RPS26P9
pseudogene in the species Homo sapiens
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RPS26P9
Summary
RPS26P9 is a pseudogene[1].
Key Facts
- RPS26P9's instance of is recorded as pseudogene[2].
- RPS26P9's instance of is recorded as gene[3].
- RPS26P9 is a type of pseudogene[4].
- RPS26P9's genomic start is recorded as 20616644[5].
- RPS26P9's genomic end is recorded as 20616991[6].
- RPS26P9's found in taxon is recorded as Homo sapiens[7].
- RPS26P9's chromosome is recorded as human chromosome 14[8].
- RPS26P9's strand orientation is recorded as reverse strand[9].
- RPS26P9's exact match is recorded as http://identifiers.org/ncbigene/446209[10].
- RPS26P9's cytogenetic location is recorded as 14q11.2[11].
- RPS26P9's expressed in is recorded as somatic cell[12].
- RPS26P9's expressed in is recorded as white blood cell[13].
- RPS26P9's expressed in is recorded as monocyte[14].
- RPS26P9's expressed in is recorded as substantia nigra[15].