RN7SL199P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL199P
Summary
RN7SL199P is a pseudogene[1].
Key Facts
- RN7SL199P's instance of is recorded as pseudogene[2].
- RN7SL199P's instance of is recorded as gene[3].
- RN7SL199P is a type of pseudogene[4].
- RN7SL199P's genomic start is recorded as 46537534[5].
- RN7SL199P's genomic end is recorded as 46537814[6].
- RN7SL199P's found in taxon is recorded as Homo sapiens[7].
- RN7SL199P's chromosome is recorded as human chromosome 17[8].
- RN7SL199P's strand orientation is recorded as forward strand[9].
- RN7SL199P's exact match is recorded as http://identifiers.org/ncbigene/106480693[10].
- RN7SL199P's cytogenetic location is recorded as 17q21.31[11].
- RN7SL199P's expressed in is recorded as gonad[12].
- RN7SL199P's expressed in is recorded as testicle[13].
- RN7SL199P's expressed in is recorded as corpus callosum[14].
- RN7SL199P's expressed in is recorded as bone marrow cell[15].
- RN7SL199P's expressed in is recorded as skeletal muscle tissue[16].
- RN7SL199P's expressed in is recorded as apex of heart[17].
- RN7SL199P's expressed in is recorded as blood[18].
- RN7SL199P's expressed in is recorded as monocyte[19].
- RN7SL199P's expressed in is recorded as Achilles tendon[20].
- RN7SL199P's expressed in is recorded as primary visual cortex[21].