RN7SL508P
pseudogene in the species Homo sapiens
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RN7SL508P
Summary
RN7SL508P is a pseudogene[1].
Key Facts
- RN7SL508P's instance of is recorded as pseudogene[2].
- RN7SL508P's instance of is recorded as gene[3].
- RN7SL508P is a type of pseudogene[4].
- RN7SL508P's genomic start is recorded as 118993857[5].
- RN7SL508P's genomic end is recorded as 118994159[6].
- RN7SL508P's found in taxon is recorded as Homo sapiens[7].
- RN7SL508P's chromosome is recorded as human chromosome 12[8].
- RN7SL508P's strand orientation is recorded as forward strand[9].
- RN7SL508P's exact match is recorded as http://identifiers.org/ncbigene/106481061[10].
- RN7SL508P's cytogenetic location is recorded as 12q24.23[11].
- RN7SL508P's expressed in is recorded as testicle[12].
- RN7SL508P's expressed in is recorded as muscle tissue[13].
- RN7SL508P's expressed in is recorded as liver[14].
- RN7SL508P's expressed in is recorded as corpus callosum[15].
- RN7SL508P's expressed in is recorded as human kidney[16].
- RN7SL508P's expressed in is recorded as primary visual cortex[17].
- RN7SL508P's expressed in is recorded as lymph node[18].
- RN7SL508P's expressed in is recorded as stomach[19].
- RN7SL508P's expressed in is recorded as monocyte[20].
- RN7SL508P's expressed in is recorded as olfactory zone of nasal mucosa[21].