NPLOC4 NPL4 homolog, ubiquitin recognition factor
Information
- Symbol
- NPLOC4
- Type
- protein-coding
- Description
- NPL4 homolog, ubiquitin recognition factor
- Entrez Gene ID
- 55666
- Genome
- hg19
- Position
- chr17:79,523,913-79,604,138
- Genome
- hg38
- Position
- chr17:81,556,887-81,637,112
- MIM
- 606590 OMIM
- HGNC
- HGNC:18261 HGNC
- Ensembl
- ENSG00000182446 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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52 |
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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | NPL4 |
MIM | 606590 OMIM |
HGNC | HGNC:18261 HGNC |
Ensembl | ENSG00000182446 Ensembl |
AllianceGenome | HGNC:18261 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000573876.1 | hg38 | chr17 | 81,559,125 | 81,566,635 | 7,511 |
ENST00000572760.5 | hg38 | chr17 | 81,558,789 | 81,566,602 | 7,814 |
ENST00000625705.1 | hg38 | chr17 | 81,608,801 | 81,629,875 | 21,075 |
ENST00000331134.11 | hg38 | chr17 | 81,556,887 | 81,637,112 | 80,226 |
ENST00000705719.1 | hg38 | chr17 | 81,556,887 | 81,637,112 | 80,226 |
ENST00000374747.9 | hg38 | chr17 | 81,561,766 | 81,637,060 | 75,295 |
ENST00000331134.11 | hg19 | chr17 | 79,523,913 | 79,604,138 | 80,226 |
ENST00000572760.5 | hg19 | chr17 | 79,525,815 | 79,533,628 | 7,814 |
ENST00000374747.9 | hg19 | chr17 | 79,528,792 | 79,604,086 | 75,295 |
ENST00000573876.1 | hg19 | chr17 | 79,526,151 | 79,533,661 | 7,511 |
ENST00000625705.1 | hg19 | chr17 | 79,575,827 | 79,596,901 | 21,075 |
ENST00000705719.1 | hg19 | chr17 | 79,523,913 | 79,604,138 | 80,226 |
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