RN7SKP21
pseudogene in the species Homo sapiens
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RN7SKP21
Summary
RN7SKP21 is a pseudogene[1].
Key Facts
- RN7SKP21's instance of is recorded as pseudogene[2].
- RN7SKP21's instance of is recorded as gene[3].
- RN7SKP21 is a type of pseudogene[4].
- RN7SKP21's genomic start is recorded as 36231555[5].
- RN7SKP21's genomic end is recorded as 36231774[6].
- RN7SKP21's found in taxon is recorded as Homo sapiens[7].
- RN7SKP21's chromosome is recorded as human chromosome 14[8].
- RN7SKP21's strand orientation is recorded as reverse strand[9].
- RN7SKP21's exact match is recorded as http://identifiers.org/ncbigene/106480839[10].
- RN7SKP21's cytogenetic location is recorded as 14q13.3[11].
- RN7SKP21's expressed in is recorded as corpus callosum[12].
- RN7SKP21's expressed in is recorded as C1 segment[13].
- RN7SKP21's expressed in is recorded as prefrontal cortex[14].
- RN7SKP21's expressed in is recorded as superior frontal gyrus[15].
- RN7SKP21's expressed in is recorded as primary visual cortex[16].
- RN7SKP21's expressed in is recorded as gastrocnemius muscle[17].
- RN7SKP21's expressed in is recorded as Brodmann area 9[18].
- RN7SKP21's expressed in is recorded as substantia nigra[19].
- RN7SKP21's expressed in is recorded as hippocampus proper[20].
- RN7SKP21's expressed in is recorded as blood[21].