NPM1P49
pseudogene in the species Homo sapiens
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NPM1P49
Summary
NPM1P49 is a pseudogene[1].
Key Facts
- NPM1P49's instance of is recorded as pseudogene[2].
- NPM1P49's instance of is recorded as gene[3].
- NPM1P49 is a type of pseudogene[4].
- NPM1P49's genomic start is recorded as 47438736[5].
- NPM1P49's genomic end is recorded as 47439774[6].
- NPM1P49's found in taxon is recorded as Homo sapiens[7].
- NPM1P49's chromosome is recorded as human X chromosome[8].
- NPM1P49's strand orientation is recorded as reverse strand[9].
- NPM1P49's exact match is recorded as http://identifiers.org/ncbigene/100422284[10].
- NPM1P49's cytogenetic location is recorded as Xp11.3[11].
- NPM1P49's expressed in is recorded as skeletal muscle tissue[12].
- NPM1P49's expressed in is recorded as primary visual cortex[13].
- NPM1P49's expressed in is recorded as muscle of leg[14].
- NPM1P49's expressed in is recorded as triceps surae[15].
- NPM1P49's expressed in is recorded as gastrocnemius muscle[16].
- NPM1P49's expressed in is recorded as superior frontal gyrus[17].
- NPM1P49's expressed in is recorded as cell[18].
- NPM1P49's expressed in is recorded as prefrontal cortex[19].
- NPM1P49's expressed in is recorded as islet of Langerhans[20].
- NPM1P49's expressed in is recorded as white blood cell[21].