RNU6-1069P
pseudogene in the species Homo sapiens
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RNU6-1069P
Summary
RNU6-1069P is a pseudogene[1].
Key Facts
- RNU6-1069P's instance of is recorded as pseudogene[2].
- RNU6-1069P's instance of is recorded as gene[3].
- RNU6-1069P is a type of pseudogene[4].
- RNU6-1069P's genomic start is recorded as 31802958[5].
- RNU6-1069P's genomic end is recorded as 31803090[6].
- RNU6-1069P's found in taxon is recorded as Homo sapiens[7].
- RNU6-1069P's chromosome is recorded as human chromosome 12[8].
- RNU6-1069P's strand orientation is recorded as reverse strand[9].
- RNU6-1069P's exact match is recorded as http://identifiers.org/ncbigene/106480036[10].
- RNU6-1069P's cytogenetic location is recorded as 12p11.21[11].
- RNU6-1069P's expressed in is recorded as gonad[12].
- RNU6-1069P's expressed in is recorded as blood[13].
- RNU6-1069P's expressed in is recorded as appendix[14].
- RNU6-1069P's expressed in is recorded as corpus callosum[15].
- RNU6-1069P's expressed in is recorded as placenta[16].
- RNU6-1069P's expressed in is recorded as body of pancreas[17].
- RNU6-1069P's expressed in is recorded as muscle of leg[18].
- RNU6-1069P's expressed in is recorded as endometrium[19].
- RNU6-1069P's expressed in is recorded as ascending aorta[20].
- RNU6-1069P's expressed in is recorded as liver[21].