RN7SKP167
pseudogene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
RN7SKP167
Summary
RN7SKP167 is a pseudogene[1].
Key Facts
- RN7SKP167's instance of is recorded as pseudogene[2].
- RN7SKP167's instance of is recorded as gene[3].
- RN7SKP167 is a type of pseudogene[4].
- RN7SKP167's genomic start is recorded as 121410916[5].
- RN7SKP167's genomic end is recorded as 121411200[6].
- RN7SKP167's found in taxon is recorded as Homo sapiens[7].
- RN7SKP167's chromosome is recorded as human chromosome 10[8].
- RN7SKP167's strand orientation is recorded as forward strand[9].
- RN7SKP167's exact match is recorded as http://identifiers.org/ncbigene/106479169[10].
- RN7SKP167's cytogenetic location is recorded as 10q26.13[11].
- RN7SKP167's expressed in is recorded as sural nerve[12].
- RN7SKP167's expressed in is recorded as ganglionic eminence[13].
- RN7SKP167's expressed in is recorded as primary visual cortex[14].
- RN7SKP167's expressed in is recorded as blood[15].
- RN7SKP167's expressed in is recorded as superior frontal gyrus[16].
- RN7SKP167's expressed in is recorded as islet of Langerhans[17].
- RN7SKP167's expressed in is recorded as prefrontal cortex[18].
- RN7SKP167's expressed in is recorded as liver[19].
- RN7SKP167's expressed in is recorded as muscle of leg[20].
- RN7SKP167's expressed in is recorded as corpus callosum[21].