RN7SL687P
pseudogene in the species Homo sapiens
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RN7SL687P
Summary
RN7SL687P is a pseudogene[1].
Key Facts
- RN7SL687P's instance of is recorded as pseudogene[2].
- RN7SL687P's instance of is recorded as gene[3].
- RN7SL687P is a type of pseudogene[4].
- RN7SL687P's genomic start is recorded as 153666226[5].
- RN7SL687P's genomic end is recorded as 153666510[6].
- RN7SL687P's found in taxon is recorded as Homo sapiens[7].
- RN7SL687P's chromosome is recorded as human X chromosome[8].
- RN7SL687P's strand orientation is recorded as forward strand[9].
- RN7SL687P's exact match is recorded as http://identifiers.org/ncbigene/106481110[10].
- RN7SL687P's cytogenetic location is recorded as Xq28[11].
- RN7SL687P's expressed in is recorded as testicle[12].
- RN7SL687P's expressed in is recorded as sural nerve[13].
- RN7SL687P's expressed in is recorded as ganglionic eminence[14].
- RN7SL687P's expressed in is recorded as muscle of thigh[15].
- RN7SL687P's expressed in is recorded as tonsil[16].
- RN7SL687P's expressed in is recorded as bone marrow[17].
- RN7SL687P's expressed in is recorded as gallbladder[18].
- RN7SL687P's expressed in is recorded as human kidney[19].
- RN7SL687P's expressed in is recorded as liver[20].
- RN7SL687P's expressed in is recorded as monocyte[21].