RN7SL503P
pseudogene in the species Homo sapiens
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RN7SL503P
Summary
RN7SL503P is a pseudogene[1].
Key Facts
- RN7SL503P's instance of is recorded as pseudogene[2].
- RN7SL503P's instance of is recorded as gene[3].
- RN7SL503P is a type of pseudogene[4].
- RN7SL503P's genomic start is recorded as 35292196[5].
- RN7SL503P's genomic end is recorded as 35292498[6].
- RN7SL503P's found in taxon is recorded as Homo sapiens[7].
- RN7SL503P's chromosome is recorded as human chromosome 1[8].
- RN7SL503P's strand orientation is recorded as reverse strand[9].
- RN7SL503P's exact match is recorded as http://identifiers.org/ncbigene/106481060[10].
- RN7SL503P's cytogenetic location is recorded as 1p34.3[11].
- RN7SL503P's expressed in is recorded as bone marrow cell[12].
- RN7SL503P's expressed in is recorded as testicle[13].
- RN7SL503P's expressed in is recorded as epithelium of colon[14].
- RN7SL503P's expressed in is recorded as tonsil[15].
- RN7SL503P's expressed in is recorded as skeletal muscle tissue[16].
- RN7SL503P's expressed in is recorded as renal cortex[17].
- RN7SL503P's expressed in is recorded as blood[18].
- RN7SL503P's expressed in is recorded as primary visual cortex[19].
- RN7SL503P's expressed in is recorded as prefrontal cortex[20].
- RN7SL503P's expressed in is recorded as muscle of leg[21].