RN7SL697P
pseudogene in the species Homo sapiens
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RN7SL697P
Summary
RN7SL697P is a pseudogene[1].
Key Facts
- RN7SL697P's instance of is recorded as pseudogene[2].
- RN7SL697P's instance of is recorded as gene[3].
- RN7SL697P is a type of pseudogene[4].
- RN7SL697P's genomic start is recorded as 154495815[5].
- RN7SL697P's genomic end is recorded as 154496113[6].
- RN7SL697P's found in taxon is recorded as Homo sapiens[7].
- RN7SL697P's chromosome is recorded as human X chromosome[8].
- RN7SL697P's strand orientation is recorded as reverse strand[9].
- RN7SL697P's exact match is recorded as http://identifiers.org/ncbigene/106480526[10].
- RN7SL697P's cytogenetic location is recorded as Xq28[11].
- RN7SL697P's expressed in is recorded as bone marrow cell[12].
- RN7SL697P's expressed in is recorded as testicle[13].
- RN7SL697P's expressed in is recorded as skeletal muscle tissue[14].
- RN7SL697P's expressed in is recorded as monocyte[15].
- RN7SL697P's expressed in is recorded as corpus callosum[16].
- RN7SL697P's expressed in is recorded as muscle of thigh[17].
- RN7SL697P's expressed in is recorded as appendix[18].
- RN7SL697P's expressed in is recorded as gastrocnemius muscle[19].
- RN7SL697P's expressed in is recorded as blood[20].
- RN7SL697P's expressed in is recorded as liver[21].