RN7SL299P
pseudogene in the species Homo sapiens
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RN7SL299P
Summary
RN7SL299P is a pseudogene[1].
Key Facts
- RN7SL299P's instance of is recorded as pseudogene[2].
- RN7SL299P's instance of is recorded as gene[3].
- RN7SL299P is a type of pseudogene[4].
- RN7SL299P's genomic start is recorded as 232222866[5].
- RN7SL299P's genomic end is recorded as 232223145[6].
- RN7SL299P's found in taxon is recorded as Homo sapiens[7].
- RN7SL299P's chromosome is recorded as human chromosome 1[8].
- RN7SL299P's strand orientation is recorded as forward strand[9].
- RN7SL299P's exact match is recorded as http://identifiers.org/ncbigene/106479331[10].
- RN7SL299P's cytogenetic location is recorded as 1q42.2[11].
- RN7SL299P's expressed in is recorded as human kidney[12].
- RN7SL299P's expressed in is recorded as liver[13].
- RN7SL299P's expressed in is recorded as gallbladder[14].
- RN7SL299P's expressed in is recorded as blood[15].
- RN7SL299P's expressed in is recorded as monocyte[16].
- RN7SL299P's expressed in is recorded as endometrium[17].
- RN7SL299P's expressed in is recorded as prefrontal cortex[18].
- RN7SL299P's expressed in is recorded as muscle of leg[19].
- RN7SL299P's expressed in is recorded as gastrocnemius muscle[20].
- RN7SL299P's expressed in is recorded as left coronary artery[21].