RN7SL401P
pseudogene in the species Homo sapiens
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RN7SL401P
Summary
RN7SL401P is a pseudogene[1].
Key Facts
- RN7SL401P's instance of is recorded as pseudogene[2].
- RN7SL401P's instance of is recorded as gene[3].
- RN7SL401P is a type of pseudogene[4].
- RN7SL401P's genomic start is recorded as 73744935[5].
- RN7SL401P's genomic end is recorded as 73745232[6].
- RN7SL401P's found in taxon is recorded as Homo sapiens[7].
- RN7SL401P's chromosome is recorded as human chromosome 18[8].
- RN7SL401P's strand orientation is recorded as forward strand[9].
- RN7SL401P's exact match is recorded as http://identifiers.org/ncbigene/106480507[10].
- RN7SL401P's cytogenetic location is recorded as 18q22.3[11].
- RN7SL401P's expressed in is recorded as ganglionic eminence[12].
- RN7SL401P's expressed in is recorded as monocyte[13].
- RN7SL401P's expressed in is recorded as liver[14].
- RN7SL401P's expressed in is recorded as prefrontal cortex[15].
- RN7SL401P's expressed in is recorded as substantia nigra[16].
- RN7SL401P's expressed in is recorded as gastrocnemius muscle[17].
- RN7SL401P's expressed in is recorded as stomach[18].
- RN7SL401P's expressed in is recorded as blood[19].
- RN7SL401P's expressed in is recorded as human kidney[20].
- RN7SL401P's expressed in is recorded as body of pancreas[21].