RN7SL343P
pseudogene in the species Homo sapiens
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RN7SL343P
Summary
RN7SL343P is a pseudogene[1].
Key Facts
- RN7SL343P's instance of is recorded as pseudogene[2].
- RN7SL343P's instance of is recorded as gene[3].
- RN7SL343P is a type of pseudogene[4].
- RN7SL343P's genomic start is recorded as 42011350[5].
- RN7SL343P's genomic end is recorded as 42011610[6].
- RN7SL343P's found in taxon is recorded as Homo sapiens[7].
- RN7SL343P's chromosome is recorded as human chromosome 9[8].
- RN7SL343P's strand orientation is recorded as forward strand[9].
- RN7SL343P's exact match is recorded as http://identifiers.org/ncbigene/106481018[10].
- RN7SL343P's cytogenetic location is recorded as 9p11.2[11].
- RN7SL343P's expressed in is recorded as bone marrow cell[12].
- RN7SL343P's expressed in is recorded as blood[13].
- RN7SL343P's expressed in is recorded as islet of Langerhans[14].
- RN7SL343P's expressed in is recorded as primary visual cortex[15].
- RN7SL343P's expressed in is recorded as myometrium[16].
- RN7SL343P's expressed in is recorded as liver[17].
- RN7SL343P's expressed in is recorded as urinary bladder[18].
- RN7SL343P's expressed in is recorded as monocyte[19].
- RN7SL343P's expressed in is recorded as prefrontal cortex[20].
- RN7SL343P's expressed in is recorded as renal cortex[21].