RNU7-138P
pseudogene in the species Homo sapiens
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RNU7-138P
Summary
RNU7-138P is a pseudogene[1].
Key Facts
- RNU7-138P's instance of is recorded as pseudogene[2].
- RNU7-138P's instance of is recorded as gene[3].
- RNU7-138P is a type of pseudogene[4].
- RNU7-138P's genomic start is recorded as 10744186[5].
- RNU7-138P's genomic end is recorded as 10744249[6].
- RNU7-138P's found in taxon is recorded as Homo sapiens[7].
- RNU7-138P's chromosome is recorded as human chromosome 2[8].
- RNU7-138P's strand orientation is recorded as forward strand[9].
- RNU7-138P's exact match is recorded as http://identifiers.org/ncbigene/106481801[10].
- RNU7-138P's cytogenetic location is recorded as 2p25.1[11].
- RNU7-138P's expressed in is recorded as monocyte[12].
- RNU7-138P's expressed in is recorded as intestine[13].
- RNU7-138P's expressed in is recorded as placenta[14].
- RNU7-138P's expressed in is recorded as islet of Langerhans[15].
- RNU7-138P's expressed in is recorded as vagina[16].
- RNU7-138P's expressed in is recorded as skin of abdomen[17].
- RNU7-138P's expressed in is recorded as tibial arteries[18].
- RNU7-138P's expressed in is recorded as minor salivary glands[19].
- RNU7-138P's expressed in is recorded as skin of leg[20].
- RNU7-138P's expressed in is recorded as mucosa of esophagus[21].