RN7SL813P
pseudogene in the species Homo sapiens
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RN7SL813P
Summary
RN7SL813P is a pseudogene[1].
Key Facts
- RN7SL813P's instance of is recorded as pseudogene[2].
- RN7SL813P's instance of is recorded as gene[3].
- RN7SL813P is a type of pseudogene[4].
- RN7SL813P's genomic start is recorded as 168451324[5].
- RN7SL813P's genomic end is recorded as 168451606[6].
- RN7SL813P's found in taxon is recorded as Homo sapiens[7].
- RN7SL813P's chromosome is recorded as human chromosome 2[8].
- RN7SL813P's strand orientation is recorded as forward strand[9].
- RN7SL813P's exact match is recorded as http://identifiers.org/ncbigene/106480534[10].
- RN7SL813P's cytogenetic location is recorded as 2q24.3[11].
- RN7SL813P's expressed in is recorded as testicle[12].
- RN7SL813P's expressed in is recorded as sural nerve[13].
- RN7SL813P's expressed in is recorded as ganglionic eminence[14].
- RN7SL813P's expressed in is recorded as bone marrow[15].
- RN7SL813P's expressed in is recorded as corpus callosum[16].
- RN7SL813P's expressed in is recorded as monocyte[17].
- RN7SL813P's expressed in is recorded as lymph node[18].
- RN7SL813P's expressed in is recorded as primary visual cortex[19].
- RN7SL813P's expressed in is recorded as muscle tissue[20].
- RN7SL813P's expressed in is recorded as prefrontal cortex[21].