RN7SL390P
pseudogene in the species Homo sapiens
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RN7SL390P
Summary
RN7SL390P is a pseudogene[1].
Key Facts
- RN7SL390P's instance of is recorded as pseudogene[2].
- RN7SL390P's instance of is recorded as gene[3].
- RN7SL390P is a type of pseudogene[4].
- RN7SL390P's genomic start is recorded as 54255627[5].
- RN7SL390P's genomic end is recorded as 54255910[6].
- RN7SL390P's found in taxon is recorded as Homo sapiens[7].
- RN7SL390P's chromosome is recorded as human chromosome 12[8].
- RN7SL390P's strand orientation is recorded as reverse strand[9].
- RN7SL390P's exact match is recorded as http://identifiers.org/ncbigene/106479366[10].
- RN7SL390P's cytogenetic location is recorded as 12q13.13[11].
- RN7SL390P's expressed in is recorded as epithelium of colon[12].
- RN7SL390P's expressed in is recorded as bone marrow cell[13].
- RN7SL390P's expressed in is recorded as gonad[14].
- RN7SL390P's expressed in is recorded as human kidney[15].
- RN7SL390P's expressed in is recorded as liver[16].
- RN7SL390P's expressed in is recorded as lung[17].
- RN7SL390P's expressed in is recorded as islet of Langerhans[18].
- RN7SL390P's expressed in is recorded as monocyte[19].
- RN7SL390P's expressed in is recorded as primary visual cortex[20].
- RN7SL390P's expressed in is recorded as muscle of leg[21].