RN7SKP5
pseudogene in the species Homo sapiens
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RN7SKP5
Summary
RN7SKP5 is a pseudogene[1].
Key Facts
- RN7SKP5's instance of is recorded as pseudogene[2].
- RN7SKP5's instance of is recorded as gene[3].
- RN7SKP5 is a type of pseudogene[4].
- RN7SKP5's genomic start is recorded as 46249942[5].
- RN7SKP5's genomic end is recorded as 46250213[6].
- RN7SKP5's found in taxon is recorded as Homo sapiens[7].
- RN7SKP5's chromosome is recorded as human chromosome 13[8].
- RN7SKP5's strand orientation is recorded as forward strand[9].
- RN7SKP5's exact match is recorded as http://identifiers.org/ncbigene/100873849[10].
- RN7SKP5's cytogenetic location is recorded as 13q14.13[11].
- RN7SKP5's expressed in is recorded as corpus callosum[12].
- RN7SKP5's expressed in is recorded as lymph node[13].
- RN7SKP5's expressed in is recorded as C1 segment[14].
- RN7SKP5's expressed in is recorded as white blood cell[15].
- RN7SKP5's expressed in is recorded as right uterine tube[16].
- RN7SKP5's expressed in is recorded as gallbladder[17].
- RN7SKP5's expressed in is recorded as prefrontal cortex[18].
- RN7SKP5's expressed in is recorded as bone marrow[19].
- RN7SKP5's expressed in is recorded as appendix[20].
- RN7SKP5's expressed in is recorded as primary visual cortex[21].