RN7SL478P
pseudogene in the species Homo sapiens
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RN7SL478P
Summary
RN7SL478P is a pseudogene[1].
Key Facts
- RN7SL478P's instance of is recorded as pseudogene[2].
- RN7SL478P's instance of is recorded as gene[3].
- RN7SL478P is a type of pseudogene[4].
- RN7SL478P's genomic start is recorded as 97998325[5].
- RN7SL478P's genomic end is recorded as 97998622[6].
- RN7SL478P's found in taxon is recorded as Homo sapiens[7].
- RN7SL478P's chromosome is recorded as human chromosome 7[8].
- RN7SL478P's strand orientation is recorded as forward strand[9].
- RN7SL478P's exact match is recorded as http://identifiers.org/ncbigene/106481053[10].
- RN7SL478P's cytogenetic location is recorded as 7q21.3[11].
- RN7SL478P's expressed in is recorded as testicle[12].
- RN7SL478P's expressed in is recorded as sural nerve[13].
- RN7SL478P's expressed in is recorded as ganglionic eminence[14].
- RN7SL478P's expressed in is recorded as monocyte[15].
- RN7SL478P's expressed in is recorded as lymph node[16].
- RN7SL478P's expressed in is recorded as prefrontal cortex[17].
- RN7SL478P's expressed in is recorded as blood[18].
- RN7SL478P's expressed in is recorded as muscle tissue[19].
- RN7SL478P's expressed in is recorded as bone marrow[20].
- RN7SL478P's expressed in is recorded as appendix[21].