RN7SL583P
pseudogene in the species Homo sapiens
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RN7SL583P
Summary
RN7SL583P is a pseudogene[1].
Key Facts
- RN7SL583P's instance of is recorded as pseudogene[2].
- RN7SL583P's instance of is recorded as gene[3].
- RN7SL583P is a type of pseudogene[4].
- RN7SL583P's genomic start is recorded as 88477828[5].
- RN7SL583P's genomic end is recorded as 88478114[6].
- RN7SL583P's found in taxon is recorded as Homo sapiens[7].
- RN7SL583P's chromosome is recorded as human chromosome 1[8].
- RN7SL583P's strand orientation is recorded as reverse strand[9].
- RN7SL583P's exact match is recorded as http://identifiers.org/ncbigene/106481082[10].
- RN7SL583P's cytogenetic location is recorded as 1p22.2[11].
- RN7SL583P's expressed in is recorded as lymph node[12].
- RN7SL583P's expressed in is recorded as prefrontal cortex[13].
- RN7SL583P's expressed in is recorded as bone marrow[14].
- RN7SL583P's expressed in is recorded as stromal cell of endometrium[15].
- RN7SL583P's expressed in is recorded as primary visual cortex[16].
- RN7SL583P's expressed in is recorded as human kidney[17].
- RN7SL583P's expressed in is recorded as monocyte[18].
- RN7SL583P's expressed in is recorded as liver[19].
- RN7SL583P's expressed in is recorded as hippocampus proper[20].
- RN7SL583P's expressed in is recorded as Brodmann area 9[21].