RN7SL267P
pseudogene in the species Homo sapiens
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RN7SL267P
Summary
RN7SL267P is a pseudogene[1].
Key Facts
- RN7SL267P's instance of is recorded as pseudogene[2].
- RN7SL267P's instance of is recorded as gene[3].
- RN7SL267P is a type of pseudogene[4].
- RN7SL267P's genomic start is recorded as 182314284[5].
- RN7SL267P's genomic end is recorded as 182314544[6].
- RN7SL267P's found in taxon is recorded as Homo sapiens[7].
- RN7SL267P's chromosome is recorded as human chromosome 2[8].
- RN7SL267P's strand orientation is recorded as forward strand[9].
- RN7SL267P's exact match is recorded as http://identifiers.org/ncbigene/106481833[10].
- RN7SL267P's cytogenetic location is recorded as 2q32.1[11].
- RN7SL267P's expressed in is recorded as testicle[12].
- RN7SL267P's expressed in is recorded as bone marrow cell[13].
- RN7SL267P's expressed in is recorded as lymph node[14].
- RN7SL267P's expressed in is recorded as monocyte[15].
- RN7SL267P's expressed in is recorded as blood[16].
- RN7SL267P's expressed in is recorded as olfactory zone of nasal mucosa[17].
- RN7SL267P's expressed in is recorded as primary visual cortex[18].
- RN7SL267P's expressed in is recorded as islet of Langerhans[19].
- RN7SL267P's expressed in is recorded as corpus callosum[20].
- RN7SL267P's expressed in is recorded as human kidney[21].