RN7SL292P
pseudogene in the species Homo sapiens
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RN7SL292P
Summary
RN7SL292P is a pseudogene[1].
Key Facts
- RN7SL292P's instance of is recorded as pseudogene[2].
- RN7SL292P's instance of is recorded as gene[3].
- RN7SL292P is a type of pseudogene[4].
- RN7SL292P's genomic start is recorded as 51716657[5].
- RN7SL292P's genomic end is recorded as 51716922[6].
- RN7SL292P's found in taxon is recorded as Homo sapiens[7].
- RN7SL292P's chromosome is recorded as human chromosome 7[8].
- RN7SL292P's strand orientation is recorded as forward strand[9].
- RN7SL292P's exact match is recorded as http://identifiers.org/ncbigene/106481002[10].
- RN7SL292P's cytogenetic location is recorded as 7p12.1[11].
- RN7SL292P's expressed in is recorded as gonad[12].
- RN7SL292P's expressed in is recorded as ventricular zone[13].
- RN7SL292P's expressed in is recorded as liver[14].
- RN7SL292P's expressed in is recorded as monocyte[15].
- RN7SL292P's expressed in is recorded as myometrium[16].
- RN7SL292P's expressed in is recorded as gastrocnemius muscle[17].
- RN7SL292P's expressed in is recorded as superior frontal gyrus[18].
- RN7SL292P's expressed in is recorded as blood[19].
- RN7SL292P's expressed in is recorded as prefrontal cortex[20].
- RN7SL292P's expressed in is recorded as stomach[21].