RN7SL616P
pseudogene in the species Homo sapiens
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RN7SL616P
Summary
RN7SL616P is a pseudogene[1].
Key Facts
- RN7SL616P's instance of is recorded as pseudogene[2].
- RN7SL616P's instance of is recorded as gene[3].
- RN7SL616P is a type of pseudogene[4].
- RN7SL616P's genomic start is recorded as 69478997[5].
- RN7SL616P's genomic end is recorded as 69479265[6].
- RN7SL616P's found in taxon is recorded as Homo sapiens[7].
- RN7SL616P's chromosome is recorded as human chromosome 5[8].
- RN7SL616P's strand orientation is recorded as reverse strand[9].
- RN7SL616P's exact match is recorded as http://identifiers.org/ncbigene/106481090[10].
- RN7SL616P's cytogenetic location is recorded as 5q13.2[11].
- RN7SL616P's expressed in is recorded as human kidney[12].
- RN7SL616P's expressed in is recorded as sural nerve[13].
- RN7SL616P's expressed in is recorded as stomach[14].
- RN7SL616P's expressed in is recorded as temporal lobe[15].
- RN7SL616P's expressed in is recorded as liver[16].
- RN7SL616P's expressed in is recorded as colon[17].
- RN7SL616P's expressed in is recorded as primary visual cortex[18].
- RN7SL616P's expressed in is recorded as islet of Langerhans[19].
- RN7SL616P's expressed in is recorded as gastrocnemius muscle[20].
- RN7SL616P's expressed in is recorded as monocyte[21].