Cellular Component Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | cellular_component | is_active_in | ND | | 2290270 | | MGI | GO_REF:0000015 and MGI:2156816 | |
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Cellular Component Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | cellular_component | is_active_in | ND | | 2290270 | | MGI | GO_REF:0000015 and MGI:2156816 | |
PMID:10349636 | PMID:11042159 | PMID:11076861 | PMID:11217851 | PMID:12466851 | PMID:16141072 | PMID:16141073 |
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Variants in 1700116H05Rik
547 total Variants |
The following QTLs overlap with this region. | Full Report | CSV | TAB | Printer | Gviewer |
RefSeq Acc Id: | ENSMUST00000234143 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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RefSeq Acc Id: | ENSMUST00000234211 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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RefSeq Acc Id: | ENSMUST00000234925 | ||||||||||||
Type: | CODING | ||||||||||||
Position: |
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RefSeq Acc Id: | XR_001782254 | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XR_877098 | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XR_877099 | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XR_877101 | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
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Sequence: |
RefSeq Acc Id: | XR_877102 | ||||||||||||
Type: | NON-CODING | ||||||||||||
Position: |
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Sequence: |
RGD ID: | 15094943 | ||||||||
Promoter ID: | EPDNEWNC_M2821 | ||||||||
Type: | single initiation site | ||||||||
Name: | 1700116H05Rik_1 | ||||||||
Description: | RIKEN cDNA 1700116H05 gene [Source:MGISymbol;Acc:MGI:1920872] | ||||||||
SO ACC ID: | SO:0000170 | ||||||||
Source: | EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/) | ||||||||
Experiment Methods: | Single-end sequencing. | ||||||||
Position: |
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Database | Acc Id | Source(s) |
Ensembl Genes | ENSMUSG00000117497 | Ensembl |
MGD | MGI:1920872 | ENTREZGENE |
NCBI Gene | 73622 | ENTREZGENE |
PhenoGen | 1700116H05Rik | PhenoGen |