TMEM25 transmembrane protein 25
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 76 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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80 |
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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 |
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 |
---|---|
MIM | 613934 OMIM |
HGNC | HGNC:25890 HGNC |
Ensembl | ENSG00000149582 Ensembl |
AllianceGenome | HGNC:25890 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000354064.11 | hg38 | chr11 | 118,531,202 | 118,535,828 | 4,627 |
ENST00000524725.5 | hg38 | chr11 | 118,531,390 | 118,535,829 | 4,440 |
ENST00000533102.5 | hg38 | chr11 | 118,531,202 | 118,535,833 | 4,632 |
ENST00000359862.8 | hg38 | chr11 | 118,531,088 | 118,535,832 | 4,745 |
ENST00000354284.8 | hg38 | chr11 | 118,531,199 | 118,546,484 | 15,286 |
ENST00000411589.6 | hg38 | chr11 | 118,531,041 | 118,535,835 | 4,795 |
ENST00000313236.10 | hg38 | chr11 | 118,531,192 | 118,535,829 | 4,638 |
ENST00000442938.6 | hg38 | chr11 | 118,531,088 | 118,547,280 | 16,193 |
ENST00000313236.10 | hg19 | chr11 | 118,401,907 | 118,406,544 | 4,638 |
ENST00000354284.8 | hg19 | chr11 | 118,401,914 | 118,417,199 | 15,286 |
ENST00000354064.11 | hg19 | chr11 | 118,401,917 | 118,406,543 | 4,627 |
ENST00000411589.6 | hg19 | chr11 | 118,401,756 | 118,406,550 | 4,795 |
ENST00000359862.8 | hg19 | chr11 | 118,401,803 | 118,406,547 | 4,745 |
ENST00000442938.6 | hg19 | chr11 | 118,401,803 | 118,417,995 | 16,193 |
ENST00000524725.5 | hg19 | chr11 | 118,402,105 | 118,406,544 | 4,440 |
ENST00000533102.5 | hg19 | chr11 | 118,401,917 | 118,406,548 | 4,632 |
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