RN7SL190P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL190P
Summary
RN7SL190P is a pseudogene[1].
Key Facts
- RN7SL190P's instance of is recorded as pseudogene[2].
- RN7SL190P's instance of is recorded as gene[3].
- RN7SL190P is a type of pseudogene[4].
- RN7SL190P's genomic start is recorded as 123811331[5].
- RN7SL190P's genomic end is recorded as 123811587[6].
- RN7SL190P's found in taxon is recorded as Homo sapiens[7].
- RN7SL190P's chromosome is recorded as human X chromosome[8].
- RN7SL190P's strand orientation is recorded as reverse strand[9].
- RN7SL190P's exact match is recorded as http://identifiers.org/ncbigene/106479291[10].
- RN7SL190P's cytogenetic location is recorded as Xq25[11].
- RN7SL190P's expressed in is recorded as testicle[12].
- RN7SL190P's expressed in is recorded as gonad[13].
- RN7SL190P's expressed in is recorded as bone marrow[14].
- RN7SL190P's expressed in is recorded as sural nerve[15].
- RN7SL190P's expressed in is recorded as gallbladder[16].
- RN7SL190P's expressed in is recorded as primary visual cortex[17].
- RN7SL190P's expressed in is recorded as monocyte[18].
- RN7SL190P's expressed in is recorded as prefrontal cortex[19].
- RN7SL190P's expressed in is recorded as liver[20].
- RN7SL190P's expressed in is recorded as islet of Langerhans[21].