RNU2-69P
pseudogene in the species Homo sapiens
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RNU2-69P
Summary
RNU2-69P is a pseudogene[1].
Key Facts
- RNU2-69P's instance of is recorded as pseudogene[2].
- RNU2-69P's instance of is recorded as gene[3].
- RNU2-69P is a type of pseudogene[4].
- RNU2-69P's genomic start is recorded as 58926197[5].
- RNU2-69P's genomic end is recorded as 58926296[6].
- RNU2-69P's found in taxon is recorded as Homo sapiens[7].
- RNU2-69P's chromosome is recorded as human chromosome 18[8].
- RNU2-69P's strand orientation is recorded as reverse strand[9].
- RNU2-69P's exact match is recorded as http://identifiers.org/ncbigene/106481656[10].
- RNU2-69P's cytogenetic location is recorded as 18q21.32[11].
- RNU2-69P's expressed in is recorded as endometrium[12].
- RNU2-69P's expressed in is recorded as skeletal muscle tissue[13].
- RNU2-69P's expressed in is recorded as stomach[14].
- RNU2-69P's expressed in is recorded as blood[15].
- RNU2-69P's expressed in is recorded as monocyte[16].
- RNU2-69P's expressed in is recorded as kidney[17].
- RNU2-69P's expressed in is recorded as appendix[18].
- RNU2-69P's expressed in is recorded as placenta[19].
- RNU2-69P's expressed in is recorded as lymph node[20].
- RNU2-69P's expressed in is recorded as islet of Langerhans[21].