RN7SL789P
pseudogene in the species Homo sapiens
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RN7SL789P
Summary
RN7SL789P is a pseudogene[1].
Key Facts
- RN7SL789P's instance of is recorded as pseudogene[2].
- RN7SL789P's instance of is recorded as gene[3].
- RN7SL789P is a type of pseudogene[4].
- RN7SL789P's genomic start is recorded as 32655016[5].
- RN7SL789P's genomic end is recorded as 32655308[6].
- RN7SL789P's found in taxon is recorded as Homo sapiens[7].
- RN7SL789P's chromosome is recorded as human chromosome 19[8].
- RN7SL789P's strand orientation is recorded as reverse strand[9].
- RN7SL789P's exact match is recorded as http://identifiers.org/ncbigene/106479508[10].
- RN7SL789P's cytogenetic location is recorded as 19q13.11[11].
- RN7SL789P's expressed in is recorded as testicle[12].
- RN7SL789P's expressed in is recorded as skeletal muscle tissue[13].
- RN7SL789P's expressed in is recorded as bone marrow[14].
- RN7SL789P's expressed in is recorded as monocyte[15].
- RN7SL789P's expressed in is recorded as bone marrow cell[16].
- RN7SL789P's expressed in is recorded as stromal cell of endometrium[17].
- RN7SL789P's expressed in is recorded as tonsil[18].
- RN7SL789P's expressed in is recorded as liver[19].
- RN7SL789P's expressed in is recorded as primary visual cortex[20].
- RN7SL789P's expressed in is recorded as urinary bladder[21].