RN7SKP22
pseudogene in the species Homo sapiens
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RN7SKP22
Summary
RN7SKP22 is a pseudogene[1].
Key Facts
- RN7SKP22's instance of is recorded as pseudogene[2].
- RN7SKP22's instance of is recorded as gene[3].
- RN7SKP22 is a type of pseudogene[4].
- RN7SKP22's genomic start is recorded as 32862800[5].
- RN7SKP22's genomic end is recorded as 32863092[6].
- RN7SKP22's found in taxon is recorded as Homo sapiens[7].
- RN7SKP22's chromosome is recorded as human chromosome 19[8].
- RN7SKP22's strand orientation is recorded as reverse strand[9].
- RN7SKP22's exact match is recorded as http://identifiers.org/ncbigene/106481805[10].
- RN7SKP22's cytogenetic location is recorded as 19q13.11[11].
- RN7SKP22's expressed in is recorded as testicle[12].
- RN7SKP22's expressed in is recorded as liver[13].
- RN7SKP22's expressed in is recorded as duodenum[14].
- RN7SKP22's expressed in is recorded as islet of Langerhans[15].
- RN7SKP22's expressed in is recorded as monocyte[16].
- RN7SKP22's expressed in is recorded as cervix[17].
- RN7SKP22's expressed in is recorded as human kidney[18].
- RN7SKP22's expressed in is recorded as primary visual cortex[19].
- RN7SKP22's expressed in is recorded as prefrontal cortex[20].
- RN7SKP22's expressed in is recorded as bone marrow[21].