RN7SL121P
pseudogene in the species Homo sapiens
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RN7SL121P
Summary
RN7SL121P is a pseudogene[1].
Key Facts
- RN7SL121P's instance of is recorded as pseudogene[2].
- RN7SL121P's instance of is recorded as gene[3].
- RN7SL121P is a type of pseudogene[4].
- RN7SL121P's genomic start is recorded as 2595019[5].
- RN7SL121P's genomic end is recorded as 2595291[6].
- RN7SL121P's found in taxon is recorded as Homo sapiens[7].
- RN7SL121P's chromosome is recorded as human chromosome 19[8].
- RN7SL121P's strand orientation is recorded as reverse strand[9].
- RN7SL121P's exact match is recorded as http://identifiers.org/ncbigene/106479265[10].
- RN7SL121P's cytogenetic location is recorded as 19p13.3[11].
- RN7SL121P's expressed in is recorded as testicle[12].
- RN7SL121P's expressed in is recorded as lymph node[13].
- RN7SL121P's expressed in is recorded as human kidney[14].
- RN7SL121P's expressed in is recorded as bone marrow[15].
- RN7SL121P's expressed in is recorded as skeletal muscle tissue[16].
- RN7SL121P's expressed in is recorded as white blood cell[17].
- RN7SL121P's expressed in is recorded as islet of Langerhans[18].
- RN7SL121P's expressed in is recorded as placenta[19].
- RN7SL121P's expressed in is recorded as primary visual cortex[20].
- RN7SL121P's expressed in is recorded as monocyte[21].