RN7SL691P
pseudogene in the species Homo sapiens
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RN7SL691P
Summary
RN7SL691P is a pseudogene[1].
Key Facts
- RN7SL691P's instance of is recorded as pseudogene[2].
- RN7SL691P's instance of is recorded as gene[3].
- RN7SL691P is a type of pseudogene[4].
- RN7SL691P's genomic start is recorded as 43598544[5].
- RN7SL691P's genomic end is recorded as 43598844[6].
- RN7SL691P's found in taxon is recorded as Homo sapiens[7].
- RN7SL691P's chromosome is recorded as human chromosome 4[8].
- RN7SL691P's strand orientation is recorded as reverse strand[9].
- RN7SL691P's exact match is recorded as http://identifiers.org/ncbigene/106481112[10].
- RN7SL691P's cytogenetic location is recorded as 4p13[11].
- RN7SL691P's expressed in is recorded as testicle[12].
- RN7SL691P's expressed in is recorded as stomach[13].
- RN7SL691P's expressed in is recorded as human kidney[14].
- RN7SL691P's expressed in is recorded as blood[15].
- RN7SL691P's expressed in is recorded as monocyte[16].
- RN7SL691P's expressed in is recorded as tibial arteries[17].
- RN7SL691P's expressed in is recorded as lung[18].
- RN7SL691P's expressed in is recorded as liver[19].
- RN7SL691P's expressed in is recorded as ascending aorta[20].
- RN7SL691P's expressed in is recorded as putamen[21].