MRPS33 mitochondrial ribosomal protein S33
Information
- Symbol
- MRPS33
- Type
- protein-coding
- Description
- mitochondrial ribosomal protein S33
- Entrez Gene ID
- 51650
- Genome
- hg19
- Position
- chr7:140,702,410-140,714,752
- Genome
- hg38
- Position
- chr7:141,002,610-141,014,952
- MIM
- 611993 OMIM
- HGNC
- HGNC:16634 HGNC
- Ensembl
- ENSG00000090263 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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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 |
---|---|
SYNONYM | CGI-139 |
SYNONYM | MRP-S33 |
SYNONYM | PTD003 |
SYNONYM | S33mt |
SYNONYM | mS33 |
MIM | 611993 OMIM |
HGNC | HGNC:16634 HGNC |
Ensembl | ENSG00000090263 Ensembl |
AllianceGenome | HGNC:16634 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000324787.10 | hg38 | chr7 | 141,002,610 | 141,014,952 | 12,343 |
ENST00000469351.1 | hg38 | chr7 | 141,006,168 | 141,015,228 | 9,061 |
ENST00000393008.7 | hg38 | chr7 | 141,006,054 | 141,014,679 | 8,626 |
ENST00000496958.5 | hg38 | chr7 | 141,006,168 | 141,014,429 | 8,262 |
ENST00000467334.1 | hg38 | chr7 | 141,006,169 | 141,014,966 | 8,798 |
ENST00000324787.10 | hg19 | chr7 | 140,702,410 | 140,714,752 | 12,343 |
ENST00000393008.7 | hg19 | chr7 | 140,705,854 | 140,714,479 | 8,626 |
ENST00000496958.5 | hg19 | chr7 | 140,705,968 | 140,714,229 | 8,262 |
ENST00000469351.1 | hg19 | chr7 | 140,705,968 | 140,715,028 | 9,061 |
ENST00000467334.1 | hg19 | chr7 | 140,705,969 | 140,714,766 | 8,798 |
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