RN7SL271P
pseudogene in the species Homo sapiens
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RN7SL271P
Summary
RN7SL271P is a pseudogene[1].
Key Facts
- RN7SL271P's instance of is recorded as pseudogene[2].
- RN7SL271P's instance of is recorded as gene[3].
- RN7SL271P is a type of pseudogene[4].
- RN7SL271P's genomic start is recorded as 71827177[5].
- RN7SL271P's genomic end is recorded as 71827471[6].
- RN7SL271P's found in taxon is recorded as Homo sapiens[7].
- RN7SL271P's chromosome is recorded as human chromosome 3[8].
- RN7SL271P's strand orientation is recorded as forward strand[9].
- RN7SL271P's exact match is recorded as http://identifiers.org/ncbigene/106479321[10].
- RN7SL271P's cytogenetic location is recorded as 3p13[11].
- RN7SL271P's expressed in is recorded as islet of Langerhans[12].
- RN7SL271P's expressed in is recorded as monocyte[13].
- RN7SL271P's expressed in is recorded as blood[14].
- RN7SL271P's expressed in is recorded as liver[15].
- RN7SL271P's expressed in is recorded as Brodmann area 9[16].
- RN7SL271P's expressed in is recorded as left coronary artery[17].
- RN7SL271P's expressed in is recorded as myometrium[18].
- RN7SL271P's expressed in is recorded as muscle of leg[19].
- RN7SL271P's expressed in is recorded as gastrocnemius muscle[20].
- RN7SL271P's expressed in is recorded as tibial arteries[21].