PRANCR progenitor renewal associated non-coding RNA
Information
- Symbol
- PRANCR
- Type
- ncRNA
- Description
- progenitor renewal associated non-coding RNA
- Entrez Gene ID
- 101928062
- Genome
- hg19
- Position
- chr12:70,631,754-70,637,185
- Genome
- hg38
- Position
- chr12:70,237,974-70,243,405
- MIM
- 619085 OMIM
- HGNC
- HGNC:51126 HGNC
- Ensembl
- ENSG00000257815 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[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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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 |
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SYNONYM | CNOT2-DT |
SYNONYM | LINC01481 |
MIM | 619085 OMIM |
HGNC | HGNC:51126 HGNC |
Ensembl | ENSG00000257815 Ensembl |
AllianceGenome | HGNC:51126 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000656495.3 | hg38 | chr12 | 70,237,974 | 70,243,405 | 5,432 |
ENST00000686072.1 | hg38 | chr12 | 70,242,286 | 70,243,398 | 1,113 |
ENST00000675475.1 | hg38 | chr12 | 70,219,131 | 70,243,376 | 24,246 |
ENST00000676451.1 | hg38 | chr12 | 70,170,945 | 70,242,844 | 71,900 |
ENST00000701960.1 | hg38 | chr12 | 70,219,132 | 70,243,353 | 24,222 |
ENST00000668518.1 | hg38 | chr12 | 69,902,099 | 70,243,337 | 341,239 |
ENST00000668518.1 | hg19 | chr12 | 70,295,879 | 70,637,117 | 341,239 |
ENST00000676451.1 | hg19 | chr12 | 70,564,725 | 70,636,624 | 71,900 |
ENST00000675475.1 | hg19 | chr12 | 70,612,911 | 70,637,156 | 24,246 |
ENST00000701960.1 | hg19 | chr12 | 70,612,912 | 70,637,133 | 24,222 |
ENST00000656495.3 | hg19 | chr12 | 70,631,754 | 70,637,185 | 5,432 |
ENST00000686072.1 | hg19 | chr12 | 70,636,066 | 70,637,178 | 1,113 |
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