NONO non-POU domain containing octamer binding
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 40 |
Likely pathogenic | 0 | 14 |
Benign | 0 | 44 |
Likely benign | 0 | 68 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 100 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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24 |
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220 |
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8 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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
|
Category | : |
|
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 | MRXS34 |
SYNONYM | NMT55 |
SYNONYM | NRB54 |
SYNONYM | P54 |
SYNONYM | P54NRB |
SYNONYM | PPP1R114 |
MIM | 300084 OMIM |
HGNC | HGNC:7871 HGNC |
Ensembl | ENSG00000147140 Ensembl |
AllianceGenome | HGNC:7871 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000677879.1 | hg38 | chrX | 71,283,625 | 71,301,160 | 17,536 |
ENST00000678660.1 | hg38 | chrX | 71,283,648 | 71,301,160 | 17,513 |
ENST00000450092.6 | hg38 | chrX | 71,283,761 | 71,300,076 | 16,316 |
ENST00000677274.1 | hg38 | chrX | 71,266,029 | 71,301,160 | 35,132 |
ENST00000276079.13 | hg38 | chrX | 71,283,635 | 71,301,168 | 17,534 |
ENST00000420903.6 | hg38 | chrX | 71,283,590 | 71,301,160 | 17,571 |
ENST00000373841.5 | hg38 | chrX | 71,283,633 | 71,301,168 | 17,536 |
ENST00000454976.2 | hg38 | chrX | 71,284,194 | 71,300,076 | 15,883 |
ENST00000677612.1 | hg38 | chrX | 71,283,654 | 71,301,522 | 17,869 |
ENST00000373856.8 | hg38 | chrX | 71,283,610 | 71,300,110 | 16,501 |
ENST00000535149.5 | hg38 | chrX | 71,283,192 | 71,301,166 | 17,975 |
ENST00000676797.1 | hg38 | chrX | 71,283,641 | 71,301,522 | 17,882 |
ENST00000678830.1 | hg38 | chrX | 71,283,610 | 71,301,160 | 17,551 |
ENST00000678437.1 | hg38 | chrX | 71,283,610 | 71,301,158 | 17,549 |
ENST00000677446.1 | hg38 | chrX | 71,254,814 | 71,301,168 | 46,355 |
ENST00000678231.1 | hg38 | chrX | 71,283,652 | 71,301,160 | 17,509 |
ENST00000677446.1 | hg19 | chrX | 70,474,664 | 70,521,018 | 46,355 |
ENST00000276079.13 | hg19 | chrX | 70,503,485 | 70,521,018 | 17,534 |
ENST00000373841.5 | hg19 | chrX | 70,503,483 | 70,521,018 | 17,536 |
ENST00000373856.8 | hg19 | chrX | 70,503,460 | 70,519,960 | 16,501 |
ENST00000676797.1 | hg19 | chrX | 70,503,491 | 70,521,372 | 17,882 |
ENST00000420903.6 | hg19 | chrX | 70,503,440 | 70,521,010 | 17,571 |
ENST00000450092.6 | hg19 | chrX | 70,503,611 | 70,519,926 | 16,316 |
ENST00000677612.1 | hg19 | chrX | 70,503,504 | 70,521,372 | 17,869 |
ENST00000678231.1 | hg19 | chrX | 70,503,502 | 70,521,010 | 17,509 |
ENST00000454976.2 | hg19 | chrX | 70,504,044 | 70,519,926 | 15,883 |
ENST00000678660.1 | hg19 | chrX | 70,503,498 | 70,521,010 | 17,513 |
ENST00000677274.1 | hg19 | chrX | 70,485,879 | 70,521,010 | 35,132 |
ENST00000535149.5 | hg19 | chrX | 70,503,042 | 70,521,016 | 17,975 |
ENST00000678437.1 | hg19 | chrX | 70,503,460 | 70,521,008 | 17,549 |
ENST00000678830.1 | hg19 | chrX | 70,503,460 | 70,521,010 | 17,551 |
ENST00000677879.1 | hg19 | chrX | 70,503,475 | 70,521,010 | 17,536 |
Key | Value |
---|---|
strand | + |
start | 70,503,041 |
Gene Symbol | NONO |
Entrez GeneId | 4,841 |
Chr Band | Xq13.1 |
end | 70,521,017 |
chr | chrX |
Name | non-POU domain containing, octamer-binding |
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