MESP1 mesoderm posterior bHLH transcription factor 1
Information
- Symbol
- MESP1
- Type
- protein-coding
- Description
- mesoderm posterior bHLH transcription factor 1
- Entrez Gene ID
- 55897
- Genome
- hg19
- Position
- chr15:90,293,106-90,294,480
- Genome
- hg38
- Position
- chr15:89,749,875-89,751,249
- MIM
- 608689 OMIM
- HGNC
- HGNC:29658 HGNC
- Ensembl
- ENSG00000166823 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 48 |
Likely benign | 0 | 28 |
Uncertain significance | 0 | 114 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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56 |
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128 |
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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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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 | bHLHc5 |
MIM | 608689 OMIM |
HGNC | HGNC:29658 HGNC |
Ensembl | ENSG00000166823 Ensembl |
AllianceGenome | HGNC:29658 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000300057.5 | hg38 | chr15 | 89,749,875 | 89,751,249 | 1,375 |
ENST00000300057.5 | hg19 | chr15 | 90,293,106 | 90,294,480 | 1,375 |
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