RN7SL221P
pseudogene in the species Homo sapiens
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RN7SL221P
Summary
RN7SL221P is a pseudogene[1].
Key Facts
- RN7SL221P's instance of is recorded as pseudogene[2].
- RN7SL221P's instance of is recorded as gene[3].
- RN7SL221P is a type of pseudogene[4].
- RN7SL221P's genomic start is recorded as 5918564[5].
- RN7SL221P's genomic end is recorded as 5918844[6].
- RN7SL221P's found in taxon is recorded as Homo sapiens[7].
- RN7SL221P's chromosome is recorded as human chromosome 6[8].
- RN7SL221P's strand orientation is recorded as reverse strand[9].
- RN7SL221P's exact match is recorded as http://identifiers.org/ncbigene/106480982[10].
- RN7SL221P's cytogenetic location is recorded as 6p25.1[11].
- RN7SL221P's expressed in is recorded as gonad[12].
- RN7SL221P's expressed in is recorded as ganglionic eminence[13].
- RN7SL221P's expressed in is recorded as muscle of thigh[14].
- RN7SL221P's expressed in is recorded as primary visual cortex[15].
- RN7SL221P's expressed in is recorded as lymph node[16].
- RN7SL221P's expressed in is recorded as skeletal muscle tissue[17].
- RN7SL221P's expressed in is recorded as appendix[18].
- RN7SL221P's expressed in is recorded as mucosa of transverse colon[19].
- RN7SL221P's expressed in is recorded as islet of Langerhans[20].
- RN7SL221P's expressed in is recorded as prefrontal cortex[21].