RN7SL598P
pseudogene in the species Homo sapiens
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RN7SL598P
Summary
RN7SL598P is a pseudogene[1].
Key Facts
- RN7SL598P's instance of is recorded as pseudogene[2].
- RN7SL598P's instance of is recorded as gene[3].
- RN7SL598P is a type of pseudogene[4].
- RN7SL598P's genomic start is recorded as 58179771[5].
- RN7SL598P's genomic end is recorded as 58180064[6].
- RN7SL598P's found in taxon is recorded as Homo sapiens[7].
- RN7SL598P's chromosome is recorded as human chromosome 14[8].
- RN7SL598P's strand orientation is recorded as forward strand[9].
- RN7SL598P's exact match is recorded as http://identifiers.org/ncbigene/106481759[10].
- RN7SL598P's cytogenetic location is recorded as 14q23.1[11].
- RN7SL598P's expressed in is recorded as testicle[12].
- RN7SL598P's expressed in is recorded as liver[13].
- RN7SL598P's expressed in is recorded as human kidney[14].
- RN7SL598P's expressed in is recorded as lung[15].
- RN7SL598P's expressed in is recorded as stomach[16].
- RN7SL598P's expressed in is recorded as superior frontal gyrus[17].
- RN7SL598P's expressed in is recorded as blood[18].
- RN7SL598P's expressed in is recorded as heart[19].
- RN7SL598P's expressed in is recorded as islet of Langerhans[20].
- RN7SL598P's expressed in is recorded as colon[21].