RN7SL263P
pseudogene in the species Homo sapiens
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RN7SL263P
Summary
RN7SL263P is a pseudogene[1].
Key Facts
- RN7SL263P's instance of is recorded as pseudogene[2].
- RN7SL263P's instance of is recorded as gene[3].
- RN7SL263P is a type of pseudogene[4].
- RN7SL263P's genomic start is recorded as 23261782[5].
- RN7SL263P's genomic end is recorded as 23262071[6].
- RN7SL263P's found in taxon is recorded as Homo sapiens[7].
- RN7SL263P's chromosome is recorded as human chromosome 22[8].
- RN7SL263P's strand orientation is recorded as reverse strand[9].
- RN7SL263P's exact match is recorded as http://identifiers.org/ncbigene/106480993[10].
- RN7SL263P's cytogenetic location is recorded as 22q11.23[11].
- RN7SL263P's expressed in is recorded as ganglionic eminence[12].
- RN7SL263P's expressed in is recorded as bone marrow cell[13].
- RN7SL263P's expressed in is recorded as ventricular zone[14].
- RN7SL263P's expressed in is recorded as epithelium of colon[15].
- RN7SL263P's expressed in is recorded as muscle of thigh[16].
- RN7SL263P's expressed in is recorded as monocyte[17].
- RN7SL263P's expressed in is recorded as blood[18].
- RN7SL263P's expressed in is recorded as gallbladder[19].
- RN7SL263P's expressed in is recorded as olfactory zone of nasal mucosa[20].
- RN7SL263P's expressed in is recorded as liver[21].