RNU6-1321P
pseudogene in the species Homo sapiens
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RNU6-1321P
Summary
RNU6-1321P is a pseudogene[1].
Key Facts
- RNU6-1321P's instance of is recorded as pseudogene[2].
- RNU6-1321P's instance of is recorded as gene[3].
- RNU6-1321P is a type of pseudogene[4].
- RNU6-1321P's genomic start is recorded as 41570923[5].
- RNU6-1321P's genomic end is recorded as 41571029[6].
- RNU6-1321P's found in taxon is recorded as Homo sapiens[7].
- RNU6-1321P's chromosome is recorded as human X chromosome[8].
- RNU6-1321P's strand orientation is recorded as reverse strand[9].
- RNU6-1321P's exact match is recorded as http://identifiers.org/ncbigene/106481597[10].
- RNU6-1321P's cytogenetic location is recorded as Xp11.4[11].
- RNU6-1321P's expressed in is recorded as monocyte[12].
- RNU6-1321P's expressed in is recorded as Achilles tendon[13].
- RNU6-1321P's expressed in is recorded as blood[14].
- RNU6-1321P's expressed in is recorded as bone marrow[15].
- RNU6-1321P's expressed in is recorded as stomach[16].
- RNU6-1321P's expressed in is recorded as endometrium[17].
- RNU6-1321P's expressed in is recorded as kidney[18].
- RNU6-1321P's expressed in is recorded as fundus[19].
- RNU6-1321P's expressed in is recorded as granulocyte[20].
- RNU6-1321P's expressed in is recorded as corpus callosum[21].