RN7SL727P
pseudogene in the species Homo sapiens
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RN7SL727P
Summary
RN7SL727P is a pseudogene[1].
Key Facts
- RN7SL727P's instance of is recorded as pseudogene[2].
- RN7SL727P's instance of is recorded as gene[3].
- RN7SL727P is a type of pseudogene[4].
- RN7SL727P's genomic start is recorded as 140085855[5].
- RN7SL727P's genomic end is recorded as 140086150[6].
- RN7SL727P's found in taxon is recorded as Homo sapiens[7].
- RN7SL727P's chromosome is recorded as human X chromosome[8].
- RN7SL727P's strand orientation is recorded as forward strand[9].
- RN7SL727P's exact match is recorded as http://identifiers.org/ncbigene/106481121[10].
- RN7SL727P's cytogenetic location is recorded as Xq27.1[11].
- RN7SL727P's expressed in is recorded as ventricular zone[12].
- RN7SL727P's expressed in is recorded as left coronary artery[13].
- RN7SL727P's expressed in is recorded as islet of Langerhans[14].
- RN7SL727P's expressed in is recorded as bone marrow[15].
- RN7SL727P's expressed in is recorded as monocyte[16].
- RN7SL727P's expressed in is recorded as liver[17].
- RN7SL727P's expressed in is recorded as appendix[18].
- RN7SL727P's expressed in is recorded as gastrocnemius muscle[19].
- RN7SL727P's expressed in is recorded as human kidney[20].
- RN7SL727P's expressed in is recorded as rectum[21].