NOC2L NOC2 like nucleolar associated transcriptional repressor
Information
- Symbol
- NOC2L
- Type
- protein-coding
- Description
- NOC2 like nucleolar associated transcriptional repressor
- Entrez Gene ID
- 26155
- Genome
- hg19
- Position
- chr1:879,583-894,636
- Genome
- hg38
- Position
- chr1:944,203-959,256
- MIM
- 610770 OMIM
- HGNC
- HGNC:24517 HGNC
- Ensembl
- ENSG00000188976 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 22 |
Uncertain significance | 0 | 112 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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146 |
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | NET15 |
SYNONYM | NET7 |
SYNONYM | NIR |
SYNONYM | PPP1R112 |
MIM | 610770 OMIM |
HGNC | HGNC:24517 HGNC |
Ensembl | ENSG00000188976 Ensembl |
AllianceGenome | HGNC:24517 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000327044.7 | hg38 | chr1 | 944,203 | 959,256 | 15,054 |
ENST00000327044.7 | hg19 | chr1 | 879,583 | 894,636 | 15,054 |
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