RN7SL793P
pseudogene in the species Homo sapiens
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RN7SL793P
Summary
RN7SL793P is a pseudogene[1].
Key Facts
- RN7SL793P's instance of is recorded as pseudogene[2].
- RN7SL793P's instance of is recorded as gene[3].
- RN7SL793P is a type of pseudogene[4].
- RN7SL793P's genomic start is recorded as 102217318[5].
- RN7SL793P's genomic end is recorded as 102217613[6].
- RN7SL793P's found in taxon is recorded as Homo sapiens[7].
- RN7SL793P's chromosome is recorded as human chromosome 12[8].
- RN7SL793P's strand orientation is recorded as reverse strand[9].
- RN7SL793P's exact match is recorded as http://identifiers.org/ncbigene/106481137[10].
- RN7SL793P's cytogenetic location is recorded as 12q23.2[11].
- RN7SL793P's expressed in is recorded as muscle tissue[12].
- RN7SL793P's expressed in is recorded as testicle[13].
- RN7SL793P's expressed in is recorded as ganglionic eminence[14].
- RN7SL793P's expressed in is recorded as urinary bladder[15].
- RN7SL793P's expressed in is recorded as liver[16].
- RN7SL793P's expressed in is recorded as stromal cell of endometrium[17].
- RN7SL793P's expressed in is recorded as bone marrow[18].
- RN7SL793P's expressed in is recorded as primary visual cortex[19].
- RN7SL793P's expressed in is recorded as monocyte[20].
- RN7SL793P's expressed in is recorded as superior frontal gyrus[21].