RN7SL176P
pseudogene in the species Homo sapiens
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RN7SL176P
Summary
RN7SL176P is a pseudogene[1].
Key Facts
- RN7SL176P's instance of is recorded as pseudogene[2].
- RN7SL176P's instance of is recorded as gene[3].
- RN7SL176P is a type of pseudogene[4].
- RN7SL176P's genomic start is recorded as 100158502[5].
- RN7SL176P's genomic end is recorded as 100158765[6].
- RN7SL176P's found in taxon is recorded as Homo sapiens[7].
- RN7SL176P's chromosome is recorded as human chromosome 12[8].
- RN7SL176P's strand orientation is recorded as reverse strand[9].
- RN7SL176P's exact match is recorded as http://identifiers.org/ncbigene/106480968[10].
- RN7SL176P's cytogenetic location is recorded as 12q23.1[11].
- RN7SL176P's expressed in is recorded as placenta[12].
- RN7SL176P's expressed in is recorded as monocyte[13].
- RN7SL176P's expressed in is recorded as lymph node[14].
- RN7SL176P's expressed in is recorded as tonsil[15].
- RN7SL176P's expressed in is recorded as duodenum[16].
- RN7SL176P's expressed in is recorded as prefrontal cortex[17].
- RN7SL176P's expressed in is recorded as human kidney[18].
- RN7SL176P's expressed in is recorded as islet of Langerhans[19].
- RN7SL176P's expressed in is recorded as blood[20].
- RN7SL176P's expressed in is recorded as left adrenal cortex[21].