RN7SL663P
pseudogene in the species Homo sapiens
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RN7SL663P
Summary
RN7SL663P is a pseudogene[1].
Key Facts
- RN7SL663P's instance of is recorded as pseudogene[2].
- RN7SL663P's instance of is recorded as gene[3].
- RN7SL663P is a type of pseudogene[4].
- RN7SL663P's genomic start is recorded as 38200234[5].
- RN7SL663P's genomic end is recorded as 38200532[6].
- RN7SL663P's found in taxon is recorded as Homo sapiens[7].
- RN7SL663P's chromosome is recorded as human chromosome 19[8].
- RN7SL663P's strand orientation is recorded as forward strand[9].
- RN7SL663P's exact match is recorded as http://identifiers.org/ncbigene/106481103[10].
- RN7SL663P's cytogenetic location is recorded as 19q13.2[11].
- RN7SL663P's expressed in is recorded as testicle[12].
- RN7SL663P's expressed in is recorded as bone marrow cell[13].
- RN7SL663P's expressed in is recorded as muscle of thigh[14].
- RN7SL663P's expressed in is recorded as right lobe of thyroid gland[15].
- RN7SL663P's expressed in is recorded as gastrocnemius muscle[16].
- RN7SL663P's expressed in is recorded as skin of leg[17].
- RN7SL663P's expressed in is recorded as skin of abdomen[18].
- RN7SL663P's expressed in is recorded as skeletal muscle tissue[19].
- RN7SL663P's expressed in is recorded as lymph node[20].
- RN7SL663P's expressed in is recorded as appendix[21].