RN7SL563P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL563P
Summary
RN7SL563P is a pseudogene[1].
Key Facts
- RN7SL563P's instance of is recorded as pseudogene[2].
- RN7SL563P's instance of is recorded as gene[3].
- RN7SL563P is a type of pseudogene[4].
- RN7SL563P's genomic start is recorded as 101397636[5].
- RN7SL563P's genomic end is recorded as 101397933[6].
- RN7SL563P's found in taxon is recorded as Homo sapiens[7].
- RN7SL563P's chromosome is recorded as human chromosome 8[8].
- RN7SL563P's strand orientation is recorded as reverse strand[9].
- RN7SL563P's exact match is recorded as http://identifiers.org/ncbigene/106479427[10].
- RN7SL563P's cytogenetic location is recorded as 8q22.3[11].
- RN7SL563P's expressed in is recorded as human kidney[12].
- RN7SL563P's expressed in is recorded as liver[13].
- RN7SL563P's expressed in is recorded as muscle tissue[14].
- RN7SL563P's expressed in is recorded as sural nerve[15].
- RN7SL563P's expressed in is recorded as stomach[16].
- RN7SL563P's expressed in is recorded as heart[17].
- RN7SL563P's expressed in is recorded as monocyte[18].
- RN7SL563P's expressed in is recorded as lung[19].
- RN7SL563P's expressed in is recorded as blood[20].
- RN7SL563P's expressed in is recorded as primary visual cortex[21].