RN7SL111P
pseudogene in the species Homo sapiens
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RN7SL111P
Summary
RN7SL111P is a pseudogene[1].
Key Facts
- RN7SL111P's instance of is recorded as pseudogene[2].
- RN7SL111P's instance of is recorded as gene[3].
- RN7SL111P is a type of pseudogene[4].
- RN7SL111P's genomic start is recorded as 118016385[5].
- RN7SL111P's genomic end is recorded as 118016669[6].
- RN7SL111P's found in taxon is recorded as Homo sapiens[7].
- RN7SL111P's chromosome is recorded as human chromosome 2[8].
- RN7SL111P's strand orientation is recorded as forward strand[9].
- RN7SL111P's exact match is recorded as http://identifiers.org/ncbigene/106479263[10].
- RN7SL111P's cytogenetic location is recorded as 2q14.1[11].
- RN7SL111P's expressed in is recorded as testicle[12].
- RN7SL111P's expressed in is recorded as gonad[13].
- RN7SL111P's expressed in is recorded as ganglionic eminence[14].
- RN7SL111P's expressed in is recorded as monocyte[15].
- RN7SL111P's expressed in is recorded as liver[16].
- RN7SL111P's expressed in is recorded as prefrontal cortex[17].
- RN7SL111P's expressed in is recorded as blood[18].
- RN7SL111P's expressed in is recorded as smooth muscle tissue[19].
- RN7SL111P's expressed in is recorded as islet of Langerhans[20].
- RN7SL111P's expressed in is recorded as muscle of leg[21].