NSRP1 nuclear speckle splicing regulatory protein 1
Information
- Symbol
- NSRP1
- Type
- protein-coding
- Description
- nuclear speckle splicing regulatory protein 1
- Entrez Gene ID
- 84081
- Genome
- hg19
- Position
- chr17:28,443,834-28,513,493
- Genome
- hg38
- Position
- chr17:30,116,816-30,186,475
- MIM
- 616173 OMIM
- HGNC
- HGNC:25305 HGNC
- Ensembl
- ENSG00000126653 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 4 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 2 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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72 |
![]() |
4 |
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 | CCDC55 |
SYNONYM | HSPC095 |
SYNONYM | NEDSSBA |
SYNONYM | NSrp70 |
MIM | 616173 OMIM |
HGNC | HGNC:25305 HGNC |
Ensembl | ENSG00000126653 Ensembl |
AllianceGenome | HGNC:25305 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000612959.4 | hg38 | chr17 | 30,116,807 | 30,186,474 | 69,668 |
ENST00000479218.6 | hg38 | chr17 | 30,116,827 | 30,128,236 | 11,410 |
ENST00000584423.5 | hg38 | chr17 | 30,116,781 | 30,128,163 | 11,383 |
ENST00000247026.10 | hg38 | chr17 | 30,116,816 | 30,186,475 | 69,660 |
ENST00000584423.5 | hg19 | chr17 | 28,443,799 | 28,455,181 | 11,383 |
ENST00000247026.10 | hg19 | chr17 | 28,443,834 | 28,513,493 | 69,660 |
ENST00000479218.6 | hg19 | chr17 | 28,443,845 | 28,455,254 | 11,410 |
ENST00000612959.4 | hg19 | chr17 | 28,443,825 | 28,513,492 | 69,668 |
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