RN7SL762P
pseudogene in the species Homo sapiens
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RN7SL762P
Summary
RN7SL762P is a pseudogene[1].
Key Facts
- RN7SL762P's instance of is recorded as pseudogene[2].
- RN7SL762P's instance of is recorded as gene[3].
- RN7SL762P is a type of pseudogene[4].
- RN7SL762P's genomic start is recorded as 120110498[5].
- RN7SL762P's genomic end is recorded as 120110786[6].
- RN7SL762P's found in taxon is recorded as Homo sapiens[7].
- RN7SL762P's chromosome is recorded as human chromosome 3[8].
- RN7SL762P's strand orientation is recorded as reverse strand[9].
- RN7SL762P's exact match is recorded as http://identifiers.org/ncbigene/106479500[10].
- RN7SL762P's cytogenetic location is recorded as 3q13.33[11].
- RN7SL762P's expressed in is recorded as bone marrow cell[12].
- RN7SL762P's expressed in is recorded as ventricular zone[13].
- RN7SL762P's expressed in is recorded as lymph node[14].
- RN7SL762P's expressed in is recorded as superior frontal gyrus[15].
- RN7SL762P's expressed in is recorded as white blood cell[16].
- RN7SL762P's expressed in is recorded as appendix[17].
- RN7SL762P's expressed in is recorded as liver[18].
- RN7SL762P's expressed in is recorded as prefrontal cortex[19].
- RN7SL762P's expressed in is recorded as islet of Langerhans[20].
- RN7SL762P's expressed in is recorded as monocyte[21].