RN7SL362P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL362P
Summary
RN7SL362P is a pseudogene[1].
Key Facts
- RN7SL362P's instance of is recorded as pseudogene[2].
- RN7SL362P's instance of is recorded as gene[3].
- RN7SL362P is a type of pseudogene[4].
- RN7SL362P's genomic start is recorded as 13715102[5].
- RN7SL362P's genomic end is recorded as 13715368[6].
- RN7SL362P's found in taxon is recorded as Homo sapiens[7].
- RN7SL362P's chromosome is recorded as human chromosome 18[8].
- RN7SL362P's strand orientation is recorded as reverse strand[9].
- RN7SL362P's exact match is recorded as http://identifiers.org/ncbigene/106481022[10].
- RN7SL362P's cytogenetic location is recorded as 18p11.21[11].
- RN7SL362P's expressed in is recorded as human kidney[12].
- RN7SL362P's expressed in is recorded as testicle[13].
- RN7SL362P's expressed in is recorded as sural nerve[14].
- RN7SL362P's expressed in is recorded as liver[15].
- RN7SL362P's expressed in is recorded as cervix[16].
- RN7SL362P's expressed in is recorded as primary visual cortex[17].
- RN7SL362P's expressed in is recorded as prefrontal cortex[18].
- RN7SL362P's expressed in is recorded as skeletal muscle tissue[19].
- RN7SL362P's expressed in is recorded as renal cortex[20].
- RN7SL362P's expressed in is recorded as bone marrow[21].