RN7SL565P
pseudogene in the species Homo sapiens
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RN7SL565P
Summary
RN7SL565P is a pseudogene[1].
Key Facts
- RN7SL565P's instance of is recorded as pseudogene[2].
- RN7SL565P's instance of is recorded as gene[3].
- RN7SL565P is a type of pseudogene[4].
- RN7SL565P's genomic start is recorded as 41578903[5].
- RN7SL565P's genomic end is recorded as 41579186[6].
- RN7SL565P's found in taxon is recorded as Homo sapiens[7].
- RN7SL565P's chromosome is recorded as human chromosome 9[8].
- RN7SL565P's strand orientation is recorded as forward strand[9].
- RN7SL565P's exact match is recorded as http://identifiers.org/ncbigene/106481076[10].
- RN7SL565P's cytogenetic location is recorded as 9p11.2[11].
- RN7SL565P's expressed in is recorded as testicle[12].
- RN7SL565P's expressed in is recorded as primary visual cortex[13].
- RN7SL565P's expressed in is recorded as ganglionic eminence[14].
- RN7SL565P's expressed in is recorded as tonsil[15].
- RN7SL565P's expressed in is recorded as endometrium[16].
- RN7SL565P's expressed in is recorded as right lobe of liver[17].
- RN7SL565P's expressed in is recorded as appendix[18].
- RN7SL565P's expressed in is recorded as blood[19].
- RN7SL565P's expressed in is recorded as bone marrow[20].
- RN7SL565P's expressed in is recorded as monocyte[21].