RN7SL66P
pseudogene in the species Homo sapiens
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RN7SL66P
Summary
RN7SL66P is a pseudogene[1].
Key Facts
- RN7SL66P's instance of is recorded as pseudogene[2].
- RN7SL66P's instance of is recorded as gene[3].
- RN7SL66P is a type of pseudogene[4].
- RN7SL66P's genomic start is recorded as 10280628[5].
- RN7SL66P's genomic end is recorded as 10280891[6].
- RN7SL66P's found in taxon is recorded as Homo sapiens[7].
- RN7SL66P's chromosome is recorded as human chromosome 2[8].
- RN7SL66P's strand orientation is recorded as forward strand[9].
- RN7SL66P's exact match is recorded as http://identifiers.org/ncbigene/106480485[10].
- RN7SL66P's cytogenetic location is recorded as 2p25.1[11].
- RN7SL66P's expressed in is recorded as sural nerve[12].
- RN7SL66P's expressed in is recorded as testicle[13].
- RN7SL66P's expressed in is recorded as bone marrow[14].
- RN7SL66P's expressed in is recorded as superior frontal gyrus[15].
- RN7SL66P's expressed in is recorded as liver[16].
- RN7SL66P's expressed in is recorded as stromal cell of endometrium[17].
- RN7SL66P's expressed in is recorded as gallbladder[18].
- RN7SL66P's expressed in is recorded as monocyte[19].
- RN7SL66P's expressed in is recorded as islet of Langerhans[20].
- RN7SL66P's expressed in is recorded as blood[21].