RN7SL191P
pseudogene in the species Homo sapiens
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RN7SL191P
Summary
RN7SL191P is a pseudogene[1].
Key Facts
- RN7SL191P's instance of is recorded as pseudogene[2].
- RN7SL191P's instance of is recorded as gene[3].
- RN7SL191P is a type of pseudogene[4].
- RN7SL191P's genomic start is recorded as 131134086[5].
- RN7SL191P's genomic end is recorded as 131134390[6].
- RN7SL191P's found in taxon is recorded as Homo sapiens[7].
- RN7SL191P's chromosome is recorded as human X chromosome[8].
- RN7SL191P's strand orientation is recorded as reverse strand[9].
- RN7SL191P's exact match is recorded as http://identifiers.org/ncbigene/106479292[10].
- RN7SL191P's cytogenetic location is recorded as Xq26.1[11].
- RN7SL191P's expressed in is recorded as testicle[12].
- RN7SL191P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL191P's expressed in is recorded as primary visual cortex[14].
- RN7SL191P's expressed in is recorded as liver[15].
- RN7SL191P's expressed in is recorded as islet of Langerhans[16].
- RN7SL191P's expressed in is recorded as human kidney[17].
- RN7SL191P's expressed in is recorded as olfactory zone of nasal mucosa[18].
- RN7SL191P's expressed in is recorded as superior frontal gyrus[19].
- RN7SL191P's expressed in is recorded as blood[20].
- RN7SL191P's expressed in is recorded as prefrontal cortex[21].