RNPS1 RNA binding protein with serine rich domain 1
Information
- Symbol
- RNPS1
- Type
- protein-coding
- Description
- RNA binding protein with serine rich domain 1
- Entrez Gene ID
- 10921
- Genome
- hg19
- Position
- chr16:2,303,131-2,317,604
- Genome
- hg38
- Position
- chr16:2,253,130-2,267,603
- MIM
- 606447 OMIM
- HGNC
- HGNC:10080 HGNC
- Ensembl
- ENSG00000205937 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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48 |
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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | E5.1 |
MIM | 606447 OMIM |
HGNC | HGNC:10080 HGNC |
Ensembl | ENSG00000205937 Ensembl |
AllianceGenome | HGNC:10080 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000568631.5 | hg38 | chr16 | 2,253,828 | 2,267,829 | 14,002 |
ENST00000567147.5 | hg38 | chr16 | 2,253,856 | 2,268,071 | 14,216 |
ENST00000397086.6 | hg38 | chr16 | 2,253,116 | 2,267,848 | 14,733 |
ENST00000569598.6 | hg38 | chr16 | 2,253,840 | 2,268,095 | 14,256 |
ENST00000566397.5 | hg38 | chr16 | 2,253,126 | 2,264,331 | 11,206 |
ENST00000566458.5 | hg38 | chr16 | 2,253,117 | 2,268,397 | 15,281 |
ENST00000561718.5 | hg38 | chr16 | 2,253,139 | 2,268,066 | 14,928 |
ENST00000320225.10 | hg38 | chr16 | 2,253,120 | 2,268,126 | 15,007 |
ENST00000565678.5 | hg38 | chr16 | 2,253,130 | 2,267,603 | 14,474 |
ENST00000301730.12 | hg38 | chr16 | 2,253,846 | 2,268,114 | 14,269 |
ENST00000397086.6 | hg19 | chr16 | 2,303,117 | 2,317,849 | 14,733 |
ENST00000566458.5 | hg19 | chr16 | 2,303,118 | 2,318,398 | 15,281 |
ENST00000301730.12 | hg19 | chr16 | 2,303,847 | 2,318,115 | 14,269 |
ENST00000320225.10 | hg19 | chr16 | 2,303,121 | 2,318,127 | 15,007 |
ENST00000561718.5 | hg19 | chr16 | 2,303,140 | 2,318,067 | 14,928 |
ENST00000565678.5 | hg19 | chr16 | 2,303,131 | 2,317,604 | 14,474 |
ENST00000566397.5 | hg19 | chr16 | 2,303,127 | 2,314,332 | 11,206 |
ENST00000567147.5 | hg19 | chr16 | 2,303,857 | 2,318,072 | 14,216 |
ENST00000568631.5 | hg19 | chr16 | 2,303,829 | 2,317,830 | 14,002 |
ENST00000569598.6 | hg19 | chr16 | 2,303,841 | 2,318,096 | 14,256 |
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