Gene: HNRNPA1P25 (heterogeneous nuclear ribonucleoprotein A1 pseudogene 25) Homo sapiens |
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Analyze |
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Symbol: |
HNRNPA1P25 |
Name: |
heterogeneous nuclear ribonucleoprotein A1 pseudogene 25 |
RGD ID: |
5013922 |
HGNC Page |
HGNC:39543 |
Description: |
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Type: |
pseudo (Ensembl: processed_pseudogene)
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RefSeq Status: |
INFERRED |
Latest Assembly: |
GRCh38 - Human Genome Assembly GRCh38 |
Position: |
Human Assembly | Chr | Position (strand) | Source | Genome Browsers |
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JBrowse | NCBI | UCSC | Ensembl |
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GRCh38 | X | 74,472,680 - 74,474,013 (-) | NCBI | GRCh38 | GRCh38 | hg38 | GRCh38 | GRCh38.p14 Ensembl | X | 74,473,017 - 74,473,953 (-) | Ensembl | GRCh38 | | hg38 | GRCh38 | GRCh37 | X | 73,692,515 - 73,693,848 (-) | NCBI | GRCh37 | GRCh37 | hg19 | GRCh37 | Build 36 | X | 73,609,575 - 73,667,308 (-) | NCBI | NCBI36 | Build 36 | hg18 | NCBI36 | Celera | X | 73,976,428 - 73,977,360 (-) | NCBI | | Celera | | | Cytogenetic Map | X | q13.2 | NCBI | | | | | HuRef | X | 67,327,301 - 67,328,647 (-) | NCBI | | HuRef | | | CHM1_1 | X | 73,585,410 - 73,586,756 (-) | NCBI | | CHM1_1 | | | T2T-CHM13v2.0 | X | 72,906,315 - 72,907,647 (-) | NCBI | | T2T-CHM13v2.0 | | |
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JBrowse: |
View Region in Genome Browser (JBrowse)
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Model |
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References
Genomics
miRNA Target Status
Predicted Target Of
Count of predictions: | 184 | Count of miRNA genes: | 172 | Interacting mature miRNAs: | 177 | Transcripts: | ENST00000422644 | Prediction methods: | Miranda, Rnahybrid | Result types: | miRGate_prediction | |
Markers in Region
DXS128 |
Human Assembly | Chr | Position (strand) | Source | JBrowse |
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GRCh37 | X | 73,836,138 - 73,836,302 | UniSTS | GRCh37 | GRCh37 | X | 73,753,323 - 73,753,666 | UniSTS | GRCh37 | GRCh37 | X | 73,746,411 - 73,746,623 | UniSTS | GRCh37 | GRCh37 | X | 73,656,093 - 73,656,283 | UniSTS | GRCh37 | Build 36 | X | 73,572,818 - 73,573,008 | RGD | NCBI36 | Celera | X | 74,029,996 - 74,030,208 | UniSTS | | Celera | X | 74,119,604 - 74,119,768 | UniSTS | | Celera | X | 74,036,906 - 74,037,249 | UniSTS | | Celera | X | 73,939,525 - 73,939,715 | RGD | | Cytogenetic Map | X | q13.2 | UniSTS | | HuRef | X | 67,471,021 - 67,471,185 | UniSTS | | HuRef | X | 67,388,419 - 67,388,762 | UniSTS | | HuRef | X | 67,381,616 - 67,381,828 | UniSTS | | HuRef | X | 67,291,441 - 67,291,631 | UniSTS | | Whitehead-YAC Contig Map | X | | UniSTS | | GeneMap99-G3 RH Map | X | 2007.0 | UniSTS | |
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GDB:600880 |
Human Assembly | Chr | Position (strand) | Source | JBrowse |
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GRCh37 | X | 73,740,901 - 73,740,988 | UniSTS | GRCh37 | Build 36 | X | 73,657,626 - 73,657,713 | RGD | NCBI36 | Celera | X | 74,024,486 - 74,024,573 | RGD | | Cytogenetic Map | X | q13.2 | UniSTS | | HuRef | X | 67,376,273 - 67,376,360 | UniSTS | |
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Expression
RNA-SEQ Expression
High: > 1000 TPM value
Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM
Below Cutoff: < 0.5 TPM
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alimentary part of gastrointestinal system |
circulatory system |
endocrine system |
exocrine system |
hemolymphoid system |
hepatobiliary system |
integumental system |
musculoskeletal system |
nervous system |
renal system |
reproductive system |
respiratory system |
sensory system |
adipose tissue |
appendage |
entire extraembryonic component |
High |
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Medium |
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Low |
17
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10
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4
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4
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59
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4
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11
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2
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27
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12
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26
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3
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9
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Below cutoff |
771
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835
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609
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143
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342
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92
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1501
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603
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1288
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93
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494
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606
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58
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437
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998
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2
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Sequence
RefSeq Acc Id: |
ENST00000422644 |
Type: |
CODING |
Position: |
Human Assembly | Chr | Position (strand) | Source |
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GRCh38.p14 Ensembl | X | 74,473,017 - 74,473,953 (-) | Ensembl |
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Additional Information
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