RN7SL97P
pseudogene in the species Homo sapiens
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RN7SL97P
Summary
RN7SL97P is a pseudogene[1].
Key Facts
- RN7SL97P's instance of is recorded as pseudogene[2].
- RN7SL97P's instance of is recorded as gene[3].
- RN7SL97P is a type of pseudogene[4].
- RN7SL97P's genomic start is recorded as 25818234[5].
- RN7SL97P's genomic end is recorded as 25818532[6].
- RN7SL97P's found in taxon is recorded as Homo sapiens[7].
- RN7SL97P's chromosome is recorded as human chromosome 18[8].
- RN7SL97P's strand orientation is recorded as reverse strand[9].
- RN7SL97P's exact match is recorded as http://identifiers.org/ncbigene/106479258[10].
- RN7SL97P's cytogenetic location is recorded as 18q11.2[11].
- RN7SL97P's expressed in is recorded as epithelium of colon[12].
- RN7SL97P's expressed in is recorded as liver[13].
- RN7SL97P's expressed in is recorded as monocyte[14].
- RN7SL97P's expressed in is recorded as stomach[15].
- RN7SL97P's expressed in is recorded as blood[16].
- RN7SL97P's expressed in is recorded as gastrocnemius muscle[17].
- RN7SL97P's expressed in is recorded as left ventricle[18].
- RN7SL97P's expressed in is recorded as lung[19].
- RN7SL97P's expressed in is recorded as human kidney[20].
- RN7SL97P's expressed in is recorded as tibial arteries[21].