RN7SL49P
pseudogene in the species Homo sapiens
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RN7SL49P
Summary
RN7SL49P is a pseudogene[1].
Key Facts
- RN7SL49P's instance of is recorded as pseudogene[2].
- RN7SL49P's instance of is recorded as gene[3].
- RN7SL49P is a type of pseudogene[4].
- RN7SL49P's genomic start is recorded as 45002150[5].
- RN7SL49P's genomic end is recorded as 45002447[6].
- RN7SL49P's found in taxon is recorded as Homo sapiens[7].
- RN7SL49P's chromosome is recorded as human chromosome 13[8].
- RN7SL49P's strand orientation is recorded as forward strand[9].
- RN7SL49P's exact match is recorded as http://identifiers.org/ncbigene/106480935[10].
- RN7SL49P's cytogenetic location is recorded as 13q14.12[11].
- RN7SL49P's expressed in is recorded as sural nerve[12].
- RN7SL49P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL49P's expressed in is recorded as corpus callosum[14].
- RN7SL49P's expressed in is recorded as bone marrow cell[15].
- RN7SL49P's expressed in is recorded as muscle of thigh[16].
- RN7SL49P's expressed in is recorded as ganglionic eminence[17].
- RN7SL49P's expressed in is recorded as epithelium of colon[18].
- RN7SL49P's expressed in is recorded as lymph node[19].
- RN7SL49P's expressed in is recorded as monocyte[20].
- RN7SL49P's expressed in is recorded as right hemisphere of cerebellum[21].