RN7SL516P
pseudogene in the species Homo sapiens
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RN7SL516P
Summary
RN7SL516P is a pseudogene[1].
Key Facts
- RN7SL516P's instance of is recorded as pseudogene[2].
- RN7SL516P's instance of is recorded as gene[3].
- RN7SL516P is a type of pseudogene[4].
- RN7SL516P's genomic start is recorded as 29681027[5].
- RN7SL516P's genomic end is recorded as 29681323[6].
- RN7SL516P's found in taxon is recorded as Homo sapiens[7].
- RN7SL516P's chromosome is recorded as human chromosome 2[8].
- RN7SL516P's strand orientation is recorded as reverse strand[9].
- RN7SL516P's exact match is recorded as http://identifiers.org/ncbigene/106479411[10].
- RN7SL516P's cytogenetic location is recorded as 2p23.2[11].
- RN7SL516P's expressed in is recorded as testicle[12].
- RN7SL516P's expressed in is recorded as ganglionic eminence[13].
- RN7SL516P's expressed in is recorded as prefrontal cortex[14].
- RN7SL516P's expressed in is recorded as lymph node[15].
- RN7SL516P's expressed in is recorded as monocyte[16].
- RN7SL516P's expressed in is recorded as islet of Langerhans[17].
- RN7SL516P's expressed in is recorded as placenta[18].
- RN7SL516P's expressed in is recorded as blood[19].
- RN7SL516P's expressed in is recorded as anterior cingulate cortex[20].
- RN7SL516P's expressed in is recorded as liver[21].