RN7SKP272
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SKP272
Summary
RN7SKP272 is a pseudogene[1].
Key Facts
- RN7SKP272's instance of is recorded as pseudogene[2].
- RN7SKP272's instance of is recorded as gene[3].
- RN7SKP272 is a type of pseudogene[4].
- RN7SKP272's genomic start is recorded as 89987713[5].
- RN7SKP272's genomic end is recorded as 89987944[6].
- RN7SKP272's found in taxon is recorded as Homo sapiens[7].
- RN7SKP272's chromosome is recorded as human chromosome 1[8].
- RN7SKP272's strand orientation is recorded as reverse strand[9].
- RN7SKP272's exact match is recorded as http://identifiers.org/ncbigene/106479217[10].
- RN7SKP272's cytogenetic location is recorded as 1p22.2[11].
- RN7SKP272's expressed in is recorded as corpus callosum[12].
- RN7SKP272's expressed in is recorded as sural nerve[13].
- RN7SKP272's expressed in is recorded as gonad[14].
- RN7SKP272's expressed in is recorded as bone marrow cell[15].
- RN7SKP272's expressed in is recorded as primary visual cortex[16].
- RN7SKP272's expressed in is recorded as monocyte[17].
- RN7SKP272's expressed in is recorded as prefrontal cortex[18].
- RN7SKP272's expressed in is recorded as lymph node[19].
- RN7SKP272's expressed in is recorded as superior frontal gyrus[20].
- RN7SKP272's expressed in is recorded as islet of Langerhans[21].