RN7SL585P
pseudogene in the species Homo sapiens
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RN7SL585P
Summary
RN7SL585P is a pseudogene[1].
Key Facts
- RN7SL585P's instance of is recorded as pseudogene[2].
- RN7SL585P's instance of is recorded as gene[3].
- RN7SL585P is a type of pseudogene[4].
- RN7SL585P's genomic start is recorded as 94699223[5].
- RN7SL585P's genomic end is recorded as 94699502[6].
- RN7SL585P's found in taxon is recorded as Homo sapiens[7].
- RN7SL585P's chromosome is recorded as human chromosome 13[8].
- RN7SL585P's strand orientation is recorded as reverse strand[9].
- RN7SL585P's exact match is recorded as http://identifiers.org/ncbigene/106479436[10].
- RN7SL585P's cytogenetic location is recorded as 13q32.1[11].
- RN7SL585P's expressed in is recorded as ventricular zone[12].
- RN7SL585P's expressed in is recorded as ganglionic eminence[13].
- RN7SL585P's expressed in is recorded as human kidney[14].
- RN7SL585P's expressed in is recorded as liver[15].
- RN7SL585P's expressed in is recorded as primary visual cortex[16].
- RN7SL585P's expressed in is recorded as placenta[17].
- RN7SL585P's expressed in is recorded as superior frontal gyrus[18].
- RN7SL585P's expressed in is recorded as stomach[19].
- RN7SL585P's expressed in is recorded as prefrontal cortex[20].
- RN7SL585P's expressed in is recorded as blood[21].