RN7SL65P
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SL65P
Summary
RN7SL65P is a pseudogene[1].
Key Facts
- RN7SL65P's instance of is recorded as pseudogene[2].
- RN7SL65P's instance of is recorded as gene[3].
- RN7SL65P is a type of pseudogene[4].
- RN7SL65P's genomic start is recorded as 174240143[5].
- RN7SL65P's genomic end is recorded as 174240457[6].
- RN7SL65P's found in taxon is recorded as Homo sapiens[7].
- RN7SL65P's chromosome is recorded as human chromosome 2[8].
- RN7SL65P's strand orientation is recorded as reverse strand[9].
- RN7SL65P's exact match is recorded as http://identifiers.org/ncbigene/106479247[10].
- RN7SL65P's cytogenetic location is recorded as 2q31.1[11].
- RN7SL65P's expressed in is recorded as tonsil[12].
- RN7SL65P's expressed in is recorded as epithelium of colon[13].
- RN7SL65P's expressed in is recorded as myometrium[14].
- RN7SL65P's expressed in is recorded as monocyte[15].
- RN7SL65P's expressed in is recorded as bone marrow cell[16].
- RN7SL65P's expressed in is recorded as lymph node[17].
- RN7SL65P's expressed in is recorded as prefrontal cortex[18].
- RN7SL65P's expressed in is recorded as skeletal muscle tissue[19].
- RN7SL65P's expressed in is recorded as islet of Langerhans[20].
- RN7SL65P's expressed in is recorded as left coronary artery[21].