RN7SKP98
pseudogene in the species Homo sapiens
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RN7SKP98
Summary
RN7SKP98 is a pseudogene[1].
Key Facts
- RN7SKP98's instance of is recorded as pseudogene[2].
- RN7SKP98's instance of is recorded as gene[3].
- RN7SKP98 is a type of pseudogene[4].
- RN7SKP98's genomic start is recorded as 212099521[5].
- RN7SKP98's genomic end is recorded as 212099676[6].
- RN7SKP98's found in taxon is recorded as Homo sapiens[7].
- RN7SKP98's chromosome is recorded as human chromosome 1[8].
- RN7SKP98's strand orientation is recorded as reverse strand[9].
- RN7SKP98's exact match is recorded as http://identifiers.org/ncbigene/106480863[10].
- RN7SKP98's cytogenetic location is recorded as 1q32.3[11].
- RN7SKP98's expressed in is recorded as ganglionic eminence[12].
- RN7SKP98's expressed in is recorded as liver[13].
- RN7SKP98's expressed in is recorded as human kidney[14].
- RN7SKP98's expressed in is recorded as small intestine[15].
- RN7SKP98's expressed in is recorded as stomach[16].
- RN7SKP98's expressed in is recorded as blood[17].
- RN7SKP98's expressed in is recorded as bone marrow[18].
- RN7SKP98's expressed in is recorded as heart[19].
- RN7SKP98's expressed in is recorded as sural nerve[20].
- RN7SKP98's expressed in is recorded as anterior cingulate cortex[21].