RN7SL268P
pseudogene in the species Homo sapiens
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RN7SL268P
Summary
RN7SL268P is a pseudogene[1].
Key Facts
- RN7SL268P's instance of is recorded as pseudogene[2].
- RN7SL268P's instance of is recorded as gene[3].
- RN7SL268P is a type of pseudogene[4].
- RN7SL268P's genomic start is recorded as 23879493[5].
- RN7SL268P's genomic end is recorded as 23879790[6].
- RN7SL268P's found in taxon is recorded as Homo sapiens[7].
- RN7SL268P's chromosome is recorded as human chromosome 22[8].
- RN7SL268P's strand orientation is recorded as reverse strand[9].
- RN7SL268P's exact match is recorded as http://identifiers.org/ncbigene/106479319[10].
- RN7SL268P's cytogenetic location is recorded as 22q11.23[11].
- RN7SL268P's expressed in is recorded as right hemisphere of cerebellum[12].
- RN7SL268P's expressed in is recorded as testicle[13].
- RN7SL268P's expressed in is recorded as pituitary gland[14].
- RN7SL268P's expressed in is recorded as bone marrow cell[15].
- RN7SL268P's expressed in is recorded as body of pancreas[16].
- RN7SL268P's expressed in is recorded as anterior pituitary[17].
- RN7SL268P's expressed in is recorded as primary visual cortex[18].
- RN7SL268P's expressed in is recorded as apex of heart[19].
- RN7SL268P's expressed in is recorded as left ventricle[20].
- RN7SL268P's expressed in is recorded as right lobe of thyroid gland[21].