RN7SL209P
pseudogene in the species Homo sapiens
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RN7SL209P
Summary
RN7SL209P is a pseudogene[1].
Key Facts
- RN7SL209P's instance of is recorded as pseudogene[2].
- RN7SL209P's instance of is recorded as gene[3].
- RN7SL209P is a type of pseudogene[4].
- RN7SL209P's genomic start is recorded as 101773238[5].
- RN7SL209P's genomic end is recorded as 101773513[6].
- RN7SL209P's found in taxon is recorded as Homo sapiens[7].
- RN7SL209P's chromosome is recorded as human chromosome 15[8].
- RN7SL209P's strand orientation is recorded as reverse strand[9].
- RN7SL209P's exact match is recorded as http://identifiers.org/ncbigene/106480494[10].
- RN7SL209P's cytogenetic location is recorded as 15q26.3[11].
- RN7SL209P's expressed in is recorded as ganglionic eminence[12].
- RN7SL209P's expressed in is recorded as bone marrow cell[13].
- RN7SL209P's expressed in is recorded as gallbladder[14].
- RN7SL209P's expressed in is recorded as stromal cell of endometrium[15].
- RN7SL209P's expressed in is recorded as prefrontal cortex[16].
- RN7SL209P's expressed in is recorded as white blood cell[17].
- RN7SL209P's expressed in is recorded as muscle of thigh[18].
- RN7SL209P's expressed in is recorded as primary visual cortex[19].
- RN7SL209P's expressed in is recorded as tibial nerve[20].
- RN7SL209P's expressed in is recorded as left testis[21].