CTR9 CTR9 homolog, Paf1/RNA polymerase II complex component
Information
- Symbol
- CTR9
- Type
- protein-coding
- Description
- CTR9 homolog, Paf1/RNA polymerase II complex component
- Entrez Gene ID
- 9646
- Genome
- hg19
- Position
- chr11:10,772,565-10,801,289
- Genome
- hg38
- Position
- chr11:10,751,018-10,779,742
- MIM
- 609366 OMIM
- HGNC
- HGNC:16850 HGNC
- Ensembl
- ENSG00000198730 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 22 |
Benign | 0 | 120 |
Likely benign | 0 | 490 |
Conflicting classifications of pathogenicity | 0 | 12 |
not provided | 0 | 2 |
Uncertain significance | 0 | 512 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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92 |
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1,028 |
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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 | SH2BP1 |
SYNONYM | TSBP |
SYNONYM | p150 |
SYNONYM | p150TSP |
MIM | 609366 OMIM |
HGNC | HGNC:16850 HGNC |
Ensembl | ENSG00000198730 Ensembl |
AllianceGenome | HGNC:16850 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000715696.1 | hg38 | chr11 | 10,751,018 | 10,779,742 | 28,725 |
ENST00000361367.7 | hg38 | chr11 | 10,751,246 | 10,779,746 | 28,501 |
ENST00000715696.1 | hg19 | chr11 | 10,772,565 | 10,801,289 | 28,725 |
ENST00000361367.7 | hg19 | chr11 | 10,772,793 | 10,801,293 | 28,501 |
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