RN7SKP262
pseudogene in the species Homo sapiens
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RN7SKP262
Summary
RN7SKP262 is a pseudogene[1].
Key Facts
- RN7SKP262's instance of is recorded as pseudogene[2].
- RN7SKP262's instance of is recorded as gene[3].
- RN7SKP262 is a type of pseudogene[4].
- RN7SKP262's genomic start is recorded as 25779287[5].
- RN7SKP262's genomic end is recorded as 25779569[6].
- RN7SKP262's found in taxon is recorded as Homo sapiens[7].
- RN7SKP262's chromosome is recorded as human chromosome 12[8].
- RN7SKP262's strand orientation is recorded as reverse strand[9].
- RN7SKP262's exact match is recorded as http://identifiers.org/ncbigene/106479212[10].
- RN7SKP262's cytogenetic location is recorded as 12p12.1[11].
- RN7SKP262's expressed in is recorded as sural nerve[12].
- RN7SKP262's expressed in is recorded as stomach[13].
- RN7SKP262's expressed in is recorded as monocyte[14].
- RN7SKP262's expressed in is recorded as tibial arteries[15].
- RN7SKP262's expressed in is recorded as blood[16].
- RN7SKP262's expressed in is recorded as human kidney[17].
- RN7SKP262's expressed in is recorded as caudate nucleus[18].
- RN7SKP262's expressed in is recorded as mucosa of esophagus[19].
- RN7SKP262's expressed in is recorded as liver[20].
- RN7SKP262's expressed in is recorded as subcutaneous adipose tissue[21].