SRSF9 serine and arginine rich splicing factor 9
Information
- Symbol
- SRSF9
- Type
- protein-coding
- Description
- serine and arginine rich splicing factor 9
- Entrez Gene ID
- 8683
- Genome
- hg19
- Position
- chr12:120,899,475-120,907,551
- Genome
- hg38
- Position
- chr12:120,461,672-120,469,748
- MIM
- 601943 OMIM
- HGNC
- HGNC:10791 HGNC
- Ensembl
- ENSG00000111786 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Uncertain significance | 0 | 10 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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MGeND data only
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| 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
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| Category | : |
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| 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 | SFRS9 |
| SYNONYM | SRp30c |
| MIM | 601943 OMIM |
| HGNC | HGNC:10791 HGNC |
| Ensembl | ENSG00000111786 Ensembl |
| AllianceGenome | HGNC:10791 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000706466.1 | hg38 | chr12 | 120,461,672 | 120,469,748 | 8,077 |
| ENST00000706467.1 | hg38 | chr12 | 120,461,672 | 120,469,748 | 8,077 |
| ENST00000706469.1 | hg38 | chr12 | 120,461,672 | 120,474,773 | 13,102 |
| ENST00000229390.8 | hg38 | chr12 | 120,461,672 | 120,469,748 | 8,077 |
| ENST00000706466.1 | hg19 | chr12 | 120,899,475 | 120,907,551 | 8,077 |
| ENST00000706467.1 | hg19 | chr12 | 120,899,475 | 120,907,551 | 8,077 |
| ENST00000229390.8 | hg19 | chr12 | 120,899,475 | 120,907,551 | 8,077 |
| ENST00000706469.1 | hg19 | chr12 | 120,899,475 | 120,912,576 | 13,102 |
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