RN7SL819P
pseudogene in the species Homo sapiens
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RN7SL819P
Summary
RN7SL819P is a pseudogene[1].
Key Facts
- RN7SL819P's instance of is recorded as pseudogene[2].
- RN7SL819P's instance of is recorded as gene[3].
- RN7SL819P is a type of pseudogene[4].
- RN7SL819P's genomic start is recorded as 44718861[5].
- RN7SL819P's genomic end is recorded as 44719130[6].
- RN7SL819P's found in taxon is recorded as Homo sapiens[7].
- RN7SL819P's chromosome is recorded as human chromosome 17[8].
- RN7SL819P's strand orientation is recorded as reverse strand[9].
- RN7SL819P's exact match is recorded as http://identifiers.org/ncbigene/106481145[10].
- RN7SL819P's cytogenetic location is recorded as 17q21.31[11].
- RN7SL819P's expressed in is recorded as bone marrow cell[12].
- RN7SL819P's expressed in is recorded as sural nerve[13].
- RN7SL819P's expressed in is recorded as testicle[14].
- RN7SL819P's expressed in is recorded as corpus callosum[15].
- RN7SL819P's expressed in is recorded as muscle of thigh[16].
- RN7SL819P's expressed in is recorded as primary visual cortex[17].
- RN7SL819P's expressed in is recorded as lymph node[18].
- RN7SL819P's expressed in is recorded as islet of Langerhans[19].
- RN7SL819P's expressed in is recorded as white blood cell[20].
- RN7SL819P's expressed in is recorded as monocyte[21].