292,917 | 7,164 |
ENST00000446937.2 | hg38 | chr3 | 10,285,754 | 10,292,917 | 7,164 |
ENST00000287656.11 | hg38 | chr3 | 10,285,754 | 10,292,917 | 7,164 |
ENST00000422159.5 | hg38 | chr3 | 10,285,751 | 10,290,212 | 4,462 |
ENST00000449238.6 | hg38 | chr3 | 10,285,754 | 10,292,917 | 7,164 |
ENST00000457360.5 | hg38 | chr3 | 10,285,754 | 10,292,917 | 7,164 |
ENST00000335542.13 | hg19 | chr3 | 10,327,350 | 10,334,631 | 7,282 |
ENST00000430179.5 | hg19 | chr3 | 10,327,434 | 10,334,601 | 7,168 |
ENST00000422159.5 | hg19 | chr3 | 10,327,435 | 10,331,896 | 4,462 |
ENST00000287656.11 | hg19 | chr3 | 10,327,438 | 10,334,601 | 7,164 |
ENST00000437422.6 | hg19 | chr3 | 10,327,438 | 10,334,601 | 7,164 |
ENST00000439975.6 | hg19 | chr3 | 10,327,438 | 10,334,601 | 7,164 |
ENST00000446937.2 | hg19 | chr3 | 10,327,438 | 10,334,601 | 7,164 |
ENST00000449238.6 | hg19 | chr3 | 10,327,438 | 10,334,601 | 7,164 |
ENST00000457360.5 | hg19 | chr3 | 10,327,438 | 10,334,601 | 7,164 |
ENST00000429122.1 | hg19 | chr3 | 10,327,438 | 10,334,617 | 7,180 |
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