RN7SL192P
pseudogene in the species Homo sapiens
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RN7SL192P
Summary
RN7SL192P is a pseudogene[1].
Key Facts
- RN7SL192P's instance of is recorded as pseudogene[2].
- RN7SL192P's instance of is recorded as gene[3].
- RN7SL192P is a type of pseudogene[4].
- RN7SL192P's genomic start is recorded as 11011708[5].
- RN7SL192P's genomic end is recorded as 11012006[6].
- RN7SL192P's found in taxon is recorded as Homo sapiens[7].
- RN7SL192P's chromosome is recorded as human chromosome 19[8].
- RN7SL192P's strand orientation is recorded as forward strand[9].
- RN7SL192P's exact match is recorded as http://identifiers.org/ncbigene/106480974[10].
- RN7SL192P's cytogenetic location is recorded as 19p13.2[11].
- RN7SL192P's expressed in is recorded as epithelium of colon[12].
- RN7SL192P's expressed in is recorded as lymph node[13].
- RN7SL192P's expressed in is recorded as bone marrow[14].
- RN7SL192P's expressed in is recorded as bone marrow cell[15].
- RN7SL192P's expressed in is recorded as skeletal muscle tissue[16].
- RN7SL192P's expressed in is recorded as gallbladder[17].
- RN7SL192P's expressed in is recorded as monocyte[18].
- RN7SL192P's expressed in is recorded as duodenum[19].
- RN7SL192P's expressed in is recorded as islet of Langerhans[20].
- RN7SL192P's expressed in is recorded as prefrontal cortex[21].