RN7SL799P
pseudogene in the species Homo sapiens
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RN7SL799P
Summary
RN7SL799P is a pseudogene[1].
Key Facts
- RN7SL799P's instance of is recorded as pseudogene[2].
- RN7SL799P's instance of is recorded as gene[3].
- RN7SL799P is a type of pseudogene[4].
- RN7SL799P's genomic start is recorded as 64210691[5].
- RN7SL799P's genomic end is recorded as 64210988[6].
- RN7SL799P's found in taxon is recorded as Homo sapiens[7].
- RN7SL799P's chromosome is recorded as human X chromosome[8].
- RN7SL799P's strand orientation is recorded as forward strand[9].
- RN7SL799P's exact match is recorded as http://identifiers.org/ncbigene/106480382[10].
- RN7SL799P's cytogenetic location is recorded as Xq11.2[11].
- RN7SL799P's expressed in is recorded as sural nerve[12].
- RN7SL799P's expressed in is recorded as ganglionic eminence[13].
- RN7SL799P's expressed in is recorded as stromal cell of endometrium[14].
- RN7SL799P's expressed in is recorded as prefrontal cortex[15].
- RN7SL799P's expressed in is recorded as lymph node[16].
- RN7SL799P's expressed in is recorded as primary visual cortex[17].
- RN7SL799P's expressed in is recorded as superior frontal gyrus[18].
- RN7SL799P's expressed in is recorded as monocyte[19].
- RN7SL799P's expressed in is recorded as liver[20].
- RN7SL799P's expressed in is recorded as islet of Langerhans[21].