RN7SL619P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL619P
Summary
RN7SL619P is a pseudogene[1].
Key Facts
- RN7SL619P's instance of is recorded as pseudogene[2].
- RN7SL619P's instance of is recorded as gene[3].
- RN7SL619P is a type of pseudogene[4].
- RN7SL619P's genomic start is recorded as 13815062[5].
- RN7SL619P's genomic end is recorded as 13815319[6].
- RN7SL619P's found in taxon is recorded as Homo sapiens[7].
- RN7SL619P's chromosome is recorded as human chromosome 19[8].
- RN7SL619P's strand orientation is recorded as reverse strand[9].
- RN7SL619P's exact match is recorded as http://identifiers.org/ncbigene/106481091[10].
- RN7SL619P's cytogenetic location is recorded as 19p13.12[11].
- RN7SL619P's expressed in is recorded as sural nerve[12].
- RN7SL619P's expressed in is recorded as testicle[13].
- RN7SL619P's expressed in is recorded as superior frontal gyrus[14].
- RN7SL619P's expressed in is recorded as liver[15].
- RN7SL619P's expressed in is recorded as monocyte[16].
- RN7SL619P's expressed in is recorded as bone marrow[17].
- RN7SL619P's expressed in is recorded as blood[18].
- RN7SL619P's expressed in is recorded as primary visual cortex[19].
- RN7SL619P's expressed in is recorded as tonsil[20].
- RN7SL619P's expressed in is recorded as islet of Langerhans[21].