RN7SL628P
pseudogene in the species Homo sapiens
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RN7SL628P
Summary
RN7SL628P is a pseudogene[1].
Key Facts
- RN7SL628P's instance of is recorded as pseudogene[2].
- RN7SL628P's instance of is recorded as gene[3].
- RN7SL628P is a type of pseudogene[4].
- RN7SL628P's genomic start is recorded as 30612724[5].
- RN7SL628P's genomic end is recorded as 30612960[6].
- RN7SL628P's found in taxon is recorded as Homo sapiens[7].
- RN7SL628P's chromosome is recorded as human chromosome 15[8].
- RN7SL628P's strand orientation is recorded as forward strand[9].
- RN7SL628P's exact match is recorded as http://identifiers.org/ncbigene/106479451[10].
- RN7SL628P's cytogenetic location is recorded as 15q13.2[11].
- RN7SL628P's expressed in is recorded as skeletal muscle tissue[12].
- RN7SL628P's expressed in is recorded as bone marrow cell[13].
- RN7SL628P's expressed in is recorded as primary visual cortex[14].
- RN7SL628P's expressed in is recorded as prefrontal cortex[15].
- RN7SL628P's expressed in is recorded as islet of Langerhans[16].
- RN7SL628P's expressed in is recorded as urinary bladder[17].
- RN7SL628P's expressed in is recorded as blood[18].
- RN7SL628P's expressed in is recorded as monocyte[19].
- RN7SL628P's expressed in is recorded as body of pancreas[20].
- RN7SL628P's expressed in is recorded as liver[21].