RN7SL162P
pseudogene in the species Homo sapiens
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RN7SL162P
Summary
RN7SL162P is a pseudogene[1].
Key Facts
- RN7SL162P's instance of is recorded as pseudogene[2].
- RN7SL162P's instance of is recorded as gene[3].
- RN7SL162P is a type of pseudogene[4].
- RN7SL162P's genomic start is recorded as 28642979[5].
- RN7SL162P's genomic end is recorded as 28643270[6].
- RN7SL162P's found in taxon is recorded as Homo sapiens[7].
- RN7SL162P's chromosome is recorded as human chromosome 22[8].
- RN7SL162P's strand orientation is recorded as reverse strand[9].
- RN7SL162P's exact match is recorded as http://identifiers.org/ncbigene/106481828[10].
- RN7SL162P's cytogenetic location is recorded as 22q12.1[11].
- RN7SL162P's expressed in is recorded as testicle[12].
- RN7SL162P's expressed in is recorded as gonad[13].
- RN7SL162P's expressed in is recorded as lymph node[14].
- RN7SL162P's expressed in is recorded as primary visual cortex[15].
- RN7SL162P's expressed in is recorded as monocyte[16].
- RN7SL162P's expressed in is recorded as stromal cell of endometrium[17].
- RN7SL162P's expressed in is recorded as olfactory zone of nasal mucosa[18].
- RN7SL162P's expressed in is recorded as appendix[19].
- RN7SL162P's expressed in is recorded as liver[20].
- RN7SL162P's expressed in is recorded as smooth muscle tissue[21].