RN7SL712P
pseudogene in the species Homo sapiens
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RN7SL712P
Summary
RN7SL712P is a pseudogene[1].
Key Facts
- RN7SL712P's instance of is recorded as pseudogene[2].
- RN7SL712P's instance of is recorded as gene[3].
- RN7SL712P is a type of pseudogene[4].
- RN7SL712P's genomic start is recorded as 115992466[5].
- RN7SL712P's genomic end is recorded as 115992773[6].
- RN7SL712P's found in taxon is recorded as Homo sapiens[7].
- RN7SL712P's chromosome is recorded as human X chromosome[8].
- RN7SL712P's strand orientation is recorded as reverse strand[9].
- RN7SL712P's exact match is recorded as http://identifiers.org/ncbigene/106481117[10].
- RN7SL712P's cytogenetic location is recorded as Xq23[11].
- RN7SL712P's expressed in is recorded as testicle[12].
- RN7SL712P's expressed in is recorded as gonad[13].
- RN7SL712P's expressed in is recorded as human kidney[14].
- RN7SL712P's expressed in is recorded as liver[15].
- RN7SL712P's expressed in is recorded as bone marrow[16].
- RN7SL712P's expressed in is recorded as amygdala[17].
- RN7SL712P's expressed in is recorded as muscle tissue[18].
- RN7SL712P's expressed in is recorded as islet of Langerhans[19].
- RN7SL712P's expressed in is recorded as stomach[20].
- RN7SL712P's expressed in is recorded as monocyte[21].