NBDY negative regulator of P-body association
Information
- Symbol
- NBDY
- Type
- protein-coding
- Description
- negative regulator of P-body association
- Entrez Gene ID
- 550643
- Genome
- hg19
- Position
- chrX:56,755,676-56,845,612
- Genome
- hg38
- Position
- chrX:56,729,243-56,819,179
- MIM
- 300992 OMIM
- HGNC
- HGNC:50713 HGNC
- Ensembl
- ENSG00000204272 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Ranking
ClinVar | |
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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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Filtering | : |
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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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | LINC01420 |
SYNONYM | NoBody |
MIM | 300992 OMIM |
HGNC | HGNC:50713 HGNC |
Ensembl | ENSG00000204272 Ensembl |
AllianceGenome | HGNC:50713 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000637096.1 | hg38 | chrX | 56,729,241 | 56,817,569 | 88,329 |
ENST00000423617.2 | hg38 | chrX | 56,729,354 | 56,817,626 | 88,273 |
ENST00000374922.9 | hg38 | chrX | 56,729,243 | 56,819,179 | 89,937 |
ENST00000637096.1 | hg19 | chrX | 56,755,674 | 56,844,002 | 88,329 |
ENST00000374922.9 | hg19 | chrX | 56,755,676 | 56,845,612 | 89,937 |
ENST00000423617.2 | hg19 | chrX | 56,755,787 | 56,844,059 | 88,273 |
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