RPS26P48
pseudogene in the species Homo sapiens
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RPS26P48
Summary
RPS26P48 is a pseudogene[1].
Key Facts
- RPS26P48's instance of is recorded as pseudogene[2].
- RPS26P48's instance of is recorded as gene[3].
- RPS26P48 is a type of pseudogene[4].
- RPS26P48's genomic start is recorded as 78231281[5].
- RPS26P48's genomic end is recorded as 78231619[6].
- RPS26P48's found in taxon is recorded as Homo sapiens[7].
- RPS26P48's chromosome is recorded as human chromosome 14[8].
- RPS26P48's strand orientation is recorded as reverse strand[9].
- RPS26P48's exact match is recorded as http://identifiers.org/ncbigene/100271574[10].
- RPS26P48's cytogenetic location is recorded as 14q24.3[11].
- RPS26P48's expressed in is recorded as primary visual cortex[12].
- RPS26P48's expressed in is recorded as cell[13].
- RPS26P48's expressed in is recorded as somatic cell[14].
- RPS26P48's expressed in is recorded as white blood cell[15].
- RPS26P48's expressed in is recorded as monocyte[16].
- RPS26P48's expressed in is recorded as blood[17].
- RPS26P48's expressed in is recorded as hippocampus proper[18].
- RPS26P48's expressed in is recorded as nucleus accumbens[19].