RN7SL169P
pseudogene in the species Homo sapiens
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RN7SL169P
Summary
RN7SL169P is a pseudogene[1].
Key Facts
- RN7SL169P's instance of is recorded as pseudogene[2].
- RN7SL169P's instance of is recorded as gene[3].
- RN7SL169P is a type of pseudogene[4].
- RN7SL169P's genomic start is recorded as 64539504[5].
- RN7SL169P's genomic end is recorded as 64539792[6].
- RN7SL169P's found in taxon is recorded as Homo sapiens[7].
- RN7SL169P's chromosome is recorded as human chromosome 5[8].
- RN7SL169P's strand orientation is recorded as forward strand[9].
- RN7SL169P's exact match is recorded as http://identifiers.org/ncbigene/106480372[10].
- RN7SL169P's cytogenetic location is recorded as 5q12.3[11].
- RN7SL169P's expressed in is recorded as testicle[12].
- RN7SL169P's expressed in is recorded as gonad[13].
- RN7SL169P's expressed in is recorded as human kidney[14].
- RN7SL169P's expressed in is recorded as sural nerve[15].
- RN7SL169P's expressed in is recorded as liver[16].
- RN7SL169P's expressed in is recorded as stromal cell of endometrium[17].
- RN7SL169P's expressed in is recorded as monocyte[18].
- RN7SL169P's expressed in is recorded as islet of Langerhans[19].
- RN7SL169P's expressed in is recorded as prefrontal cortex[20].
- RN7SL169P's expressed in is recorded as blood[21].