MCTS1 MCTS1 re-initiation and release factor
Information
- Symbol
- MCTS1
- Type
- protein-coding
- Description
- MCTS1 re-initiation and release factor
- Entrez Gene ID
- 28985
- Genome
- hg19
- Position
- chrX:119,738,176-119,746,167
- Genome
- hg38
- Position
- chrX:120,604,321-120,612,312
- MIM
- 300587 OMIM
- HGNC
- HGNC:23357 HGNC
- Ensembl
- ENSG00000232119 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Benign | 0 | 2 |
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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8 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
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 | IMD118 |
SYNONYM | MCT-1 |
SYNONYM | MCT1 |
MIM | 300587 OMIM |
HGNC | HGNC:23357 HGNC |
Ensembl | ENSG00000232119 Ensembl |
AllianceGenome | HGNC:23357 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000371315.3 | hg38 | chrX | 120,604,321 | 120,612,312 | 7,992 |
ENST00000371317.10 | hg38 | chrX | 120,604,101 | 120,621,159 | 17,059 |
ENST00000371317.10 | hg19 | chrX | 119,737,956 | 119,755,014 | 17,059 |
ENST00000371315.3 | hg19 | chrX | 119,738,176 | 119,746,167 | 7,992 |
Key | Value |
---|---|
strand | + |
UniProt | TSG |
start | 119,737,743 |
Gene Symbol | MCTS1 |
Entrez GeneId | 28,985 |
Chr Band | Xq24 |
end | 119,755,015 |
chr | chrX |
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