RN7SL38P
pseudogene in the species Homo sapiens
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RN7SL38P
Summary
RN7SL38P is a pseudogene[1].
Key Facts
- RN7SL38P's instance of is recorded as pseudogene[2].
- RN7SL38P's instance of is recorded as gene[3].
- RN7SL38P is a type of pseudogene[4].
- RN7SL38P's genomic start is recorded as 24706788[5].
- RN7SL38P's genomic end is recorded as 24707083[6].
- RN7SL38P's found in taxon is recorded as Homo sapiens[7].
- RN7SL38P's chromosome is recorded as human chromosome 12[8].
- RN7SL38P's strand orientation is recorded as forward strand[9].
- RN7SL38P's exact match is recorded as http://identifiers.org/ncbigene/106480932[10].
- RN7SL38P's cytogenetic location is recorded as 12p12.1[11].
- RN7SL38P's expressed in is recorded as bone marrow cell[12].
- RN7SL38P's expressed in is recorded as testicle[13].
- RN7SL38P's expressed in is recorded as liver[14].
- RN7SL38P's expressed in is recorded as epithelium of colon[15].
- RN7SL38P's expressed in is recorded as stromal cell of endometrium[16].
- RN7SL38P's expressed in is recorded as human kidney[17].
- RN7SL38P's expressed in is recorded as sural nerve[18].
- RN7SL38P's expressed in is recorded as Brodmann area 9[19].
- RN7SL38P's expressed in is recorded as monocyte[20].
- RN7SL38P's expressed in is recorded as duodenum[21].