RN7SL582P
pseudogene in the species Homo sapiens
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RN7SL582P
Summary
RN7SL582P is a pseudogene[1].
Key Facts
- RN7SL582P's instance of is recorded as pseudogene[2].
- RN7SL582P's instance of is recorded as gene[3].
- RN7SL582P is a type of pseudogene[4].
- RN7SL582P's genomic start is recorded as 116582552[5].
- RN7SL582P's genomic end is recorded as 116582830[6].
- RN7SL582P's found in taxon is recorded as Homo sapiens[7].
- RN7SL582P's chromosome is recorded as human chromosome 3[8].
- RN7SL582P's strand orientation is recorded as reverse strand[9].
- RN7SL582P's exact match is recorded as http://identifiers.org/ncbigene/106479435[10].
- RN7SL582P's cytogenetic location is recorded as 3q13.31[11].
- RN7SL582P's expressed in is recorded as epithelium of colon[12].
- RN7SL582P's expressed in is recorded as testicle[13].
- RN7SL582P's expressed in is recorded as ventricular zone[14].
- RN7SL582P's expressed in is recorded as white blood cell[15].
- RN7SL582P's expressed in is recorded as corpus callosum[16].
- RN7SL582P's expressed in is recorded as ectocervix[17].
- RN7SL582P's expressed in is recorded as monocyte[18].
- RN7SL582P's expressed in is recorded as human kidney[19].
- RN7SL582P's expressed in is recorded as liver[20].
- RN7SL582P's expressed in is recorded as sural nerve[21].