RN7SL636P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL636P
Summary
RN7SL636P is a pseudogene[1].
Key Facts
- RN7SL636P's instance of is recorded as pseudogene[2].
- RN7SL636P's instance of is recorded as gene[3].
- RN7SL636P is a type of pseudogene[4].
- RN7SL636P's genomic start is recorded as 50429190[5].
- RN7SL636P's genomic end is recorded as 50429483[6].
- RN7SL636P's found in taxon is recorded as Homo sapiens[7].
- RN7SL636P's chromosome is recorded as human chromosome 20[8].
- RN7SL636P's strand orientation is recorded as reverse strand[9].
- RN7SL636P's exact match is recorded as http://identifiers.org/ncbigene/106481097[10].
- RN7SL636P's cytogenetic location is recorded as 20q13.13[11].
- RN7SL636P's expressed in is recorded as tonsil[12].
- RN7SL636P's expressed in is recorded as muscle tissue[13].
- RN7SL636P's expressed in is recorded as stomach[14].
- RN7SL636P's expressed in is recorded as superior frontal gyrus[15].
- RN7SL636P's expressed in is recorded as blood[16].
- RN7SL636P's expressed in is recorded as olfactory zone of nasal mucosa[17].
- RN7SL636P's expressed in is recorded as monocyte[18].
- RN7SL636P's expressed in is recorded as left ventricle[19].
- RN7SL636P's expressed in is recorded as liver[20].
- RN7SL636P's expressed in is recorded as fallopian tube[21].